| Type | Gene1 | Effect | Gene2 | Sentence | MedLine Reference | Time of Interaction in evidence | # of References | territories of interaction | Evidence for Direct | Last author | Journal | Year | start page | end page |
| Expression | activin | positive | chd | Since activin is known to induce chordin transcription (Sasai et al., 1994), we tested whether Chordin was required for the dorsalization of animal cap explants by activin. | 2 | 2 | Public | positive | ||||||
| Expression | activin | positive | fgf8a | We demonstrate that transcription of fgf8a is induced by activin and the fgf8a protein inhibits the expression of nodal and pitx2a and leads to expression of the chicken snail related gene (cSnR) [9]. | 10074453:7 | 2 | 3 | Public | positive | |||||
| Expression | activin | positive | gata5 | Injection of RNA encoding a constitutively active activin receptor leads to ectopic expression of gata5 and ntl. gata5 is activated cell-autonomously, whereas ntl is induced in cells distant from those which have received the RNA, showing that although ex | 10375499:6 | 2 | 1 | Public | positive | |||||
| Expression | activin | positive | gsc | In these cells, activin rapidly induces the expression of the immediate early response genes goosecoid and no tail. | 10349616:2 | 2 | 10 | Public | positive | |||||
| Expression | activin | positive | lhx1a | In this study, we report studies on the mechanism of regulation of the Lim-1 gene by activin/nodal signals and the role of FAST-1/FoxH1 in this process. | 2 | 5 | Public | positive | ||||||
| Expression | activin | positive | myf5 | activin treatment induced the expression of the somite marker genes Myf5 and Actin and the pan-neural marker NCAM. | 2 | 1 | Public | positive | ||||||
| Regulation | activin | positive | ntl | In Xenopus animal caps, Acti vin can induce gsc at high concentrations and Brachyury ( Xbra ), a marker for the notochord and posterior mesoderm, at lo wer concentrations (Green et al., 1997). | 2 | 6 | Public | positive | ||||||
| Expression | activin | positive | pitx2a | In contrast, both Xnr1 and activin injection resulted in strong acti v ation of pitx2a transcription in animal cap e xplants (Fig. 7), in agreement with the results obtained in injected whole embryos (Fig. 6B,C). | 2 | 1 | Public | positive | ||||||
| Expression | activin | positive | smad2 | Furthermore, although Madr2 remains unlocalized in ectodermal explants, addition of activin enhances the concentration of Madr2 in the nucleus. | 8756346:4 | 2 | 3 | Public | positive | |||||
| Expression | activin | positive | tbx6 | Second, the mesoderm-inducing factors activin and bFGF activate tbx6 expression in animal caps. | 9119115:4 | 2 | 2 | Public | positive | |||||
| Binding | activin | neutral | acvr2a | Inhibin also binds to ActRII through its beta subunit, competes with the binding of activin to ActRII, but fails to form the ActRII.SKR2 complex. | 7890768:6 | 2 | 20 | Public | HepG 2 | |||||
| Binding | activin | neutral | acvr2a | Inhibin also binds to ActRII through its beta subunit, competes with the binding of activin to ActRII, but fails to form the ActRII.SKR2 complex. | 7890768:6 | 2 | 20 | Public | HepG 2 | |||||
| Binding | activin | neutral | bmp2a | In this study, we have exploited the well characterized model of Xenopus mesoderm induction to determine the intracellular interactions between BMP-2/4 and activin/BVg1 signaling cascades. | 9409665:3 | 2 | 3 | Public | ||||||
| Binding | activin | neutral | bmp3 | A role for a BMP ligand acting as a BMP antagonist has been reported for the more distantly related BMP3, which binds to the BMP and activin receptor ActRII without activating it, thus acting as a receptor inhibitor (Daluiski et al., 2001 and Gamer et al. | 2 | 1 | Public | |||||||
| Binding | activin | neutral | bmp7 | BMP-7 can interact with activin type I and type II receptors in addition to BMP-2/BMP-4 receptors ( 26 , 28 ). | 9268344:10043 | 2 | 5 | Public | ||||||
| Binding | activin | neutral | foxh1 | This motif is also located within the SID domain of FoxH1 and is conserved in all family members, suggestingthat this region may also be critical for FoxH1 association with the TGF?/activin regulated Smads. | 2 | 4 | Public | |||||||
| Binding | activin | neutral | fsta | Follistatin (FS) binds activin and inhibin proteins. | 9858480:0 | 2 | 86 | Public | Hs | |||||
| Expression | activin | neutral | gsc | Goosecoid is a homeobox gene that is expressed as an immediate early response to mesoderm induction by activin. | 8734495:0 | 2 | 1 | Public | unknown | |||||
| Binding | activin | neutral | nog1 | Furthermore, their binding to BMP-2 differs from the binding mode established for noggin/BMP7 or follistatin/activin interaction. | 2 | 2 | Public | |||||||
| Binding | activin | neutral | smad | The FAST/Smad complex binds to activin/nodal responsive elements (ARE/NRE) and activates homeobox genes implicated in mesoderm induction in both Xenopus and mouse (reviewed in Massague and Wotton, 2000). | 2 | 1 | Public | |||||||
| Binding | activin | neutral | smad2 | A paradigm of Smad–cofactor interaction was established for TGF-?/activin signaling by the identification of winged helix proteins, such as FAST-1 as DNA-binding partners that interact with Smad2/3 at target promoters (14,15). | 2 | 1 | Public | |||||||
