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The Meiotic Nuclear Lamina Regulates Chromosome Dynamics and Promotes Efficient Homologous Recombination in the Mouse

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-96285
  • The nuclear lamina is the structural scaffold of the nuclear envelope and is well known for its central role in nuclear organization and maintaining nuclear stability and shape. In the past, a number of severe human disorders have been identified to be associated with mutations in lamins. Extensive research on this topic has provided novel important clues about nuclear lamina function. These studies have contributed to the knowledge that the lamina constitutes a complex multifunctional platform combining both structural and regulatoryThe nuclear lamina is the structural scaffold of the nuclear envelope and is well known for its central role in nuclear organization and maintaining nuclear stability and shape. In the past, a number of severe human disorders have been identified to be associated with mutations in lamins. Extensive research on this topic has provided novel important clues about nuclear lamina function. These studies have contributed to the knowledge that the lamina constitutes a complex multifunctional platform combining both structural and regulatory functions. Here, we report that, in addition to the previously demonstrated significance for somatic cell differentiation and maintenance, the nuclear lamina is also an essential determinant for germ cell development. Both male and female mice lacking the short meiosis-specific A-type lamin C2 have a severely defective meiosis, which at least in the male results in infertility. Detailed analysis revealed that lamin C2 is required for telomere-driven dynamic repositioning of meiotic chromosomes. Loss of lamin C2 affects precise synapsis of the homologs and interferes with meiotic double-strand break repair. Taken together, our data explain how the nuclear lamina contributes to meiotic chromosome behaviour and accurate genome haploidization on a mechanistic level.zeige mehrzeige weniger

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Autor(en): Manfred Alsheimer, Jana Link, Daniel Jahn, Johannes Schmitt, Eva Göb, Johannes Baar, Sagrario Ortega, Ricardo Benavente
URN:urn:nbn:de:bvb:20-opus-96285
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Fakultät für Biologie / Theodor-Boveri-Institut für Biowissenschaften
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):PLoS Genetics
Erscheinungsjahr:2013
Originalveröffentlichung / Quelle:In: PLoS Genetics (2013) 9: 1, doi:10.1371/journal.pgen.1003261
DOI:https://doi.org/10.1371/journal.pgen.1003261
Allgemeine fachliche Zuordnung (DDC-Klassifikation):5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Freie Schlagwort(e):Oocytes; homologous chromosomes; homologous recombination; lamins; spermatocytes; synapsis; telomeres; testes
Datum der Freischaltung:28.04.2014
Sammlungen:Open-Access-Publikationsfonds / Förderzeitraum 2013
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung