<p>We propose that DSBs induced by SPO11 at the beginning of meiotic prophase are sensed by the MRE11 complex, which activates ATM. ATM inhibits further DSB formation via a feedback loop and promotes DSB repair. ATM activates CHK2, which controls cell cycle progression but is not involved in regulating DSB formation. Recombination progression leads to homologous chromosome synapsis and sex body formation. Besides participating in recombination, TRIP13 is also needed for effective sex body formation. Proper recombination and sex body formation are required to permit meiotic progression.</p
SummaryThe Mre11 complex (consisting of MRE11, RAD50, and NBS1/Xrs2) is required for double-strand b...
AbstractBackground: Checkpoint pathways prevent cell-cycle progression in the event of DNA lesions. ...
textabstractRepair of SPO11-dependent DNA double-strand breaks (DSBs) via homologous recombination (...
In many organisms, developmentally programmed double-strand breaks (DSBs) formed by the SPO11 transe...
Ataxia-telangiectasia mutated (ATM) and RAD3-related (ATR) are widely known as being central players...
ATM is a member of the phosphatidylinositol 3-kinase (PIK)like kinases, some of which are active in ...
During meiosis in most sexually reproducing organisms, recombination forms crossovers between homolo...
The ATM and ATR protein kinases play central roles in the cellular response to double-strand breaks ...
Meiotic recombination is initiated by SPO11-induced double-strand breaks (DSBs). In most mammals, th...
In most taxa, halving of chromosome numbers during meiosis requires that homologous chromosomes (hom...
Most mutations that compromise meiotic recombination or synapsis in mouse spermatocytes result in ar...
During meiosis, formation and repair of programmed DNA double-strand breaks (DSBs) create genetic ex...
<div><p>Most mutations that compromise meiotic recombination or synapsis in mouse spermatocytes resu...
During meiosis in most sexually reproducing organisms, recombination forms crossovers between homolo...
<div><p>An essential feature of meiosis is Spo11 catalysis of programmed DNA double strand breaks (D...
SummaryThe Mre11 complex (consisting of MRE11, RAD50, and NBS1/Xrs2) is required for double-strand b...
AbstractBackground: Checkpoint pathways prevent cell-cycle progression in the event of DNA lesions. ...
textabstractRepair of SPO11-dependent DNA double-strand breaks (DSBs) via homologous recombination (...
In many organisms, developmentally programmed double-strand breaks (DSBs) formed by the SPO11 transe...
Ataxia-telangiectasia mutated (ATM) and RAD3-related (ATR) are widely known as being central players...
ATM is a member of the phosphatidylinositol 3-kinase (PIK)like kinases, some of which are active in ...
During meiosis in most sexually reproducing organisms, recombination forms crossovers between homolo...
The ATM and ATR protein kinases play central roles in the cellular response to double-strand breaks ...
Meiotic recombination is initiated by SPO11-induced double-strand breaks (DSBs). In most mammals, th...
In most taxa, halving of chromosome numbers during meiosis requires that homologous chromosomes (hom...
Most mutations that compromise meiotic recombination or synapsis in mouse spermatocytes result in ar...
During meiosis, formation and repair of programmed DNA double-strand breaks (DSBs) create genetic ex...
<div><p>Most mutations that compromise meiotic recombination or synapsis in mouse spermatocytes resu...
During meiosis in most sexually reproducing organisms, recombination forms crossovers between homolo...
<div><p>An essential feature of meiosis is Spo11 catalysis of programmed DNA double strand breaks (D...
SummaryThe Mre11 complex (consisting of MRE11, RAD50, and NBS1/Xrs2) is required for double-strand b...
AbstractBackground: Checkpoint pathways prevent cell-cycle progression in the event of DNA lesions. ...
textabstractRepair of SPO11-dependent DNA double-strand breaks (DSBs) via homologous recombination (...