| Binding | activin | neutral | smad3a | Among them, Smad3 is shown to transiently associate with activin type IB and TGF-eta type I receptor and to be phosphorylated by the type I receptors to propagate downstream signaling ( 29 ). | 10681527:10154 | 2 | 3 | Public | ||||||
| Binding | activin | neutral | tgfb1 | Ongoing experiments will explore the nature of the interaction between activin and TGF-beta in detail, by testing some of these hypotheses. | 9275089:10280 | 2 | 2 | Public | ||||||
| Binding | activin | neutral | wnt | Melton, Interaction of Wnt and activin in dorsal mesoderm induction in Xenopus. | 2 | 3 | Public | |||||||
| Expression | acvr1 | positive | bmp2a | Since Bmps act as negative regulators of chordin expression (Schulte-Merker et al., 1998), and CA and KM Alk8 affect the expression of bmps2b and -4, it is expected that chordin expression would also be affected. | 2 | 2 | Public | positive | ||||||
| Expression | acvr1 | positive | bmp2b | injected mRNA encoding a constitutively active version of Alk8 can rescue the strong dorsalization of bmp2b/swirl mutants. | overexpression | 4.66 | mesendoderm | blastoderm | 2 | Hammerschmidt, M. | Development | 2001 | 128 | 849 |
| Regulation | acvr1 | positive | bmp4 | A constitutively active Alk8-TGFbeta-receptor can ectopically induce bmp2b and bmp4 and rescues the dorsalization of MZspg. | 16775002:9 | 2 | 1 | Public | zygote | positive | ||||
| Expression | acvr1 | positive | bmp4 | This indicates that pou2 acts upstream of Alk8, a maternally provided receptor implicated in the activation of zygotic bmp2b and bmp4 transcription. | 16775002:10 | 2 | 16 | Public | zygote | positive | ||||
| Expression | acvr1 | positive | bmp7 | injected mRNA encoding a constitutively active version of Alk8 can rescue the strong dorsalization of bmp7/snailhouse mutants | overexpression | 4.66 | mesendoderm | blastoderm | 2 | Hammerschmidt, M. | Development | 2001 | 128 | 849 |
| Regulation | acvr1 | positive | bre | Furthermore, Smad7 inhibited the expression of the BMP-responsive reporter BRE-Luc (18) induced by the constitutively active forms of BMPRIA, BMPRIB, acvrl1, and ALK2 (Fig. 1B). | 2 | 4 | Public | positive | ||||||
| Expression | acvr1 | positive | bre | Furthermore, Smad7 inhibited the expression of the BMP-responsive reporter BRE-Luc (18) induced by the constitutively active forms of BMPRIA, BMPRIB, acvrl1, and ALK2 (Fig. 1B). | 2 | 4 | Public | positive | ||||||
| Expression | acvr1 | positive | chd | By early somite stages, CA Alk8 expressing embryos exhibit reduced chordin expression in diminished anterior neural structures and in the ventral tailbud (Fig. 2U,U'). | 2 | 2 | Public | positive | ||||||
| Expression | acvr1 | positive | dlx3b | in alk8 (a type I TGFbeta receptor) MO-injected embryos, vhnf1 expression in the endoderm is significantly reduced. | mutant embryos | 8 | epiblast | ectoderm | 1 | Mary C. Mullins | Development | 2001 | 128 | 859 |
| Expression | acvr1 | positive | foxa3 | Decrease of Bmp activity by alk8 morpholino injection caused a change of foxa3 expression pattern. | 2 | 1 | Public | positive | ||||||
| Expression | acvr1 | positive | gata2 | the data suggest that Alk8 acts as a Bmp2b/7 receptor upstream of Smad5. | mutant embryos | 8 | epiblast | ectoderm | 1 | Mary C. Mullins | Development | 2001 | 128 | 859 |
| Expression | acvr1 | positive | hnf1b | Ved expression is up-regulated during gastrulation in MZ-laf/bmpRI signaling mutants. | MASO | 24 | gut | gut | 3 | Lin, S. | Dev Biol | 2007 | 303 | 561 |
| Expression | acvr1 | positive | myod1 | CA Alk8 expressing embryos often display an interrupted myoD expression pattern, where adaxial cells appaear fused, forming a loop toward the posterior end. | 2 | 2 | Public | positive | ||||||
| Expression | acvr1 | positive | otx2 | At 80% epiboly, CA Alk8 expressing embryos exhibit restricted dorsal anterior otx2 expression (Fig. 5C,C'), while KM Alk8 expressing embryos exhibit up regulated midline and lateral expansion of otx2 expression (Fig. 5A,A'). | 2 | 2 | Public | positive | ||||||
| Expression | acvr1 | positive | smad5 | The ability of sbn/Smad5 mutants to block the ventralizing activities of CA alk8 demonstrate that alk8 functions upstream of the Smad5 transcription factor, and suggests that Smad5 is required in alk8 signaling pathways. | 2 | 2 | Public | positive | ||||||
| Expression | acvr1 | positive | smad5 | In most MZ-laf/alk8 mutants dlx3 expression is absent. | MASO | 4.66 | mesendoderm | blastoderm | 1, 2 | Hammerschmidt, M. | Development | 2001 | 128 | 849 |
| Expression | acvr1 | positive | spi1 | Ved expression is up-regulated during gastrulation in MZ-laf/bmpRI signaling mutants. | mutant embryos | 11.66 | lateral plate mesoderm | lateral plate mesoderm | 1 | Lieschke, G. J. | Curr Biol | 2006 | 16 | 506 |
| ProtModification | acvr1 | phosphorylation | smad1 | B, in vitro phosphorylation of Smad1 by ALK2. | 9748228:10235 | 2 | 15 | Public | HepG 2 | unknown | ||||
| ProtModification | acvr1 | phosphorylation | smad1 | The activated BMP type I receptors acvrl1, ALK2, ALK3 and ALK6 phosphorylate downstream target Smads 1/5/8 ([Heldin et al., 1997] and [Massague and Wotton, 2000]) which then bind to Smad4, migrate to the nucleus and regulate transcription of target genes | 2 | 4 | Public | unknown | ||||||
