نتایج جستجو برای: spo11 gene

تعداد نتایج: 1141470  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
James A Birchler Zhi Gao Fangpu Han

M eiosis takes the genetic variation from the parents and scrambles it before passing it on to the progeny. This partitioning is accomplished by two phenomena. First, because the genome is fractionated into chromosomes, the random segregation of nonhomologues transmits different parental contributions to the meiotic end products. Second, crossing over between homologous pairs of chromosomes cre...

2013
Doris Y. Lui Cori K. Cahoon Sean M. Burgess

Homolog pairing and crossing over during meiosis I prophase is required for accurate chromosome segregation to form euploid gametes. The repair of Spo11-induced double-strand breaks (DSB) using a homologous chromosome template is a major driver of pairing in many species, including fungi, plants, and mammals. Inappropriate pairing and crossing over at ectopic loci can lead to chromosome rearran...

2009
Sarah Zanders Eric Alani

Pch2 is a widely conserved protein that is required in baker's yeast for the organization of meiotic chromosome axes into specific domains. We provide four lines of evidence suggesting that it regulates the formation and distribution of crossover events required to promote chromosome segregation at Meiosis I. First, pch2Delta mutants display wild-type crossover levels on a small (III) chromosom...

2010
Rajeev Kumar Bernard de Massy

Meiotic recombination is initiated by the induction of programmed DNA double strand breaks (DSBs). DSB repair promotes homologous interactions and pairing and leads to the formation of crossovers (COs), which are required for the proper reductional segregation at the first meiotic division. In mammals, several hundred DSBs are generated at the beginning of meiotic prophase by the catalytic acti...

Journal: :Cold Spring Harbor perspectives in biology 2015
Lóránt Székvölgyi Kunihiro Ohta Alain Nicolas

Meiotic recombination is initiated by the formation of DNA double-strand breaks (DSBs) catalyzed by the evolutionary conserved Spo11 protein and accessory factors. DSBs are nonrandomly distributed along the chromosomes displaying a significant (~400-fold) variation of frequencies, which ultimately establishes local and long-range "hot" and "cold" domains for recombination initiation. This remar...

2015
Fabio Puddu Tobias Oelschlaegel Ilaria Guerini Nicola J Geisler Hengyao Niu Mareike Herzog Israel Salguero Bernardo Ochoa-Montaño Emmanuelle Viré Patrick Sung David J Adams Thomas M Keane Stephen P Jackson

DNA double-strand break (DSB) repair by homologous recombination (HR) requires 3' single-stranded DNA (ssDNA) generation by 5' DNA-end resection. During meiosis, yeast Sae2 cooperates with the nuclease Mre11 to remove covalently bound Spo11 from DSB termini, allowing resection and HR to ensue. Mitotic roles of Sae2 and Mre11 nuclease have remained enigmatic, however, since cells lacking these d...

Journal: :Genetics 2009
Siim Pauklin Julia S Burkert Julie Martin Fekret Osman Sandra Weller Simon J Boulton Matthew C Whitby Svend K Petersen-Mahrt

Meiotic recombination enhances genetic diversity as well as ensures proper segregation of homologous chromosomes, requiring Spo11-initiated double-strand breaks (DSBs). DNA deaminases act on regions of single-stranded DNA and deaminate cytosine to uracil (dU). In the immunoglobulin locus, this lesion will initiate point mutations, gene conversion, and DNA recombination. To begin to delineate th...

Journal: :Genetics 2013
Milorad Kojic Jeanette H Sutherland José Pérez-Martín William K Holloman

A central feature of meiosis is the pairing and recombination of homologous chromosomes. Ustilago maydis, a biotrophic fungus that parasitizes maize, has long been utilized as an experimental system for studying recombination, but it has not been clear when in the life cycle meiotic recombination initiates. U. maydis forms dormant diploid teliospores as the end product of the infection process....

Journal: :Genetics 1993
M Ajimura S H Leem H Ogawa

Mutants defective in meiotic recombination were isolated from a disomic haploid strain of Saccharomyces cerevisiae by examining recombination within the leu2 and his4 heteroalleles located on chromosome III. The mutants were classified into two new complementation groups (MRE2 and MRE11) and eight previously identified groups, which include SPO11, HOP1, REC114, MRE4/MEK1 and genes in the RAD52 ...

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