NCAPG2 explained
Condensin-2 complex subunit G2 (CAP-G2) also known as chromosome-associated protein G2 (CAP-G2) or leucine zipper protein 5 (LUZP5) is a protein that in humans is encoded by the NCAPG2 gene.[1] [2] CAP-G2 is a subunit of condensin II, a large protein complex involved in chromosome condensation. It interacts with PLK1 through its C-terminal region during mitosis[3]
Clinical importance
Mutations in this gene in humans have been associated with severe neurodevelopmental defects, failure to thrive, ocular abnormalities, and defects in urogenital and limb morphogenesis.[4]
Further reading
- Smith ED, Xu Y, Tomson BN, Leung CG, Fujiwara Y, Orkin SH, Crispino JD . More than blood, a novel gene required for mammalian postimplantation development . Molecular and Cellular Biology . 24 . 3 . 1168–73 . February 2004 . 14729962 . 321451 . 10.1128/MCB.24.3.1168-1173.2004 .
- Nousiainen M, Silljé HH, Sauer G, Nigg EA, Körner R . Phosphoproteome analysis of the human mitotic spindle . Proceedings of the National Academy of Sciences of the United States of America . 103 . 14 . 5391–6 . April 2006 . 16565220 . 1459365 . 10.1073/pnas.0507066103 . 2006PNAS..103.5391N . free .
Notes and References
- Ono T, Losada A, Hirano M, Myers MP, Neuwald AF, Hirano T . Differential contributions of condensin I and condensin II to mitotic chromosome architecture in vertebrate cells . Cell . 115 . 1 . 109–21 . October 2003 . 14532007 . 10.1016/S0092-8674(03)00724-4 . 18811084 . free .
- Web site: Entrez Gene: NCAPG2 non-SMC condensin II complex, subunit G2.
- Kim JH, Shim J, Ji MJ, Jung Y, Bong SM, Jang YJ, Yoon EK, Lee SJ, Kim KG, Kim YH, Lee C, Lee BI, Kim KT . The condensin component NCAPG2 regulates microtubule-kinetochore attachment through recruitment of Polo-like kinase 1 to kinetochores . Nature Communications . 5 . 4588 . August 2014 . 25109385 . 10.1038/ncomms5588 . 2014NatCo...5.4588K . free .
- Khan TN, Khan K, Sadeghpour A, Reynolds H, Perilla Y, McDonald MT, Gallentine WB, Baig SM, Davis EE, Katsanis N . Task Force for Neonatal Genomics . Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of Condensinopathies . American Journal of Human Genetics . 104 . 1 . 94–111 . January 2019 . 30609410 . 10.1016/j.ajhg.2018.11.017 . 6323578 .