| ProtModification | acvr1 | phosphorylation | smad5 | When stimulated by Bmp7, Alk2 recognizes and phosphorylates Smad1, and also phosphorylates Smad5 and Smad8 ( Macias-Silva et al., 1998). | 2 | 7 | Public | unknown | ||||||
| ProtModification | acvr1 | phosphorylation | smad8 | Constitutively active BMP type I receptors, ALK-3 and ALK-6, as well as ALK-2, were phosphorylated Smad8 and induced Smad8 interaction with Smad4. | 10814522:3 | 2 | 8 | Public | COS I | osteoblast | unknown | |||
| Expression | acvr1 | neutral | bmp4 | Together, these results show that Mrdr and alk8 strongly interact to positively regulate the onset of bmp2b/4 expression. | 2 | 3 | Public | unknown | ||||||
| Binding | acvr1 | neutral | bmp7 | OP-1 bound to ALK-2 and ALK-6 efficiently, and to ALK-3 less efficiently, whereas BMP-4 bound to ALK-3 and ALK-6 efficiently. | 8006002:6 | 2 | 21 | Public | COS | osteoblast | ||||
| Expression | acvr1 | neutral | bre | Furthermore, Smad7 inhibited the expression of the BMP-responsive reporter BRE-Luc (18) induced by the constitutively active forms of BMPRIA, BMPRIB, acvrl1, and ALK2 (Fig. 1B). | 2 | 4 | Public | unknown | ||||||
| Expression | acvr1 | neutral | chd | By early somite stages, CA Alk8 expressing embryos exhibit reduced chordin expression in diminished anterior neural structures and in the ventral tailbud (Fig. 2U,U'). | 2 | 2 | Public | unknown | ||||||
| Expression | acvr1 | neutral | myod1 | KM Alk8 expression results in embryos exhibiting normal adaxial myoD expression along a broadened midline and thickened somitic myoD expression. | 2 | 2 | Public | unknown | ||||||
| Expression | acvr1 | neutral | otx2 | At 80% epiboly, CA Alk8 expressing embryos exhibit restricted dorsal anterior otx2 expression (Fig. 5C,C'), while KM Alk8 expressing embryos exhibit up regulated midline and lateral expansion of otx2 expression (Fig. 5A,A'). | 2 | 2 | Public | unknown | ||||||
| Binding | acvr1 | neutral | smad1 | A, ALK2 interacts with Smad1. | 9748228:10229 | 2 | 6 | Public | ||||||
| Binding | acvr1 | neutral | smad4 | The activated BMP type I receptors acvrl1, ALK2, ALK3 and ALK6 phosphorylate downstream target Smads 1/5/8 ([Heldin et al., 1997] and [Massague and Wotton, 2000]) which then bind to Smad4, migrate to the nucleus and regulate transcription of target genes | 2 | 6 | Public | |||||||
| Binding | acvr1 | neutral | smurf2 | In addition, Smurf1 associates with transforming growth factor-beta type I receptor through the inhibitory Smad (I-Smad) Smad7 and induces their degradation. | 12857866:1 | 2 | 11 | Public | ||||||
| Binding | acvr1 | neutral | tgfb1 | When coexpressed with the type II receptors of TGF-eta and activin, ALK-2 was shown to be able to form a heteromeric complex with TGF-eta and activin, respectively ( 7-9 ). | 9371779:10208 | 2 | 5 | Public | nmumg | |||||
| Expression | acvr1 | negative | bmp4 | In contrast, KM Alk8 down regulates ventral bmp2b expression in shield stage embryos (data not shown). | 2 | 2 | Public | negative | ||||||
| Expression | acvr1 | negative | chd | Ectopic expression of CA Alk8 reduces chordin expression in shield and 80% epiboly stage embryos (Fig. 2O,R), while KM Alk8 expands chordin expression (Fig. 2M,P). | 2 | 2 | Public | negative | ||||||
| Expression | acvr1 | negative | foxb1.2 | the data suggest that Alk8 acts as a Bmp2b/7 receptor upstream of Smad5. | mutant embryos | 8 | epiblast | ectoderm | 1 | Mary C. Mullins | Development | 2001 | 128 | 859 |
| Expression | acvr1 | negative | ins | Embryos injected with alk8 morpholino exhibited remarkably reduced insulin expression (Fig. 8F). | 2 | 1 | Public | negative | ||||||
| Expression | acvr1 | negative | otx2 | Otx2 expression is reduced by CA Alk8 and expanded by KM Alk8, demonstrating a respective loss and expansion of prospective neural tissue that is appaarent at very early stages of development. | 2 | 2 | Public | negative | ||||||
| Expression | acvr1 | negative | ved | Foxb1.2 expression is expanded ventrally in MZ-laf embryos at 70% epiboly, the expansion is more pronounced in more vegetal regions. | mutant embryos | 4.66 | EVL | blastoderm | 1 | Franco Cotelli | Developmental Dynamics | 2004 | 230 | 494 |
| Binding | acvr1b | neutral | acvr2a | If cotransfected with ActRII/IIB and ALK4, Cripto inhibited crosslinking of activin to ALK4 and the association of ALK4 with ActRII/IIB. | 12682303:6 | 2 | 13 | Public | nmumg | keratinocyte | ||||
| Binding | acvr1b | neutral | acvr2a | If cotransfected with ActRII/IIB and ALK4, Cripto inhibited crosslinking of activin to ALK4 and the association of ALK4 with ActRII/IIB. | 12682303:6 | 2 | 13 | Public | nmumg | keratinocyte | ||||
| Expression | acvr1b | positive | ntl | Injection of TARAM-A* (acvr1b) induced very robust expression of ntl in large patches of cells. | overexpression | 4.33 | margin | margin | 2 | Thierry Lepage | Development | 2002 | 129 | 4901 |
| Expression | acvr1b | positive | og9x | Injection of TARAM-A*(acvr1b) induced very robust expression of casanova (sox32) in large patches of cells. | overexpression | 5.25 | margin | margin | 2 | Thierry Lepage | Development | 2002 | 129 | 4901 |
| Expression | acvr1b | positive | pitx2a | We report here that similar to effects of ectopic TGF betas, right-side expression of constitutively active activin-like kinase (ALK) 4 results in LR organ reversals as well as altered pitx2a expression in the lateral plate mesoderm. | 15063168:2 | 2 | 3 | Public | LR | cardiomyocyte | positive | |||
