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  Mutations that affect meiosis in male mice influence the dynamics of the mid-preleptotene and bouquet stages

Liebe, B., Petukhova, G., Barchi, M., Bellani, M., Braselmann, H., Nakano, T., et al. (2006). Mutations that affect meiosis in male mice influence the dynamics of the mid-preleptotene and bouquet stages. Experimental Cell Research, 312(19), 3768-3781. doi:10.1016/j.yexcr.2006.07.019.

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Genre: Zeitschriftenartikel
Alternativer Titel : Exp. Cell Res.

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 Urheber:
Liebe, Bodo1, Autor
Petukhova, G., Autor
Barchi, M., Autor
Bellani, M., Autor
Braselmann, H., Autor
Nakano, T., Autor
Pandita, T. K., Autor
Jasin, M., Autor
Fornace, A., Autor
Meistrich, M. L., Autor
Baarends, W. M., Autor
Schimenti, J., Autor
de Lange, T., Autor
Keeney, S., Autor
Camerini-Otero, R. D., Autor
Scherthan, Harry2, Autor           
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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Schlagwörter: ATM; previous termBouquetnext term; DSB; previous termMeiosis; Mousenext term; Recombination; Telomere; Spermatogenesis
 Zusammenfassung: previous termMeiosisnext term pairs and segregates homologous chromosomes and thereby forms haploid germ cells to compensate the genome doubling at fertilization. Homologue pairing in many eukaryotic species depends on formation of DNA double strand breaks (DSBs) during early prophase I when telomeres begin to cluster at the nuclear periphery (previous termbouquet stage)next term. By fluorescence in situ hybridization criteria, we observe that previous termmid-preleptotene and bouquet stagenext term frequencies are altered in previous termmale micenext term deficient for proteins required for recombination, ubiquitin conjugation and telomere length control. The generally low frequencies of previous termmid-preleptotenenext term spermatocytes were significantly increased in previous termmale micenext term lacking recombination proteins SPO11, MEI1, MLH1, KU80, ubiquitin conjugating enzyme HR6B, and in previous termmicenext term with only one copy of the telomere length regulator Terf1. The previous termbouquet stagenext term was significantly enriched in Atm−/−, Spo11−/−, Mei1m1Jcs/m1Jcs, Mlh1−/−, Terf1+/− and Hr6b−/− spermatogenesis, but not in previous termmicenext term lacking recombination proteins DMC1 and HOP2, the non-homologous end-joining DNA repair factor KU80 and the ATM downstream effector GADD45a. previous termMicenext term defective in spermiogenesis (Tnp1−/−, Gmcl1−/−, Asm−/−) showed wild-type previous termmid-preleptotene and bouquetnext term frequencies. A low frequency of previous termbouquetnext term spermatocytes in Spo11−/−Atm−/− spermatogenesis suggests that DSBs contribute to the Atm−/−-correlated previous termbouquet stagenext term exit defect. Insignificant changes of previous termbouquetnext term frequencies in previous termmicenext term with defects in early previous termstagesnext term of DSB repair (Dmc1−/−, Hop2−/−) suggest that there is an ATM-specific previous terminfluence on bouquet stagenext term duration. Altogether, it appears that several pathways previous terminfluencenext term telomere previous termdynamicsnext term in mammalian previous termmeiosis.next term

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Sprache(n): eng - English
 Datum: 2006-11-15
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: eDoc: 307712
DOI: 10.1016/j.yexcr.2006.07.019
 Art des Abschluß: -

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Titel: Experimental Cell Research
  Alternativer Titel : Exp. Cell Res.
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 312 (19) Artikelnummer: - Start- / Endseite: 3768 - 3781 Identifikator: ISSN: 0014-4827