Proteomics

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Defining the NSD2 interactome: PARP1 PARylation reduces NSD2 histone methyltransferase activity and impedes chromatin binding


ABSTRACT: NSD2 is a histone methyltransferase that specifically dimethylates histone H3 lysine 36 (H3K36me2), a modification associated with gene activation. Dramatic overexpression of NSD2 in t(4;14) multiple myeloma (MM) and an activating mutation of NSD2 discovered in acute lymphoblastic leukemia (ALL) are significantly associated with altered gene activation, transcription and DNA damage repair. The partner proteins through which NSD2 may influence critical cellular processes remain poorly defined. In this study, we utilized proximity-based labelling (BioID) combined with label-free quantitative mass spectrometry to identify high confidence NSD2 interacting partners in MM cells.

INSTRUMENT(S): LTQ Orbitrap Velos

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Blood Cell, Bone Marrow

SUBMITTER: Xiaoxiao Huang  

LAB HEAD: Neil L Kelleher

PROVIDER: PXD013759 | Pride | 2019-06-27

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
Study1_NSD2BirA_bio1.mgf Mgf
Study1_NSD2BirA_bio1.mzid.gz Mzid
Study1_NSD2BirA_bio1.pride.mgf.gz Mgf
Study1_NSD2BirA_bio1.pride.mztab.gz Mztab
Study1_NSD2BirA_bio1.raw Raw
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Publications

Defining the NSD2 interactome: PARP1 PARylation reduces NSD2 histone methyltransferase activity and impedes chromatin binding.

Huang Xiaoxiao X   LeDuc Richard D RD   Fornelli Luca L   Schunter Alissa J AJ   Bennett Richard L RL   Kelleher Neil L NL   Licht Jonathan D JD  

The Journal of biological chemistry 20190627 33


NSD2 is a histone methyltransferase that specifically dimethylates histone H3 lysine 36 (H3K36me2), a modification associated with gene activation. Dramatic overexpression of NSD2 in t(4;14) multiple myeloma (MM) and an activating mutation of NSD2 discovered in acute lymphoblastic leukemia are significantly associated with altered gene activation, transcription, and DNA damage repair. The partner proteins through which NSD2 may influence critical cellular processes remain poorly defined. In this  ...[more]

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