Ewen M E, Xing Y G, Lawrence J B, Livingston D M
Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115.
Cell. 1991 Sep 20;66(6):1155-64. doi: 10.1016/0092-8674(91)90038-z.
p107 is a cellular protein that forms specific complexes with adenovirus E1A and SV40 large T antigen (T). The genetics of the p107-T/E1A interaction as well as other features of this protein suggests that p107 shares functional properties with the tumor suppressor product, RB. A partial cDNA for human p107 has been cloned. Its sequences map to 20q11.2 and encode a 936 residue protein. Comparison analysis of the p107 protein sequence reveals a major region of RB homology extending over 564 residues. This region in RB is essential to its growth-controlling function. Sequences outside of these two regions are largely unique to each protein. The p107 and RB homology regions can independently bind to T and E1A. Thus, these two proteins display similarities of structure that may, at least in part, explain their known functional similarities and suggest a generic function for p107 in cell cycle regulation.
p107是一种细胞蛋白,它与腺病毒E1A及猿猴病毒40大T抗原(T)形成特定复合物。p107与T/E1A相互作用的遗传学以及该蛋白的其他特性表明,p107与肿瘤抑制产物RB具有功能特性。人p107的部分cDNA已被克隆。其序列定位于20q11.2,编码一个含936个残基的蛋白质。对p107蛋白序列的比较分析揭示了一个与RB同源的主要区域,该区域延伸超过564个残基。RB中的这一区域对其生长控制功能至关重要。这两个区域之外的序列在很大程度上是每种蛋白质所特有的。p107和RB的同源区域可独立结合T和E1A。因此,这两种蛋白质显示出结构上的相似性,这至少在一定程度上可以解释它们已知的功能相似性,并提示p107在细胞周期调控中具有一般功能。