protein
| interacting with NEUROD1 (could activate insulin gene transcription synergistically) |
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transcriptional activator for insulin gene expression, and the interactions of ISL1 with NEUROD1 are required for the transcriptional activity of the insulin gene |
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FBXO25 acts as an ubiquitin E3 ligase to target cardiac transcription factors including NKX2-5, ISL1, and HAND1, indicating that cardiac protein homeostasis through FBXO25 has a pivotal impact on cardiac development |
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binds to a known POU4F1-regulated enhancer in the NEUROD4 gene, suggesting a mechanism of interaction between these genes |
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novel transcriptional regulator of LHX3 |
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ISL1 directly regulates FGF10 transcription during human cardiac outflow formation |
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AJUBA binds ISL1, represses its transcriptional activity, and is also required for autorepression of ISL1 expression in an Retinoic acid (RA)-dependent manner |
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LDB1 is a critical transcriptional coregulator during islet alpha-, beta-, and delta-cell development through ISL1-dependent and potentially ISL1-independent control |
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CDH6 is necessary for the generation of ISL1-positive dorsal interneurons, as well as the initiation of pre-migratory neural crest cell emigration |
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potent BARX1 functions in intestinal rotation and stomach myogenesis occur through ISL1, PITX1, SIX2 and PITX2, intermediary transcription factors |
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LDB1 binds to the key regulator of cardiac progenitors, ISL1, and protects it from degradation |
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is a transcription factor important for pancreatic islet cell development, maturation, and function, which largely requires interaction with LDB1 coregulator |
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SSBP3 interacts with LDB1 and ISL1 in beta-cell lines and in human islets and is coexpressed with LDB1 and ISL1 pancreas tissue |
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SSBP3 is a critical component of LDB1-ISL1 regulatory complexes, required for expression of critical beta-cell target genes |
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NRDC controls beta-cell function via regulation of the ISL1-MAFA pathway |
| Mice with a homozygous null mutation in the Isl1 gene exhibited growth retardation and heart abnormalities (Cai et al, 2003) | |
Mouse conditional knockout for Isl1 gene showed a loss of the nociceptive markers TrkA, TrkB and Runx1 and a near absence of cutaneous innervation, an excess of cell apoptosis, a ganglion size markedly diminished, a profound loss of cutaneous innervation. Mouse Isl1 CKO exhibits rofound deficits in the sensory innervation of the CNS and periphery, extensive changes in sensory gene expression, and markedly increased sensory apoptosis, with relative sparing of proprioceptor neuron (Sun et al, 2008) |