| ProtModification | acvr1b | phosphorylation | smad | The binding of Nodal to its receptor complex (Alk4/ActRIIB/co-receptor EGF-CFC) activates Smad2/3, and phosphorylation of these Smads by Alk4 increases their affinity for Smad4. | 2 | 1 | Public | unknown | ||||||
| Binding | acvr1b | neutral | smad | The ?4-?5 loop of TaramA, a Smad interacting domain, is identical to that of Alk4 ( ten Dijke et al., 1994b), suggesting that TaramA and Alk4 may interact with similar downstream Smad molecules and may perform similar functions.When CA alk8 and taramA* RN | 2 | 2 | Public | |||||||
| ProtModification | acvr1b | phosphorylation | smad2 | This suggests that Smad2 and Smad3 association with ALK4 is an early event after receptor heteromerization, in activin signaling. | 9892009:1092 | 2 | 5 | Public | 293 | unknown | ||||
| Expression | acvr1b | positive | smad2 | Ca-ALK4 induced a strong nuclear accumulation of EGFP-Smad2 during the 20 min washout period, and this was completely abolished by the treatment with AA (Figure 4A). | 2 | 1 | Public | positive | ||||||
| ProtModification | acvr1b | phosphorylation | smad3a | ALK4 is a Ser/Thr kinase that phosphorylates cytoplasmic Smad2 and Smad3 ( Massague and W otton, 2000 ). | 2 | 6 | Public | unknown | ||||||
| Binding | acvr1b | neutral | smad3a | Nevertheless, when cells were stimulated by activin, the amount of Smad3 associated with ALK4 increases. | 9892009:1073 | 2 | 3 | Public | ||||||
| Expression | acvr1b | positive | sox17 | Similarly, whereas injection of very low doses 1-2 pg of tar*/acvr1b caused the ectopic expression of sox17 in about 32% of the embryos, treatment with SU5402 following the injection increased this percentage to 54% (Table 1). | 2 | 9 | Public | positive | ||||||
| Expression | acvr1b | positive | sox17 | Injection of TARAM-A* induced very robust expression of sox17, ntl,og9x, bon/mixer and casanova in large patches of cells. | overexpression | 4.33 | margin | margin | 2 | Thierry Lepage | Development | 2002 | 129 | 4901 |
| Expression | acvr1b | positive | sox32 | Embryo injected at the eight-cell stage into one blastomere with 40 pg of TARAM-A*(acvr1b) and with 100 pg of mRNA encoding a nuclear b-Gal (blue colour) as a lineage tracer. TARAM-A*(acvr1b) induces confluent patches of mezzo (og9x)-expressing cells. | overexpression | 4.33 | margin | margin | 2 | Thierry Lepage | Development | 2002 | 129 | 4901 |
| Regulation | acvr1b | unknown | tgfb1 | This phenomenon was also observed in MZoep mutant embryos treated with the small compound SB431542 (39), which specifically inhibits ALK4/5/7-mediated TGF-? signaling. | 2 | 1 | Public | unknown | ||||||
| Binding | acvr1b | neutral | tgfb1 | Together, these results suggest not only that ALK4 interacts with multiple TGF?s to generate embryonic pattern, but also that ALK4 ligands differentially utilize the ALK4 pathway to regulate distinct aspects of axial pattern, with Vg1 as a modulator of AL | 2 | 1 | Public | |||||||
| ProtModification | acvr1b | phosphorylation | ttrap | ALK4 phosphorylated TTRAP in vitro (Fig. 6A). | 2 | 1 | Public | unknown | ||||||
| Binding | acvr1b | neutral | ttrap | Weobserved binding of Alk4 to TTRAP (Fig. 5D). | 2 | 1 | Public | |||||||
| Binding | acvr2b | neutral | bmp2a | Consistent with previous observations on the Drosophila type II receptor, punt ( 56 ), we were unable to observe any binding of BMP-2 to ActRII (Fig. 7 A , lane 8 ) or ActRIIB (data not shown) when these receptors were expressed alone. | 9872992:10251 | 2 | 5 | Public | ||||||
| Binding | acvr2b | neutral | bmpr1a | Moreover, ActRIIB can recruit both Alk4 for activin-like signaling and Alk3 for BMP-like signaling (Massague and Chen 2000 ). | 3240211037 | 2 | 2 | Public | ||||||
| Regulation | acvr2b | negative | lft2 | Similarly, the effects of Antivin and Lefty2 can be suppressed by overexpression of the nodal-related genes cyclops and squint or the extracellular domain of ActRIIB. | 10518210:4 | 2 | 8 | Public | negative | |||||
| Regulation | acvrl1 | positive | bre | Furthermore, Smad7 inhibited the expression of the BMP-responsive reporter BRE-Luc (18) induced by the constitutively active forms of BMPRIA, BMPRIB, acvrl1, and ALK2 (Fig. 1B). | 2 | 4 | Public | positive | ||||||
| Expression | acvrl1 | neutral | bre | Furthermore, Smad7 inhibited the expression of the BMP-responsive reporter BRE-Luc (18) induced by the constitutively active forms of BMPRIA, BMPRIB, acvrl1, and ALK2 (Fig. 1B). | 2 | 4 | Public | unknown | ||||||
| Expression | acvrl1 | positive | bre | Furthermore, Smad7 inhibited the expression of the BMP-responsive reporter BRE-Luc (18) induced by the constitutively active forms of BMPRIA, BMPRIB, acvrl1, and ALK2 (Fig. 1B). | 2 | 4 | Public | positive | ||||||
| Regulation | acvrl1 | positive | smad1 | TGF-beta/acvrl1-induced Smad1/5 phosphorylation in ECs occurs transiently. | 16571110:3 | 2 | 20 | Public | ec | positive | ||||
| ProtModification | acvrl1 | phosphorylation | smad1 | The activated BMP type I receptors acvrl1, ALK2, ALK3 and ALK6 phosphorylate downstream target Smads 1/5/8 ([Heldin et al., 1997] and [Massague and Wotton, 2000]) which then bind to Smad4, migrate to the nucleus and regulate transcription of target genes | 2 | 5 | Public | unknown | ||||||
