Bhat M A, Philp A V, Glover D M, Bellen H J
Howard Hughes Medical Institute, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.
Cell. 1996 Dec 13;87(6):1103-14. doi: 10.1016/s0092-8674(00)81804-8.
We have isolated a Drosophila gene, barren (barr), required for sister-chromatid segregation in mitosis. barr encodes a novel protein that is present in proliferating cells and has homologs in yeast and human. Mitotic defects in barr embryos become apparent during cycle 16, resulting in a loss of PNS and CNS neurons. Centromeres move apart at the metaphase-anaphase transition and Cyclin B is degraded, but sister chromatids remain connected, resulting in chromatin bridging. This phenotype is similar to that described in TOP2 mutants in yeast. Barren protein localizes to chromatin throughout mitosis. Colocalization and biochemical experiments indicate that Barren associates with Topoisomerase II throughout mitosis and alters the activity of Topoisomerase II. We propose that this association is required for proper chromosomal segregation by facilitating the decatenation of chromatids at anaphase.
我们分离出了一个果蝇基因——不育(barr)基因,它是有丝分裂中姐妹染色单体分离所必需的。barr基因编码一种新型蛋白质,这种蛋白质存在于增殖细胞中,在酵母和人类中也有同源物。barr胚胎中的有丝分裂缺陷在第16个细胞周期时变得明显,导致外周神经系统(PNS)和中枢神经系统(CNS)神经元缺失。在中期 - 后期转换时,着丝粒分开,细胞周期蛋白B降解,但姐妹染色单体仍保持连接,导致染色质桥接。这种表型与酵母中TOP2突变体所描述的表型相似。不育蛋白在整个有丝分裂过程中定位于染色质。共定位和生化实验表明,不育蛋白在整个有丝分裂过程中与拓扑异构酶II结合,并改变拓扑异构酶II的活性。我们认为,这种结合通过促进后期染色单体的解连环来实现正确的染色体分离。