ZFIN ID: ZDB-PUB-200611-4
Loss of the RNA-binding protein Rbm15 disrupts liver maturation in zebrafish
Hu, L., Li, H., Chi, Z., He, J.
Date: 2020
Source: The Journal of biological chemistry   295(33): 11466-11472 (Journal)
Registered Authors: He, Jianbo, Li, Hongyan
Keywords: RNA binding motif protein 15 (Rbm15), RNA binding protein, gene regulation, hepatocyte nuclear factor 4 (HNF-4), liver maturation, liver organogenesis, mTORC1, post-transcriptional regulation, zebrafish
MeSH Terms:
  • Animals
  • Apoptosis
  • CRISPR-Cas Systems
  • Cell Differentiation
  • Cell Proliferation
  • Gene Deletion*
  • Gene Expression Regulation, Developmental*
  • Hepatocytes/cytology
  • Hepatocytes/metabolism
  • Liver/cytology
  • Liver/embryology*
  • Zebrafish/embryology*
  • Zebrafish/genetics
PubMed: 32518161 Full text @ J. Biol. Chem.
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ABSTRACT
Liver organogenesis begins with hepatic precursors in the foregut endoderm, followed by hepatoblast specification, differentiation, outgrowth, and maturation for the formation of functional hepatocytes. Although several signaling pathways and critical factors that regulate liver specification, differentiation, and proliferation have been identified, little is known about how liver maturation is regulated. Here, we used a screen for mutations affecting liver development in zebrafish and identified a cq96 mutant that exhibits a specific defect in liver maturation. Results from positional cloning revealed that cq96 encodes an RNA-binding protein, Rbm15, which is an evolutionarily conserved Spen family protein and known to play a crucial role in RNA m6A modification, nuclear export, and alternative splicing. However, a function of Rbm15 in embryonic liver development has not been reported. We found that Rbm15 is specifically expressed in the liver after its differentiation. CRISPR/Cas9-mediated loss of rbm15 repressed hepatic maturation, but did not affect hepatoblast specification, differentiation, and hepatocyte proliferation and apoptosis. Additional experiments disclosed that the mTOR complex 1 (mTORC1) pathway is highly activated in rbm15-deficient hepatocytes. Moreover, rapamycin treatment partially restored normal hepatic gene expression as well as the nuclear location of the transcription factor Hnf4a. Taken together, these results reveal an unexpected role of Rbm15 in liver maturation.
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