PUBLICATION

Structure and characterization of the murine p80 coilin gene, Coil

Authors
Tucker, K.E., Massello, L.K., Gao, L., Barber, T.J., Hebert, M.D., Chan, E.K., and Matera, A.G.
ID
ZDB-PUB-030806-3
Date
2000
Source
Journal of structural biology   129(2-3): 269-277 (Journal)
Registered Authors
Keywords
none
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Brain/metabolism
  • Chromosome Mapping*
  • Cloning, Molecular
  • Coiled Bodies/genetics
  • Coiled Bodies/ultrastructure
  • Exons
  • Genomic Library
  • Humans
  • Mice
  • Molecular Sequence Data
  • Nuclear Proteins/chemistry
  • Nuclear Proteins/genetics*
  • Phosphoproteins/genetics
  • Ranidae
  • Recombinant Proteins/biosynthesis
  • Recombinant Proteins/chemistry
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Sequence Homology, Nucleic Acid
PubMed
10806077 Full text @ J. Struct. Biol.
Abstract
Cajal bodies (coiled bodies, CBs) are nuclear organelles of unknown function and are characterized by a wide variety of components including various basal transcription and cell cycle proteins, the nucleolar proteins fibrillarin and Nopp140, numerous small nuclear ribonucleoproteins, the survival motor neuron protein complex, and the marker protein, p80 coilin. To gain insight into the role of p80 coilin in CBs, we have cloned the murine gene Coil and have mapped it to the distal portion of chromosome band 11D. The approximately 2.6-kb transcript is detectable in all tissues analyzed, with the highest levels in brain and testis. Sequence analysis shows that, like its human counterpart, the mouse coilin gene is composed of seven exons and spans nearly 30 kb of genomic DNA. The predicted amino acid sequence reveals two conserved N- and C-terminal domains, and comparison with the Xenopus SPH-1 protein reveals that these three genes are indeed orthologous. These results should facilitate gene disruption experiments aimed at creating a genetic model system to study CBs.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping