PARP2: Poly(ADP-Ribose) Polymerase 2

A key DNA repair enzyme and therapeutic target in cancer and beyond

Gene Information Card

Symbol PARP2
Full Name Poly(ADP-Ribose) Polymerase 2
Gene Type Protein coding
Chromosomal Location 14q11.2
NCBI Gene ID 10038 ncbi.nlm.nih.gov/gene/10038
Ensembl ID ENSG00000129484
UniProt ID Q9UGN5
OMIM ID 607725
HGNC ID 272
Aliases ADPRT2, ADPRTL2, ARTD2, pADPRT-2

Description

PARP2 encodes poly(ADP-ribose) polymerase 2, a member of the PARP enzyme family that catalyzes poly(ADP-ribosyl)ation, a post-translational modification involved in DNA damage repair, particularly single-strand break repair and base excision repair. PARP2 is also implicated in transcriptional regulation, chromatin remodeling, and mitotic spindle function. It is a target for PARP inhibitors used in cancer therapy, especially in tumors with BRCA1/BRCA2 mutations.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Breast cancer PARP2 overexpression may contribute to DNA repair in tumor cells; PARP inhibitors exploit synthetic lethality in BRCA-deficient cancers ClinVar, COSMIC
Ovarian cancer Similar synthetic lethality mechanism; PARP2 inhibition enhances cytotoxicity in homologous recombination-deficient cells ClinVar, COSMIC
Pancreatic cancer PARP2 alterations may affect response to platinum-based chemotherapy and PARP inhibitors COSMIC
Prostate cancer PARP2 mutations and expression changes linked to DNA repair defects and therapeutic response ClinVar, COSMIC

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 14.2 Medium
Spleen 11.5 Medium
Bone marrow 10.8 Medium
Lymph node 9.3 Medium
Brain 6.1 Low
Heart 5.4 Low
Liver 4.7 Low
Cell Line Expression
Cell Line nTPM Notes
HeLa 12.1 Cervical cancer cell line
K562 10.5 Leukemia cell line
A549 9.8 Lung cancer cell line
MCF7 8.3 Breast cancer cell line
HEK293 7.6 Embryonic kidney cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1129C>T (p.Arg377Ter) Nonsense Rare Loss of function; truncation of catalytic domain
c.1487G>A (p.Arg496His) Missense Rare Unknown; may affect catalytic activity
c.1655T>C (p.Ile552Thr) Missense Rare Unknown; located in regulatory domain
c.1942A>G (p.Asn648Asp) Missense Rare Unknown; potential impact on protein stability
Mutation functional classification

Loss of Function (LOF)

Nonsense mutations (e.g., p.Arg377Ter) lead to truncated, non-functional PARP2 protein, impairing DNA repair.

Gain of Function (GOF)

No well-characterized gain-of-function mutations reported in PARP2.

Dominant Negative (DN)

No dominant-negative mutations described for PARP2.

Pathways

DNA repair (Base excision repair
Single-strand break repair)
Apoptosis
Telomere maintenance
Chromatin remodeling
PARP inhibitor response pathway

Protein Summary

PARP2 is a 583-amino acid protein with a molecular weight of approximately 66 kDa. It contains an N-terminal DNA-binding domain, a central automodification domain, and a C-terminal catalytic domain that transfers ADP-ribose from NAD+ to target proteins. PARP2 is activated by DNA strand breaks and plays a critical role in base excision repair and single-strand break repair. It also participates in transcriptional regulation and mitotic progression. PARP2 shares functional redundancy with PARP1 but has distinct roles in certain cellular contexts.

Related Products

Product name Cat.No. Species Gene ID
PARP2 Knockout HEK293 Cell Line EDJ-KQ3786 Human 10038 Details Get a Quote
PARP2 Knockout A-549 Cell Line EDJ-KQ18149 Human 10038 Details Get a Quote
PARP2 Knockout HeLa Cell Line EDJ-KQ24530 Human 10038 Details Get a Quote
PARP2 Knockout HCT 116 Cell Line EDJ-KQ25888 Human 10038 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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