| Binding | acvrl1 | neutral | smad1 | For the interaction of Smad1 with ALK-1 or ALK-2 not only the L3 loop is required, but also the alpha-helix 1 (H1) in MH2 domain [ 22 ]. | 11106403:10085 | 2 | 5 | Public | ||||||
| Binding | acvrl1 | neutral | smad4 | The activated BMP type I receptors acvrl1, ALK2, ALK3 and ALK6 phosphorylate downstream target Smads 1/5/8 ([Heldin et al., 1997] and [Massague and Wotton, 2000]) which then bind to Smad4, migrate to the nucleus and regulate transcription of target genes | 2 | 6 | Public | |||||||
| ProtModification | acvrl1 | phosphorylation | smad5 | The activated BMP type I receptors acvrl1, ALK2, ALK3 and ALK6 phosphorylate downstream target Smads 1/5/8 ([Heldin et al., 1997] and [Massague and Wotton, 2000]) which then bind to Smad4, migrate to the nucleus and regulate transcription of target genes | 2 | 5 | Public | unknown | ||||||
| ProtModification | acvrl1 | phosphorylation | smad8 | The activated BMP type I receptors acvrl1, ALK2, ALK3 and ALK6 phosphorylate downstream target Smads 1/5/8 ([Heldin et al., 1997] and [Massague and Wotton, 2000]) which then bind to Smad4, migrate to the nucleus and regulate transcription of target genes | 2 | 5 | Public | unknown | ||||||
| Regulation | acvrl1 | unknown | tgfb1 | Endothelial TGF-beta pathways, mediated by acvrl1 and ALK5, are impaired in HHT cells. | 15993872:5 | 2 | 11 | Public | unknown | |||||
| Expression | acvrl1 | positive | tlx2 | Expression of activated acvrl1 in P19 cells induced the Tlx2 promoter to a level similar to that observed for ALK2 (Fig. 8 B ), whereas activated acvrl1 was unable to induce the activin-responsive reporter gene, pA3-lux (data not shown). | 9748228:10259 | 2 | 2 | Public | positive | |||||
| Expression | bmp2a | negative | acvr1b | overexpression of BMPs compromises endoderm formation, formation of endoderm precursors is negatively regulated by BMPs on the ventral side. | overexpression | 5.25 | mesendoderm | blastoderm | 2 | Thierry Lepage | Development | 2006 | 133 | 2189 |
| Expression | bmp2a | negative | ndr1 | In embryos in which Bmp signaling was blocked at 18 hpf, gata4 and gata6 expression was greatly reduced in the liver region at 29-30 hpf. | overexpression | 8 | margin | margin | 2 | Hammerschmidt, M. | Curr Biol | 2007 | 17 | 475 |
| Expression | bmp2b | negative | acvr1b | We never found a homozygous laftm110b embryo that had a wild-type or ventralized phenotype, consistent with the Laf/Alk8 receptor functioning downstream of the Bmp2b. | overexpression | 5.25 | mesendoderm | blastoderm | 2 | Thierry Lepage | Development | 2006 | 133 | 2189 |
| Expression | bmp2b | negative | ndr1 | Ved expression domain expanded to the dorsal margin in bmp2b RNA-injected embryos at the 80% epiboly stage. | overexpression | 8 | margin | margin | 2 | Hammerschmidt, M. | Curr Biol | 2007 | 17 | 475 |
| Regulation | bmp7 | positive | acvr1 | OP-1 alone increased ActR-I, BMPR-IA, and BMPR-II mRNA levels, but did not change the BMPR-IB level. | 9322928:10188 | 2 | 4 | Public | positive | |||||
| Expression | bmp7 | negative | acvr1b | Prdm1 expression is reduced in snh (BMP7) mutant embryos. | overexpression | 5.25 | mesendoderm | blastoderm | 2 | Thierry Lepage | Development | 2006 | 133 | 2189 |
| Expression | bmp7 | negative | ndr1 | Ved expression is down-regulated at late blastula stage in snh/bmp7 mutants. | overexpression | 8 | margin | margin | 2 | Hammerschmidt, M. | Curr Biol | 2007 | 17 | 475 |
| Expression | calr | neutral | ndr2 | During gastrulation, calr eticulin transcripts are found in the dorsal mesendoderm, in the same cells that express the cyc gene. | 10660676:6 | 2 | 2 | Public | unknown | |||||
| Expression | ctnnb1 | positive | ndr1 | Injection of b-catenin RNA elicited the ectopic expression of boz/dharma at the sphere and shield stages | overexpression | 4.66 | margin | margin | 2 | Hirano, T. | Mechanisms of Development | 2000 | 91 | 293 |
| Expression | ctnnb1 | positive | ndr1 | At the onset of zygotic transcription, eta-catenin activates expression of nodal -related genes together with the homeobox genes bozozok / dharma / nieuwkoid ( bozozok ) in zebrafish, and siamois , twin in Xenopus ; these genes cooperatively promote organ | 11124801:10016 | 2 | 3 | Public | positive | |||||
| Expression | ctnnb1 | positive | ndr2 | Overexpression of ?-catenin induces cyc expression at 6 h (A), but not at 4 h (E, sphere) or 5 h (C, 40% epiboly). (G-J) Analysis of gsc expression at 5 hours in embryos from a ndr1 +/- intercross injected with ?-catenin or lacZ mRNA. ?-catenin mRNA (G), | 2 | 3 | Public | positive | ||||||
| Expression | ctnnb1 | positive | ndr2 | At the onset of zygotic transcription, eta-catenin activates expression of nodal -related genes together with the homeobox genes bozozok / dharma / nieuwkoid ( bozozok ) in zebrafish, and siamois , twin in Xenopus ; these genes cooperatively promote organ | 11124801:10016 | 2 | 3 | Public | positive | |||||
| Regulation | eomesa | unknown | ndr1 | This intriguing possibility was investigated further by animal pole injections, which indicated that eomes could modulate the induction of gsc and flh by ndr1 . | 2 | 6 | Public | unknown | ||||||
