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ZFIN ID: ZDB-PUB-010522-4
Ran binding protein RanBP1 in zebrafish embryonic development
Mangos, S., Vanderbeld, B., Krawetz, R., Sudol, K., and Kelly, G.M.
Date: 2001
Source: Molecular reproduction and development   59(3): 235-48 (Journal)
Registered Authors: Kelly, Greg, Krawetz, Roman, Mangos, Steve, Vanderbeld, Barb
Keywords: ran; RanBP1; zebrafish; embryogenesis; RNA interference
MeSH Terms:
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cloning, Molecular*
  • Humans
  • In Situ Hybridization
  • Microinjections
  • Molecular Sequence Data
  • Nuclear Proteins/chemistry
  • Nuclear Proteins/genetics
  • Nuclear Proteins/metabolism*
  • Phenotype
  • Precipitin Tests
  • RNA, Messenger/metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Xenopus laevis/metabolism
  • Zebrafish/embryology*
  • ran GTP-Binding Protein/chemistry
  • ran GTP-Binding Protein/genetics
  • ran GTP-Binding Protein/metabolism*
PubMed: 11424209 Full text @ Mol. Reprod. Dev.
Ran, which functions in nucleocytoplasmic transport and mitosis, binds to and is regulated in part by RanBP1. We have identified a zebrafish RanBP1 cDNA and report that it encodes for a polypeptide of 233 amino acids with considerable similarity to human and Xenopus RanBP1, despite the fact that it is 10% longer due to an extension at its carboxy terminus. RanBP1 mRNA is present as a maternal transcript and is expressed ubiquitously throughout the developing embryo. At the protein level, RanBP1 is present at all embryonic stages. Surprisingly, the ectopic overexpression of the protein had no obvious effect on embryogenesis. Attempts were also made to down-regulate RanBP1 activity by RNA interference. Injecting double-stranded RNA augmented both the mortality rate and the frequency of induced defects. Specific defects accompanied by changes in RanBP1 expression were not seen, leading us to propose that RNAi is not a reliable method for deregulating the activity of constitutively expressed genes, like RanBP1, in zebrafish.