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Ablation of Cypher, a PDZ-LIM domain Z-line protein, causes a severe form of congenital myopathy

  • Qiang Zhou
  • , Po Hsien Chu
  • , Chenqun Huang
  • , Ching Feng Cheng
  • , Maryann E. Martone
  • , Gudrun Knoll
  • , G. Diane Shelton
  • , Sylvia Evans
  • , Ju Chen*
  • *Corresponding author for this work
  • University of California at San Diego

Research output: Contribution to journalJournal Article peer-review

255 Scopus citations

Abstract

Cypher is a member of a recently emerging family of proteins containing a PDZ domain at their NH2 terminus and one or three LIM domains at their COOH terminus. Cypher knockout mice display a severe form of congenital myopathy and die postnatally from functional failure in multiple striated muscles. Examination of striated muscle from the mutants revealed that Cypher is not required for sarcomerogenesis or Z-line assembly, but rather is required for maintenance of the Z-line during muscle function. In vitro studies demonstrated that individual domains within Cypher localize independently to the Z-line via interactions with α-actinin or other Z-line components. These results suggest that Cypher functions as a linker-strut to maintain cytoskeletal structure during contraction.

Original languageEnglish
Pages (from-to)605-612
Number of pages8
JournalJournal of Cell Biology
Volume155
Issue number3
DOIs
StatePublished - 29 10 2001
Externally publishedYes

Keywords

  • Congenital myopathy
  • Cypher
  • LIM
  • PDZ
  • Z-line

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