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  Cohesin SMC1b is required for meiotic chromosome dynamics, sister chromatid cohesion and DNA recombination

Revenkova, E., Eijpe, M., Heyting, C., Hodges, C. A., Hunt, P. A., Liebe, B., et al. (2004). Cohesin SMC1b is required for meiotic chromosome dynamics, sister chromatid cohesion and DNA recombination. Nature Cell Biology, 6(6), 555-562. doi:10.1038/ncb1135.

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Genre: Journal Article
Alternative Title : Nat Cell Biol

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 Creators:
Revenkova, Ekaterina, Author
Eijpe, Maureen, Author
Heyting, Christa, Author
Hodges, Craig A., Author
Hunt, Patricia A., Author
Liebe, Bodo1, Author
Scherthan, Harry2, Author           
Jessberger, Rolf, Author
Affiliations:
1Max Planck Society, ou_persistent13              
2Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433549              

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 Abstract: Sister chromatid cohesion ensures the faithful segregation of chromosomes in mitosis and in both meiotic divisions1, 2, 3, 4. Meiosis-specific components of the cohesin complex, including the recently described SMC1 isoform SMC1beta5, were suggested to be required for meiotic sister chromatid cohesion and DNA recombination. Here we show that SMC1beta-deficient mice of both sexes are sterile. Male meiosis is blocked in pachytene; female meiosis is highly error-prone but continues until metaphase II. Prophase axial elements (AEs) are markedly shortened, chromatin extends further from the AEs, chromosome synapsis is incomplete, and sister chromatid cohesion in chromosome arms and at centromeres is lost prematurely. In addition, crossover-associated recombination foci are absent or reduced, and meiosis-specific perinuclear telomere arrangements are impaired. Thus, SMC1beta has a key role in meiotic cohesion, the assembly of AEs, synapsis, recombination, and chromosome movements.

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Language(s): eng - English
 Dates: 2004-05-16
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: -
 Identifiers: eDoc: 225138
DOI: 10.1038/ncb1135
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Title: Nature Cell Biology
  Alternative Title : Nat Cell Biol
Source Genre: Journal
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Pages: - Volume / Issue: 6 (6) Sequence Number: - Start / End Page: 555 - 562 Identifier: ISSN: 1465-7392