The retinoblastoma protein (protein name abbreviated pRb; gene name abbreviated Rb, RB or RB1) is a tumor suppressor protein that is dysfunctional in several major cancers.[5] One function of pRb is to prevent excessive cell growth by inhibiting cell cycle progression until a cell is ready to divide. When the cell is ready to divide, pRb is phosphorylated, inactivating it, and the cell cycle is allowed to progress. It is also a recruiter of several chromatin remodeling enzymes such as methylases and acetylases.[6]
pRb belongs to the pocket protein family, whose members have a pocket for the functional binding of other proteins.[7][8] Should an oncogenic protein, such as those produced by cells infected by high-risk types of human papillomavirus, bind and inactivate pRb, this can lead to cancer. The RBgene may have been responsible for the evolution of multicellularity in several lineages of life including animals.[9]
https://en.wikipedia.org/wiki/Retinoblastoma_protein
vte
Tumor suppressor genes and Oncogenes
showvte
Cell cycle proteins
Categories: Genes on human chromosome 9
No comments:
Post a Comment