Cargando…

Complex Breakpoints and Template Switching Associated with Non-canonical Termination of Homologous Recombination in Mammalian Cells

A proportion of homologous recombination (HR) events in mammalian cells resolve by “long tract” gene conversion, reflecting copying of several kilobases from the donor sister chromatid prior to termination. Cells lacking the major hereditary breast/ovarian cancer predisposition genes, BRCA1 or BRCA2...

Descripción completa

Detalles Bibliográficos
Autores principales:	Hartlerode, Andrea J., Willis, Nicholas A., Rajendran, Anbazhagan, Manis, John P., Scully, Ralph
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2016
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5104497/ https://www.ncbi.nlm.nih.gov/pubmed/27832076 http://dx.doi.org/10.1371/journal.pgen.1006410

Ejemplares similares

Correction: Complex Breakpoints and Template Switching Associated with Non-canonical Termination of Homologous Recombination in Mammalian Cells
por: Hartlerode, Andrea J., et al.
Publicado: (2016)

Cell Cycle-Dependent Induction of Homologous Recombination by a Tightly Regulated I-SceI Fusion Protein
por: Hartlerode, Andrea, et al.
Publicado: (2011)

Rad51 recruitment and exclusion of non-homologous end joining during homologous recombination at a Tus/Ter mammalian replication fork barrier
por: Willis, Nicholas A., et al.
Publicado: (2018)

BRCA1 controls homologous recombination at Tus/Ter-stalled mammalian replication forks
por: Willis, Nicholas A., et al.
Publicado: (2014)

Impact of Histone H4 Lysine 20 Methylation on 53BP1 Responses to Chromosomal Double Strand Breaks
por: Hartlerode, Andrea J., et al.
Publicado: (2012)

PARP3 affects the relative contribution of homologous recombination and nonhomologous end-joining pathways
por: Beck, Carole, et al.
Publicado: (2014)

Role of mammalian Mre11 in classical and alternative non-homologous end joining
por: Xie, Anyong, et al.
Publicado: (2009)

Precise detection of rearrangement breakpoints in mammalian chromosomes
por: Lemaitre, Claire, et al.
Publicado: (2008)

Repair of gaps opposite lesions by homologous recombination in mammalian cells
por: Adar, Sheera, et al.
Publicado: (2009)

Visualization of recombination–mediated damage-bypass by template switching
por: Giannattasio, Michele, et al.
Publicado: (2014)

Identifying the Important HIV-1 Recombination Breakpoints
por: Archer, John, et al.
Publicado: (2008)

Fixing DNA breaks during class switch recombination
por: Jolly, Christopher J., et al.
Publicado: (2008)

SPIDR is required for homologous recombination during mammalian meiosis
por: Huang, Tao, et al.
Publicado: (2023)

DEK is required for homologous recombination repair of DNA breaks
por: Smith, Eric A., et al.
Publicado: (2017)

Switch recombination breakpoints are strictly correlated with DNA recognition motifs for immunoglobulin S gamma 3 DNA-binding proteins
Publicado: (1992)

Interplay between Synaptonemal Complex, Homologous Recombination, and Centromeres during Mammalian Meiosis
por: Qiao, Huanyu, et al.
Publicado: (2012)

Replication and Recombination Factors Contributing to Recombination-Dependent Bypass of DNA Lesions by Template Switch
por: Vanoli, Fabio, et al.
Publicado: (2010)

Accurate Detection of Recombinant Breakpoints in Whole-Genome Alignments
por: Westesson, Oscar, et al.
Publicado: (2009)

The dual role of HOP2 in mammalian meiotic homologous recombination
por: Pezza, Roberto J., et al.
Publicado: (2014)

Reappearance from Obscurity: Mammalian Rad52 in Homologous Recombination
por: Hanamshet, Kritika, et al.
Publicado: (2016)

Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes
por: Sadikovic, Bekim, et al.
Publicado: (2010)

Factors affecting template switch recombination associated with restarted DNA replication
por: Jalan, Manisha, et al.
Publicado: (2019)

LRF maintains genome integrity by regulating the non-homologous end joining pathway of DNA repair
por: Liu, Xue-Song, et al.
Publicado: (2015)

Cruciform DNA Structures Act as Legible Templates for Accelerating Homologous Recombination in Transgenic Animals
por: Ou-Yang, Huan, et al.
Publicado: (2022)

The Function of AID in Somatic Mutation and Class Switch Recombination: Upstream or Downstream of DNA Breaks
por: Chua, Katrin F., et al.
Publicado: (2002)

DNA-protein crosslinks are repaired via homologous recombination in mammalian mitochondria
por: Chesner, Lisa N., et al.
Publicado: (2020)

Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes
por: Sadikovic, Bekim, et al.
Publicado: (2017)

Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms
por: Malhotra, Ankit, et al.
Publicado: (2013)

Non-homologous end joining in class switch recombination: the beginning of the end
por: Kotnis, Ashwin, et al.
Publicado: (2008)

Sequence determinants of breakpoint location during HIV-1 intersubtype recombination
por: Baird, Heather A., et al.
Publicado: (2006)

Genome Sequence of Complex HIV-1 Unique Recombinant Forms Sharing a Common Recombination Breakpoint Identified in Malaysia
por: Cheong, Hui Ting, et al.
Publicado: (2015)

Repeat expansion in the budding yeast ribosomal DNA can occur independently of the canonical homologous recombination machinery
por: Houseley, Jonathan, et al.
Publicado: (2011)

PLK1 depletion alters homologous recombination and synaptonemal complex disassembly events during mammalian spermatogenesis
por: Wellard, Stephen R., et al.
Publicado: (2022)

RDR6-mediated synthesis of complementary RNA is terminated by miRNA stably bound to template RNA
por: Rajeswaran, Rajendran, et al.
Publicado: (2012)

Mating-type switching by homology-directed recombinational repair: a matter of choice
por: Thon, Geneviève, et al.
Publicado: (2018)

Rapid generation of long tandem DNA repeat arrays by homologous recombination in yeast to study their function in mammalian genomes
por: Noskov, Vladimir N, et al.
Publicado: (2011)

Evolution of gene regulation in ruminants differs between evolutionary breakpoint regions and homologous synteny blocks
por: Farré, Marta, et al.
Publicado: (2019)

Influence of sequence identity and unique breakpoints on the frequency of intersubtype HIV-1 recombination
por: Baird, Heather A, et al.
Publicado: (2006)

Heterozygous inversion breakpoints suppress meiotic crossovers by altering recombination repair outcomes
por: Li, Haosheng, et al.
Publicado: (2023)

Role for the Mammalian Swi5-Sfr1 Complex in DNA Strand Break Repair through Homologous Recombination
por: Akamatsu, Yufuko, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_frf22jdfdci8udomv941qnet9v