Interaction between antibody-diversification enzyme AID and spliceosome-associated factor CTNNBL1 (Q24336265)

GOA release 2020-03-11

Catenin beta like 1

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somatic diversification of immunoglobulins

GOA release 2020-03-11

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GOA release 2020-03-11

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Kanmin Xue

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Silvestro G. Conticello

object named as

Silvestro G Conticello

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author name string

Karuna Ganesh

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Mason Lu

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Cristina Rada

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Michael S Neuberger

Light chain gene conversion continues at high rate in an ALV-induced cell line.

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language of work or name

English

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publication date

22 August 2008

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474-84

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cites work

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The Prp19/Pso4 core complex undergoes ubiquitylation and structural alterations in response to DNA damage

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AID in somatic hypermutation and class switch recombination

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Cotranscriptional spliceosome assembly occurs in a stepwise fashion and requires the cap binding complex

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Recognition of trimethylated histone H3 lysine 4 facilitates the recruitment of transcription postinitiation factors and pre-mRNA splicing

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A 5' splice site enhances the recruitment of basal transcription initiation factors in vivo.

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Class switch recombination and hypermutation require activation-induced cytidine deaminase (AID), a potential RNA editing enzyme

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Sequence, gene structure, and expression pattern of CTNNBL1, a minor-class intron-containing gene--evidence for a role in apoptosis

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AID is essential for immunoglobulin V gene conversion in a cultured B cell line

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The ras recruitment system, a novel approach to the study of protein-protein interactions

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Armadillo repeat proteins: beyond the animal kingdom

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Ablation of XRCC2/3 transforms immunoglobulin V gene conversion into somatic hypermutation

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AID mutates E. coli suggesting a DNA deamination mechanism for antibody diversification

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The AID antibody diversification enzyme is regulated by protein kinase A phosphorylation

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Targeting of somatic hypermutation

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mRNA processing and genomic instability

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A subset of human 35S U5 proteins, including Prp19, function prior to catalytic step 1 of splicing

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Plat-E: an efficient and stable system for transient packaging of retroviruses

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Activation-induced cytidine deaminase shuttles between nucleus and cytoplasm like apolipoprotein B mRNA editing catalytic polypeptide 1

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PKA-mediated phosphorylation regulates the function of activation-induced deaminase (AID) in B cells

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Regulation of hypermutation by activation-induced cytidine deaminase phosphorylation

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AID-GFP chimeric protein increases hypermutation of Ig genes with no evidence of nuclear localization

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In Vitro Deamination of Cytosine to Uracil in Single-stranded DNA by Apolipoprotein B Editing Complex Catalytic Subunit 1 (APOBEC1)

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Activation-induced cytosine deaminase (AID) is actively exported out of the nucleus but retained by the induction of DNA breaks

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Human Pso4 is a metnase (SETMAR)-binding partner that regulates metnase function in DNA repair

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Processing of switch transcripts is required for targeting of antibody class switch recombination

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Somatic hypermutation is limited by CRM1-dependent nuclear export of activation-induced deaminase

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Mutational comparison of the single-domained APOBEC3C and double-domained APOBEC3F/G anti-retroviral cytidine deaminases provides insight into their DNA target site specificities

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Cotranscriptional processes and their influence on genome stability.

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Requirement of the activation-induced deaminase (AID) gene for immunoglobulin gene conversion

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Cotranscriptional recruitment of the U1 snRNP to intron-containing genes in yeast

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Molecular mechanisms of antibody somatic hypermutation.

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Expression of the AID protein in normal and neoplastic B cells

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Multiple links between transcription and splicing

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Activation-induced cytidine deaminase initiates immunoglobulin gene conversion and hypermutation by a common intermediate

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