shani mutation in mouse affects splicing of Spata22 and leads to impaired meiotic recombination-Reference-Cited by-同舟云学术

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shani mutation in mouse affects splicing of Spata22 and leads to impaired meiotic recombination

Published:2020-05-10 Issue:2 Volume:129 Page:161-179
ISSN:0009-5915
Container-title:Chromosoma
language:en
Short-container-title:Chromosoma

Author:

Petrillo Cynthia,Barroca Vilma,Ribeiro Jonathan,Lailler Nathalie,Livera Gabriel,Keeney Scott^ORCID,Martini Emmanuelle,Jain Devanshi^ORCID

Funder

National Institutes of Health

Human Frontier Science Program

ANR

INSERM

Fondation ARC

La Ligue contre le Cancer

CEA

Howard Hughes Medical Institute

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

https://link.springer.com/content/pdf/10.1007/s00412-020-00735-8.pdf

Reference58 articles.

1. Barchi M, Mahadevaiah S, Di Giacomo M, Baudat F, de Rooij DG, Burgoyne PS, Jasin M, Keeney S (2005) Surveillance of different recombination defects in mouse spermatocytes yields distinct responses despite elimination at an identical developmental stage. Mol Cell Biol 25:7203–7215. https://doi.org/10.1128/MCB.25.16.7203-7215.2005

2. Baudat F, Manova K, Yuen JP, Jasin M, Keeney S (2000) Chromosome synapsis defects and sexually dimorphic meiotic progression in mice lacking Spo11. Mol Cell 6:989–998

3. Baudat F, Imai Y, de Massy B (2013) Meiotic recombination in mammals: localization and regulation. Nat Rev Genet 14:794–806. https://doi.org/10.1038/nrg3573

4. Bellve AR, Cavicchia JC, Millette CF, O'Brien DA, Bhatnagar YM, Dym M (1977) Spermatogenic cells of the prepuberal mouse. Isolation and morphological characterization. J Cell Biol 74:68–85

5. Blencowe BJ (2000) Exonic splicing enhancers: mechanism of action, diversity and role in human genetic diseases. Trends Biochem Sci 25:106–110. https://doi.org/10.1016/s0968-0004(00)01549-8

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1. Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia;Cell Cycle;2023-02-05

2. Bi‐allelic SPATA22 variants cause premature ovarian insufficiency and nonobstructive azoospermia due to meiotic arrest;Clinical Genetics;2022-03-16

3. Pathogenic variants in the human m6A reader YTHDC2 are associated with primary ovarian insufficiency;JCI Insight;2022-03-08

4. yama, a mutant allele of Mov10l1, disrupts retrotransposon silencing and piRNA biogenesis;PLOS Genetics;2021-02-26

5. yama, a mutant allele of Mov10l1, disrupts retrotransposon silencing and piRNA biogenesis;2020-11-26

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