| Expression | fgf17 | negative | acvr1b | activation of the FGF/ERK pathway disrupts endoderm formation in the embryo and antagonizes the ability of an activated form of Tar/Acvr1b to induce endoderm at the animal pole. | overexpression | 5.25 | mesendoderm | blastoderm | 2 | Thierry Lepage | Development | 2006 | 133 | 2189 |
| Expression | fgf24 | negative | acvr1b | Microinjection of fgf24 leads to inhibition of bmp2b, bmp4 and bmp7 expression at blastula stage. | overexpression | 5.25 | mesendoderm | blastoderm | 2 | Thierry Lepage | Development | 2006 | 133 | 2189 |
| Expression | fgf3 | negative | acvr1b | Microinjection of fgf3 leads to inhibition of bmp2b expression at blastula stage. | overexpression | 5.25 | mesendoderm | blastoderm | 2 | Thierry Lepage | Development | 2006 | 133 | 2189 |
| Expression | fgf8 | negative | acvr1b | The fgf8 overexpression (10 pg) induced chd at the shield stage. | overexpression | 5.25 | mesendoderm | blastoderm | 2 | Thierry Lepage | Development | 2006 | 133 | 2189 |
| Expression | foxh1 | positive | ndr1 | FoxH1 is believed to drive transcription of the zebrafish Nodal-related genes and their antagonists, the lefties. | 2 | 2 | Public | positive | ||||||
| Expression | foxh1 | positive | ndr2 | FoxH1 is believed to drive transcription of the zebrafish Nodal-related genes and their antagonists, the lefties. | 2 | 2 | Public | positive | ||||||
| Expression | hsp90a.1 | positive | ndr2 | By extension, perhaps variations in genetic background, cold treatment and loss of HSP90 function also affect ndr1 penetrance via reductions in cyc transcription. | 2 | 2 | Public | positive | ||||||
| Expression | lft2 | negative | ndr2 | The phenotypic effects induced by overexpression of Antivin or Lefty2 might be caused by blocking Nodal signaling and/or by blocking expression of cyc and ndr1 . | 2 | 1 | Public | negative | ||||||
| Expression | lft2 | negative | ndr2 | axial expression is reduced in the midline and abolished in endodermal precursors of injected embryos. | overexpression | 8 | mesoderm | mesoderm | 2 | H. Joseph Yost | Development | 1999 | 126 | 3253 |
| Regulation | mapk1 | negative | acvr1b | FGF/ERK activity antagonizes the ability of tar*/acvr1b to induce endoderm. | 2 | 8 | Public | negative | ||||||
| Expression | myod1 | positive | oep | Formation of eye muscles doesn't form in oep mutant embryos at 42 hpf as judged from expression of myoD. | mutant embryos | 42 | eye muscles | musculature | 1 | Wolfgang Driever | Development | 1997 | 124 | 327 |
| Expression | ndr1 | positive | ndr1 | Maternal Ndr1 and Ndr2 mutant has normal expression of hgg1, a marker for anterior dorsal mesoderm, detected by whole-mount in situ hybridization in 10-somite-stage embryos. | MASO | 0.5 | blastomere | blastomere | 3 | Sampath, K. | Nature | 2005 | 438 | 1030 |
| Expression | ndr1 | neutral | ndr1 | The loss of gfp and ndr1 from the YSL could be due to decreased expression of an inducer of nodal-related gene expression, or to increased expression of an inhibitor. | 2 | 3 | Public | unknown | ||||||
| Expression | ndr1 | positive | ndr1 | The loss of gfp and ndr1 from the YSL could be due to decreased expression of an inducer of nodal-related gene expression, or to increased expression of an inhibitor. | 2 | 3 | Public | positive | ||||||
| Expression | ndr1 | positive | ndr2 | Maternal Ndr1 and Ndr2 mutant has normal expression of hgg1, a marker for anterior dorsal mesoderm, detected by whole-mount in situ hybridization in 10-somite-stage embryos. | MASO | 0.5 | blastomere | blastomere | 3 | Sampath, K. | Nature | 2005 | 438 | 1030 |
| Expression | ndr1 | neutral | ndr2 | Therefore, Cyc and ndr1 function as redundant signals that modulate cyc and pitx2a transcription in the dorsal forebrain. | 2 | 2 | Public | unknown | ||||||
| Expression | ndr1 | neutral | ndr2 | The loss of gfp and ndr1 from the YSL could be due to decreased expression of an inducer of nodal-related gene expression, or to increased expression of an inhibitor. | 2 | 3 | Public | unknown | ||||||
| Expression | ndr1 | positive | ndr2 | The loss of gfp and ndr1 from the YSL could be due to decreased expression of an inducer of nodal-related gene expression, or to increased expression of an inhibitor. | 2 | 3 | Public | positive | ||||||
| Expression | ndr1 | negative | bmp4 | 11291860 [PubMed - indexed for MEDLINE]Related ArticlesThe homeobox gene bozozok promotes anterior neuroectoderm formation in zebrafish through negative regulation of BMP2/4 and Wnt pathways. [Development. 2000] Cooperative roles of Bozozok/Dharma and Nod | 2 | 3 | Public | negative | ||||||
| Expression | ndr1 | positive | bon | overexpression of sqt elicited the ectopic expression of gsc and din in the entire blastoderm at the sphere to shield stage, but did not change the expression of boz/dharma. In the sqt mutant embryos, gsc expression was not detected, but din was expressed | mutant embryos | 5.25 | margin | margin | 1 | Derek L. Stemple | Current Biology | 1999 | 9 | 1147 |
| Expression | ndr1 | positive | chd | In sqt mutants, the bon expression domain is thinner along the animal/vegetal axis and exhibits a dorsal gap. Strikingly, cyc;sqt double mutants exhibit a barely detectable level of bon expression. | overexpression | 0 | DEL | blastoderm | 1, 2 | Hirano, T. | Mechanisms of Development | 2000 | 91 | 293 |
| Expression | ndr1 | neutral | dact1 | Thus, Boz, ndr1 , and Cyc are all capable of inducing dpr1 and dpr2 gene expression. | 2 | 1 | Public | unknown | ||||||
| Expression | ndr1 | positive | dact1 | Thus, Boz, ndr1 , and Cyc are all capable of inducing dpr1 and dpr2 gene expression. | 2 | 1 | Public | positive | ||||||
| Expression | ndr1 | positive | dact1 | The dorsalizing factors beta-catenin, Bozozok (Boz), Noggin (Nog), and the mesendoderm-inducing factor Squint (ndr1 ) are all able to induce ectopic expression of dpr1 and dpr2. | 15765513:5 | 2 | 3 | Public | positive | |||||
| Expression | ndr1 | positive | dkk1 | overexpression of sqt elicited the ectopic expression of gsc and din in the entire blastoderm at the sphere to shield stage, but did not change the expression of boz/dharma. In the sqt mutant embryos, gsc expression was not detected, but din was expressed | mutant embryos | 5.25 | mesendoderm | blastoderm | 1 | Didier Y. R. Stainier | Development | 2003 | 130 | 4989 |
| Expression | ndr1 | positive | fgf17 | overexpression of sqt elicited the ectopic expression of chd in the entire blastoderm at the sphere to shield stage. In the sqt mutant embryos din was expressed at reduced levels throughout the sphere and shield stages. | overexpression | 4 | YSL | YSL | 2 | Anming Meng | Developmental Biology | 2004 | 271 | 130 |
| Regulation | ndr1 | positive | flh | This intriguing possibility was investigated further by animal pole injections, which indicated that eomes could modulate the induction of gsc and flh by ndr1 . | 2 | 6 | Public | positive | ||||||
| Expression | ndr1 | positive | foxa2 | These results show that dorsal cyc expression is activated by sqt at 5 h, the first stage where a reduction of cyc expression is evident in sqt mutants. The reduction of cyc expression in sqt–/–; cyc+/– embryos when compared with sqt–/–; cyc+/+ mutants su | mutant embryos | 6 | mesendoderm | blastoderm | 1 | William S. Talbot | Development | 2003 | 130 | 1837 |
| Expression | ndr1 | positive | gsc | Thus overexpression of Ndr1/2 is sufficient to induce chd expression. But analysis of boz mutants and single and double mutants for the nodal-related genes shows that they are not essential for chd expression in the late blastula. | overexpression | 4 | YSL | YSL | 1, 2 | Hirano, T. | Mechanisms of Development | 2000 | 91 | 293 |
| Expression | ndr1 | positive | ndr1 | Maternal Ndr1 and Ndr2 mutant has normal expression of hgg1, a marker for anterior dorsal mesoderm, detected by whole-mount in situ hybridization in 10-somite-stage embryos. | MASO | 0.5 | blastomere | blastomere | 3 | Sampath, K. | Nature | 2005 | 438 | 1030 |
| Expression | ndr1 | neutral | ndr1 | The loss of gfp and ndr1 from the YSL could be due to decreased expression of an inducer of nodal-related gene expression, or to increased expression of an inhibitor. | 2 | 3 | Public | unknown | ||||||
| Expression | ndr1 | positive | ndr1 | The loss of gfp and ndr1 from the YSL could be due to decreased expression of an inducer of nodal-related gene expression, or to increased expression of an inhibitor. | 2 | 3 | Public | positive | ||||||
| Expression | ndr1 | positive | ndr2 | Maternal Ndr1 and Ndr2 mutant has normal expression of hgg1, a marker for anterior dorsal mesoderm, detected by whole-mount in situ hybridization in 10-somite-stage embryos. | MASO | 0.5 | blastomere | blastomere | 3 | Sampath, K. | Nature | 2005 | 438 | 1030 |
| Expression | ndr1 | neutral | ndr2 | Therefore, Cyc and ndr1 function as redundant signals that modulate cyc and pitx2a transcription in the dorsal forebrain. | 2 | 2 | Public | unknown | ||||||
| Expression | ndr1 | neutral | ndr2 | The loss of gfp and ndr1 from the YSL could be due to decreased expression of an inducer of nodal-related gene expression, or to increased expression of an inhibitor. | 2 | 3 | Public | unknown | ||||||
| Expression | ndr1 | positive | ndr2 | The loss of gfp and ndr1 from the YSL could be due to decreased expression of an inducer of nodal-related gene expression, or to increased expression of an inhibitor. | 2 | 3 | Public | positive | ||||||
| Expression | ndr1 | positive | ntl | overexpression of sqt elicited the ectopic expression of gsc and din in the entire blastoderm at the sphere to shield stage, but did not change the expression of boz/dharma. In the sqt mutant embryos, gsc expression was not detected, but din was expresse | overexpression | 5.25 | mesendoderm | blastoderm | 2 | Schier, A. F. | Development | 2003 | 130 | 5589 |
| Expression | ndr1 | positive | ntn1b | 10952887 [PubMed - indexed for MEDLINE]Related ArticlesA temperature-sensitive mutation in the nodal-related gene cyclops reveals that the floor plate is induced during gastrulation in zebrafish. [Development. 2003] Two distinct cell populations in the fl | 2 | 1 | Public | positive | ||||||
| Expression | ndr1 | positive | og9x | overexpression of sqt (ndr1) elicited the ectopic expression of gsc and din in the entire blastoderm at the sphere to shield stage, but did not change the expression of boz/dharma. In the sqt mutant embryos, gsc expression was not detected, but din was ex | mutant embryos | 5.25 | margin | margin | 1 | Thierry Lepage | Development | 2002 | 129 | 4901 |
| Expression | ndr1 | positive | otx2 | Injection with 1pg sqt or 10 pg of fgf17b mRNA caused ectopic expression of spr2. | mutant embryos | 10 | neuronectoderm | neuroectoderm | 1 | Didier Y. R. Stainier | Development | 2003 | 130 | 4989 |
| Expression | ndr1 | neutral | pitx2a | Therefore, Cyc and ndr1 function as redundant signals that modulate cyc and pitx2a transcription in the dorsal forebrain. | 2 | 2 | Public | unknown | ||||||
| Expression | ndr1 | positive | snai1a | overexpression of sqt elicited the ectopic expression of gsc and din in the entire blastoderm at the sphere to shield stage, but did not change the expression of boz/dharma. In the sqt mutant embryos, gsc expression was not detected, but din was expressed | overexpression | 5.25 | margin | margin | 2,4 | Anming Meng | The EMBO Journal | 2003 | 22 | 6078 |
| Expression | ndr1 | positive | sox17 | Almost all of the embryos injected with 0.5 pg sqt mRNA alone showed a large increase in ntl expression in the axial mesoderm. | mutant embryos | 6 | mesendoderm | blastoderm | 1 | William S. Talbot | Development | 2003 | 130 | 1837 |
| Expression | ndr1 | positive | sox32 | By contrast, in squint mutant embryos, the expression domain of og9x was thinner along the animalvegetal axis and displayed a gap. | overexpression | 6 | YSL | YSL | 2 | Hiroyuki Takeda | Mechanisms of Development | 2001 | 107 | 25 |
| Expression | ndr1 | positive | sp5l | overexpression of sqt elicited the ectopic expression of gsc and din in the entire blastoderm at the sphere to shield stage, but did not change the expression of boz/dharma. In the sqt mutant embryos, gsc expression was not detected, but din was expressed | overexpression | 5.25 | margin | margin | 2 | Anming Meng | The EMBO Journal | 2003 | 22 | 6078 |
| Expression | ndr2 | positive | ndr1 | The expression patterns of ndr1 and cyc are consistent with an elevated dorsal requirement for nodal-related gene function. | 2 | 6 | Public | positive | ||||||
| Expression | ndr2 | positive | ndr2 | The expression patterns of ndr1 and cyc are consistent with an elevated dorsal requirement for nodal-related gene function. | 2 | 6 | Public | positive | ||||||
| Expression | ndr2 | positive | ndr2 | Dorsal views at 50-60% epiboly. flh; gsc; twhh. Control embryos showing expression of all marker genes in the shield. overexpression of 0.05 pg of cyc+ RNA results in expansion of the flh domain, but not of gsc or twhh Injections of higher doses of cyc+ R | mutant embryos | 5.25 | margin | margin | 2 | Scott T. Dougan1 | Development | 2003 | 130 | 1837 |
| Expression | ndr2 | negative | bmp4 | 11291860 [PubMed - indexed for MEDLINE]Related ArticlesThe homeobox gene bozozok promotes anterior neuroectoderm formation in zebrafish through negative regulation of BMP2/4 and Wnt pathways. [Development. 2000] Cooperative roles of Bozozok/Dharma and Nod | 2 | 3 | Public | negative | ||||||
| Regulation | ndr2 | positive | chd | Cyc consistently induced mesodermal (Xbra, Xwnt8, actin), organizer (chordin) and neural (NCAM) markers. | 2 | 1 | Public | positive | ||||||
| Expression | ndr2 | neutral | dact1 | Thus, Boz, ndr1 , and Cyc are all capable of inducing dpr1 and dpr2 gene expression. | 2 | 1 | Public | unknown | ||||||
| Expression | ndr2 | positive | dact1 | Thus, Boz, ndr1 , and Cyc are all capable of inducing dpr1 and dpr2 gene expression. | 2 | 1 | Public | positive | ||||||
| Expression | ndr2 | positive | ehhadh | The nodal-related gene cyclops is not required for floor plate development in the absence of tbx1 6 gene function Previous work has shown that the nodal-related gene cyclops (cyc) is required for MFP formation (Hatta et al., 1991; Rebagliati et al., 1998 | 2 | 1 | Public | positive | ||||||
| Expression | ndr2 | negative | emx1 | Sirotkin and others Fig . 9. cyc represses anterior neural fates. (A-H) Expression of emx1 (most anterior label) and kr ox20 (R3 and R5 label) in embryos at the 2-somite stage (10.7 h). | 2 | 7 | Public | negative | ||||||
| Expression | ndr2 | positive | flh | Control embryos showing expression of all marker genes in the shield. overexpression of 0.05 pg of cyc+ RNA results in expansion of the flh domain, but not of gsc or twhh. Injections of higher doses of cyc+ RNA result in expansion of the gsc and twhh doma | overexpression | 5.25 | margin | margin | 2 | Schier, A. F. | Development | 2000 | 127 | 921 |
| Expression | ndr2 | positive | foxa2 | In 5 somite cyc -/ -embryos, zp-50 is expressed in rhombomeres r3 and r5 and the transverse domain in the posterior diencephalon. Arrowheads indicate missing zp-50 expression in the ventroanterior brain. | mutant embryos | 11.66 | ventral neural tube | neuroectoderm | 1 | P.W. Ingham | GENES & DEVELOPMENT | 1993 | 7 | 1436 |
| Expression | ndr2 | positive | gsc | Overexpression of Antivin and Lefty2 inhibits the expression of the dorsal markers goosecoid and sonic hedgehog ([36]; Figure 5J and Figure 5P; data not shown) whereas overexpression of ndr1 or Cyc induces ectopic goosecoid and hedgehog expression ([38, | 2 | 1 | Public | positive | ||||||
| Expression | ndr2 | positive | gsc | Overexpression of cyclops and squint at different doses leads to the induction of floating head at low doses and the induction of both goosecoid (Gsc) and floating head (Flh) at higher doses | overexpression | 5.25 | mesendoderm | blastoderm | 2 | Schier, A. F. | Development | 2000 | 127 | 921 |
| Expression | ndr2 | positive | lft1 | cyc mutant embryos do not express lft1 or lft2 in the anterior midline. | mutant embryos |