======= PARP2 ======= == Gene Information == * **Official Symbol**: PARP2 * **Official Name**: poly(ADP-ribose) polymerase 2 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=10038|10038]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q9UGN5|Q9UGN5]] * **Interactions**: [[https://thebiogrid.org/search.php?search=PARP2&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20PARP2|Open PubMed]] * **OMIM**: [[https://omim.org/entry/607725|Open OMIM]] == Function Summary == * **Entrez Summary**: This gene encodes poly(ADP-ribosyl)transferase-like 2 protein, which contains a catalytic domain and is capable of catalyzing a poly(ADP-ribosyl)ation reaction. This protein has a catalytic domain which is homologous to that of poly (ADP-ribosyl) transferase, but lacks an N-terminal DNA binding domain which activates the C-terminal catalytic domain of poly (ADP-ribosyl) transferase. The basic residues within the N-terminal region of this protein may bear potential DNA-binding properties, and may be involved in the nuclear and/or nucleolar targeting of the protein. Two alternatively spliced transcript variants encoding distinct isoforms have been found. [provided by RefSeq, Jul 2008]. * **UniProt Summary**: Involved in the base excision repair (BER) pathway, by catalyzing the poly(ADP-ribosyl)ation of a limited number of acceptor proteins involved in chromatin architecture and in DNA metabolism (PubMed:10364231, PubMed:28190768). This modification follows DNA damages and appears as an obligatory step in a detection/signaling pathway leading to the reparation of DNA strand breaks (PubMed:10364231). Mediates serine ADP-ribosylation of target proteins following interaction with HPF1; HPF1 conferring serine specificity (PubMed:28190768). {ECO:0000269|PubMed:10364231, ECO:0000269|PubMed:28190768}. |PARP| |PARP reg| |WGR| |NAD DNA ADP-ribosyltransferase activity| |DNA ADP-ribosylation| |peptidyl-serine ADP-ribosylation| |positive regulation of cell growth involved in cardiac muscle cell development| |protein poly-ADP-ribosylation| |protein ADP-ribosylase activity| |regulation of cell growth involved in cardiac muscle cell development| |positive regulation of cardiac muscle cell differentiation| |NAD+ ADP-ribosyltransferase activity| |positive regulation of cardiocyte differentiation| |positive regulation of cardiac muscle hypertrophy| |protein ADP-ribosylation| |positive regulation of muscle hypertrophy| |positive regulation of cardiac muscle tissue growth| |regulation of cardiac muscle cell differentiation| |positive regulation of heart growth| |base-excision repair| |positive regulation of cardiac muscle tissue development| |positive regulation of organ growth| |regulation of cardiocyte differentiation| |regulation of cardiac muscle hypertrophy| |positive regulation of striated muscle cell differentiation| |regulation of cardiac muscle tissue growth| |regulation of muscle hypertrophy| |regulation of heart growth| |positive regulation of muscle organ development| |positive regulation of striated muscle tissue development| |positive regulation of muscle tissue development| |regulation of cardiac muscle tissue development| |regulation of muscle adaptation| |positive regulation of muscle cell differentiation| |DNA modification| |regulation of organ growth| |extrinsic apoptotic signaling pathway| |regulation of striated muscle cell differentiation| |regulation of striated muscle tissue development| |regulation of muscle tissue development| |regulation of muscle organ development| |regulation of muscle cell differentiation| |positive regulation of cell growth| |positive regulation of developmental growth| |double-strand break repair| |peptidyl-serine modification| |negative regulation of neuron death| |regulation of muscle system process| |positive regulation of growth| |apoptotic signaling pathway| |regulation of neuron death| |regulation of developmental growth| |regulation of cell growth| |DNA repair| |positive regulation of cell development| |regulation of system process| |regulation of growth| |DNA metabolic process| |cellular response to DNA damage stimulus| |nucleolus| |peptidyl-amino acid modification| |apoptotic process| |regulation of cell development| |positive regulation of cell differentiation| |negative regulation of cell death| |programmed cell death| |cell death| |positive regulation of developmental process| |DNA binding| |regulation of cell death| |cellular response to stress| |positive regulation of multicellular organismal process| |regulation of cell differentiation| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp517|Quercetin 20μM R08 exp517]]|1.7| |[[:results:exp151|SGC0946 7μM R03 exp151]]|1.82| |[[:results:exp465|Cannabidiol 13μM R08 exp465]]|2.21| |[[:results:exp343|Centrinone 0.5μM R07 exp343]]|2.4| |[[:results:exp520|Rucaparib 6.5μM R08 exp520]]|2.74| |[[:results:exp501|Methotrexate 0.01μM R08 exp501]]|2.83| |[[:results:exp512|Olaparib 4μM R08 exp512]]|4.53| No correlation found to any other genes in chemogenomics. Global Fraction of Cell Lines Where Essential: 0/726 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/25| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/15| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/14| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/7| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 18478 * **Expression level (log2 read counts)**: 6.3 {{:chemogenomics:nalm6 dist.png?nolink |}}