ATM promotes the obligate XY crossover and both crossover control and chromosome axis integrity on autosomes - Wikidata - wikimedia - TriplyDB

ATM promotes the obligate XY crossover and both crossover control and chromosome axis integrity on autosomes

ATM promotes the obligate XY crossover and both crossover control and chromosome axis integrity on autosomes

http://www.wikidata.org/entity/Q21145047

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Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements Double-strand break repair on sex chromosomes: challenges during male meiotic prophase Variation in genome-wide levels of meiotic recombination is established at the onset of prophase in mammalian males Mammalian BTBD12 (SLX4) protects against genomic instability during mammalian spermatogenesis Spata22, a novel vertebrate-specific gene, is required for meiotic progress in mouse germ cells Mouse TRIP13/PCH2 is required for recombination and normal higher-order chromosome structure during meiosis ATM controls meiotic double-strand-break formation Pch2 links chromosome axis remodeling at future crossover sites and crossover distribution during yeast meiosis Modulating Crossover Frequency and Interference for Obligate Crossovers in Saccharomyces cerevisiae Meiosis.Genetic analysis of baker's yeast Msh4-Msh5 reveals a threshold crossover level for meiotic viability.Amplifying recombination genome-wide and reshaping crossover landscapes in Brassicas.Pseudosynapsis and decreased stringency of meiotic repair pathway choice on the hemizygous sex chromosome of Caenorhabditis elegans males Mouse HORMAD1 is a meiosis i checkpoint protein that modulates DNA double- strand break repair during female meiosis.Male fertility defect associated with disrupted BRCA1-PALB2 interaction in mice The expression profile of the major mouse SPO11 isoforms indicates that SPO11beta introduces double strand breaks and suggests that SPO11alpha has an additional role in prophase in both spermatocytes and oocytes.The meiotic checkpoint network: step-by-step through meiotic prophase Mouse tetrad analysis provides insights into recombination mechanisms and hotspot evolutionary dynamics.Reinterpretation of evidence advanced for neo-oogenesis in mammals, in terms of a finite oocyte reserve DNA double-strand break repair in Caenorhabditis elegans Meiotic cohesin SMC1β provides prophase I centromeric cohesion and is required for multiple synapsis-associated functions.Sam68 marks the transcriptionally active stages of spermatogenesis and modulates alternative splicing in male germ cells.Distinct properties of the XY pseudoautosomal region crucial for male meiosis.The ATM signaling cascade promotes recombination-dependent pachytene arrest in mouse spermatocytes.Genetic evidence that synaptonemal complex axial elements govern recombination pathway choice in mice Mammalian recombination hot spots: properties, control and evolution.Drosophila ATM and ATR have distinct activities in the regulation of meiotic DNA damage and repair Meiotic functions of RAD18.Meiotic double-strand breaks occur once per pair of (sister) chromatids and, via Mec1/ATR and Tel1/ATM, once per quartet of chromatids Reduced Crossover Interference and Increased ZMM-Independent Recombination in the Absence of Tel1/ATM.Homeostatic control of recombination is implemented progressively in mouse meiosis.Targeted inactivation of nuclear interaction partner of ALK disrupts meiotic prophase.Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice.The ATM signaling network in development and disease.Double-strand break repair by homologous recombination in primary mouse somatic cells requires BRCA1 but not the ATM kinase The tricky path to recombining X and Y chromosomes in meiosis.A surge of late-occurring meiotic double-strand breaks rescues synapsis abnormalities in spermatocytes of mice with hypomorphic expression of SPO11.Numerical constraints and feedback control of double-strand breaks in mouse meiosis Control of Meiotic Crossovers: From Double-Strand Break Formation to Designation.Initiation of meiotic recombination in mammals.Dynamics of DOT1L localization and H3K79 methylation during meiotic prophase I in mouse spermatocytes.

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ATM promotes the obligate XY crossover and both crossover control and chromosome axis integrity on autosomes

http://www.wikidata.org/entity/Q21145047

description

2008 nî lūn-bûn

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2008 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2008 թվականի մայիսին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

ATM promotes the obligate XY c ...... me axis integrity on autosomes

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ATM promotes the obligate XY c ...... me axis integrity on autosomes

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ATM promotes the obligate XY c ...... me axis integrity on autosomes

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ATM promotes the obligate XY c ...... me axis integrity on autosomes

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type

label

ATM promotes the obligate XY c ...... me axis integrity on autosomes

@ast

ATM promotes the obligate XY c ...... me axis integrity on autosomes

@en

ATM promotes the obligate XY c ...... me axis integrity on autosomes

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ATM promotes the obligate XY c ...... me axis integrity on autosomes

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ATM Promotes the Obligate XY C ...... me Axis Integrity on Autosomes

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prefLabel

ATM promotes the obligate XY c ...... me axis integrity on autosomes

@ast

ATM promotes the obligate XY c ...... me axis integrity on autosomes

@en

ATM promotes the obligate XY c ...... me axis integrity on autosomes

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ATM promotes the obligate XY c ...... me axis integrity on autosomes

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JOURNAL.PGEN.1000076

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P1476

ATM promotes the obligate XY c ...... me axis integrity on autosomes

@en

P2860

Surveillance of different recombination defects in mouse spermatocytes yields distinct responses despite elimination at an identical developmental stage.

Distinct DNA-damage-dependent and -independent responses drive the loss of oocytes in recombination-defective mouse mutants

A pathway of double-strand break rejoining dependent upon ATM, Artemis, and proteins locating to gamma-H2AX foci.

Physical and functional interactions among basic chromosome organizational features govern early steps of meiotic chiasma formation.

Crossover assurance and crossover interference are distinctly regulated by the ZMM proteins during yeast meiosis.

Saccharomyces cerevisiae checkpoint genes MEC1, RAD17 and RAD24 are required for normal meiotic recombination partner choice

Crossover/noncrossover differentiation, synaptonemal complex formation, and regulatory surveillance at the leptotene/zygotene transition of meiosis.

The time course and chromosomal localization of recombination-related proteins at meiosis in the mouse are compatible with models that can resolve the early DNA-DNA interactions without reciprocal recombination

Meiotic crossing-over: obligation and interference

Shelterin: the protein complex that shapes and safeguards human telomeres

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e1000076

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scholarly article

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10.1371/JOURNAL.PGEN.1000076

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5

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4

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Monica Di Giacomo

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2008-05-01T00:00:00Z

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5351994

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18497861

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2374915

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