Hang Haiying, Zhang Yuzhu, Dunbrack Roland L, Wang Cuidong, Lieberman Howard B
Center for Radiological Research, Columbia University, 630 West 168th Street, New York, New York 10032, USA.
Genomics. 2002 Apr;79(4):487-92. doi: 10.1006/geno.2002.6737.
A paralog of the human cell cycle checkpoint gene HUS1 has been identified and designated HUS1B. It encodes a 278-amino-acid protein, 48% identical and 69% similar to HUS1. Mouse and rat orthologs of HUS1B have also been detected by a BLAST search. HUS1B is expressed variably in many human tissues, and the tissue-specific levels observed parallel those for HUS1. A HUS1-RAD1-RAD9 protein complex is thought to form a proliferating cell nuclear antigen (PCNA)-like structure, important for cell cycle checkpoint function. However, HUS1B directly interacts with RAD1, but not RAD9 or HUS1, whereas HUS1 can bind RAD1, RAD9, and another molecule of HUS1, suggesting that HUS1B cannot simply substitute for HUS1 in the complex. HUS1B is less conserved evolutionarily than HUS1. Furthermore, overexpression of HUS1B but not HUS1 in human cells induces clonogenic cell death. We suggest that HUS1B and HUS1 have distinct but related roles in regulating cell cycle checkpoints and genomic integrity.
已鉴定出人类细胞周期检查点基因HUS1的一个旁系同源基因,并将其命名为HUS1B。它编码一种278个氨基酸的蛋白质,与HUS1的同源性为48%,相似性为69%。通过BLAST搜索也检测到了HUS1B的小鼠和大鼠直系同源基因。HUS1B在许多人类组织中的表达存在差异,观察到的组织特异性水平与HUS1的水平相似。HUS1-RAD1-RAD9蛋白复合物被认为形成一种增殖细胞核抗原(PCNA)样结构,对细胞周期检查点功能很重要。然而,HUS1B直接与RAD1相互作用,但不与RAD9或HUS1相互作用,而HUS1可以结合RAD1、RAD9和另一个HUS1分子,这表明HUS1B不能简单地在复合物中替代HUS1。HUS1B在进化上的保守性低于HUS1。此外,在人类细胞中过表达HUS1B而非HUS1会诱导克隆源性细胞死亡。我们认为HUS1B和HUS1在调节细胞周期检查点和基因组完整性方面具有不同但相关的作用。