IgH class switching and translocations use a robust non-classical end-joining pathway (Q28241679)

Activation-induced cytidine deaminase

GOA release 2020-03-11

1 reference

X-ray repair complementing defective repair in Chinese hamster cells 4

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

8

Mark Geyer

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Klaus Rajewsky

object named as

Klaus Rajewsky

11

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author name string

Catherine T Yan

1

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Cristian Boboila

2

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Ellen Kris Souza

3

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Sonia Franco

4

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Thomas R Hickernell

5

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Michael Murphy

6

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Sunil Gumaste

7

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Ali A Zarrin

9

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John P Manis

10

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Frederick W Alt

Evolution of the immunoglobulin heavy chain class switch recombination mechanism

12

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language of work or name

English

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publication date

27 September 2007

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published in

Nature

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volume

449

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issue

7161

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page(s)

478-82

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cites work

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Different types of V(D)J recombination and end-joining defects in DNA double-strand break repair mutant mammalian cells

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Ku70 is required for late B cell development and immunoglobulin heavy chain class switching

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Ku80 is required for immunoglobulin isotype switching

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H2AX is required for recombination between immunoglobulin switch regions but not for intra-switch region recombination or somatic hypermutation

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Impact of DNA ligase IV on nonhomologous end joining pathways during class switch recombination in human cells.

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A critical role for DNA end-joining proteins in both lymphogenesis and neurogenesis

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XRCC4 suppresses medulloblastomas with recurrent translocations in p53-deficient mice

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Interplay of p53 and DNA-repair protein XRCC4 in tumorigenesis, genomic stability and development

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Survival of resting mature B lymphocytes depends on BCR signaling via the Igalpha/beta heterodimer

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Antibody class switching mediated by yeast endonuclease-generated DNA breaks.

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Absence of DNA ligase IV protein in XR-1 cells: evidence for stabilization by XRCC4.

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Late embryonic lethality and impaired V(D)J recombination in mice lacking DNA ligase IV

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H2AX prevents DNA breaks from progressing to chromosome breaks and translocations

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DNA ligase III as a candidate component of backup pathways of nonhomologous end joining

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Amplifying mechanisms of lymphomagenesis

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Double-strand break repair in Ku86- and XRCC4-deficient cells

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Impact of the KU80 pathway on NHEJ-induced genome rearrangements in mammalian cells.

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Unrepaired DNA breaks in p53-deficient cells lead to oncogenic gene amplification subsequent to translocations.

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Involvement of poly(ADP-ribose) polymerase-1 and XRCC1/DNA ligase III in an alternative route for DNA double-strand breaks rejoining.

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Rejoining of DNA double-strand breaks as a function of overhang length

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XRCC4:DNA ligase IV can ligate incompatible DNA ends and can ligate across gaps

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Role for mismatch repair proteins Msh2, Mlh1, and Pms2 in immunoglobulin class switching shown by sequence analysis of recombination junctions

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Switch junction sequences in PMS2-deficient mice reveal a microhomology-mediated mechanism of Ig class switch recombination.

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Lack of N regions in antigen receptor variable region genes of TdT-deficient lymphocytes

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Accurate in vitro end joining of a DNA double strand break with partially cohesive 3'-overhangs and 3'-phosphoglycolate termini: effect of Ku on repair fidelity

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Modeling oncogenic translocations: distinct roles for double-strand break repair pathways in translocation formation in mammalian cells

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Radiosensitization of MDA-MB-231 breast tumor cells by adenovirus-mediated overexpression of a fragment of the XRCC4 protein

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IgH class switch recombination to IgG1 in DNA-PKcs-deficient B cells

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inferred from DOI database lookup

7 January 2021

based on heuristic

Rag mutations reveal robust alternative end joining

1 reference

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