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  CRIS - a novel cAMP-binding protein controlling spermiogenesis and the development of flagellar bending

Krähling, M., Alvarez, L., Debowski, K., Van, Q., Gunkel, M., Irsen, S., et al. (2013). CRIS - a novel cAMP-binding protein controlling spermiogenesis and the development of flagellar bending. PLoS Genetics, 9(12): e1003960. doi:10.1371/journal.pgen.1003960.

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 Creators:
Krähling, Miriam1, Author           
Alvarez, Luis1, Author           
Debowski, K., Author
Van, Q., Author
Gunkel, Monika1, Author           
Irsen, Stephan2, Author           
Al-Amoudi, A., Author
Strünker, Timo1, Author           
Kremmer, E., Author
Krause, E., Author
Voigt, I., Author
Wörtge, S., Author
Waisman, A., Author
Weyand, I., Author
Seifert, Reinhard1, Author           
Kaupp, Ulrich Benjamin1, Author           
Wachten, Dagmar1, Author           
Affiliations:
1Department of Molecular Sensory Systems, Center of Advanced European Studies and Research (caesar), Max Planck Society, ou_2173679              
2Electron Microscopy and Analytics, Center of Advanced European Studies and Research (caesar), Max Planck Society, ou_2173680              

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 Abstract: The second messengers cAMP and cGMP activate their target proteins by binding to a conserved cyclic nucleotide-binding domain (CNBD). Here, we identify and characterize an entirely novel CNBD-containing protein called CRIS (cyclic nucleotide receptor involved in sperm function) that is unrelated to any of the other members of this protein family. CRIS is exclusively expressed in sperm precursor cells. Cris-deficient male mice are either infertile due to a lack of sperm resulting from spermatogenic arrest, or subfertile due to impaired sperm motility. The motility defect is caused by altered Ca2+ regulation of flagellar beat asymmetry, leading to a beating pattern that is reminiscent of sperm hyperactivation. Our results suggest that CRIS interacts during spermiogenesis with Ca2+-regulated proteins that—in mature sperm—are involved in flagellar bending.

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Language(s): eng - English
 Dates: 2013
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1371/journal.pgen.1003960
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Title: PLoS Genetics
  Abbreviation : PLoS Genet
Source Genre: Journal
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Publ. Info: San Francisco, CA : Public Library of Science
Pages: - Volume / Issue: 9 (12) Sequence Number: e1003960 Start / End Page: - Identifier: ISSN: 1553-7390
CoNE: https://pure.mpg.de/cone/journals/resource/1000000000017180