Zhang Xiao-Yong, Varthi Maya, Sykes Stephen M, Phillips Charles, Warzecha Claude, Zhu Wenting, Wyce Anastasia, Thorne Alan W, Berger Shelley L, McMahon Steven B
The Department of Cancer Biology, The Kimmel Cancer Center, Thomas Jefferson Medical College, Philadelphia, PA 19107, USA.
Mol Cell. 2008 Jan 18;29(1):102-11. doi: 10.1016/j.molcel.2007.12.015.
Polycomb genes encode critical regulators of both normal stem cells and cancer stem cells. A gene signature that includes Polycomb genes and additional genes coregulated with Polycomb genes was recently identified. The expression of this signature has been reported to identify tumors with the cancer stem cell phenotypes of aggressive growth, metastasis, and therapy resistance. Most members of this 11 gene signature encode proteins with well-defined roles in human cancer. However, the function of the signature member USP22 remains unknown. We report that USP22 is a previously uncharacterized subunit of the human SAGA transcriptional cofactor complex. Within SAGA, USP22 deubiquitylates histone H2B. Furthermore, USP22 is recruited to specific genes by activators such as the Myc oncoprotein, where it is required for transcription. In support of a functional role within the Polycomb/cancer stem cell signature, USP22 is required for appropriate progression through the cell cycle.
多梳基因编码正常干细胞和癌症干细胞的关键调节因子。最近鉴定出了一个包括多梳基因以及与多梳基因共同调控的其他基因的基因特征。据报道,该特征的表达可识别具有侵袭性生长、转移和治疗抗性等癌症干细胞表型的肿瘤。这个11基因特征的大多数成员编码在人类癌症中具有明确作用的蛋白质。然而,该特征成员USP22的功能仍然未知。我们报告称,USP22是人类SAGA转录辅因子复合物中一个以前未被描述的亚基。在SAGA中,USP22使组蛋白H2B去泛素化。此外,USP22被激活剂(如Myc癌蛋白)招募到特定基因,在那里它是转录所必需的。为支持其在多梳/癌症干细胞特征中的功能作用,USP22是细胞周期正常进展所必需的。