Department of Molecular, Cell, and Developmental Biology, University of California Santa Cruz, Santa Cruz, California, United States of America.
PLoS Genet. 2012;8(8):e1002878. doi: 10.1371/journal.pgen.1002878. Epub 2012 Aug 9.
dMi-2 is a highly conserved ATP-dependent chromatin-remodeling factor that regulates transcription and cell fates by altering the structure or positioning of nucleosomes. Here we report an unanticipated role for dMi-2 in the regulation of higher-order chromatin structure in Drosophila. Loss of dMi-2 function causes salivary gland polytene chromosomes to lose their characteristic banding pattern and appear more condensed than normal. Conversely, increased expression of dMi-2 triggers decondensation of polytene chromosomes accompanied by a significant increase in nuclear volume; this effect is relatively rapid and is dependent on the ATPase activity of dMi-2. Live analysis revealed that dMi-2 disrupts interactions between the aligned chromatids of salivary gland polytene chromosomes. dMi-2 and the cohesin complex are enriched at sites of active transcription; fluorescence-recovery after photobleaching (FRAP) assays showed that dMi-2 decreases stable association of cohesin with polytene chromosomes. These findings demonstrate that dMi-2 is an important regulator of both chromosome condensation and cohesin binding in interphase cells.
dMi-2 是一种高度保守的 ATP 依赖的染色质重塑因子,通过改变核小体的结构或定位来调节转录和细胞命运。在这里,我们报告了 dMi-2 在调控果蝇中高级染色质结构中的一个意外作用。dMi-2 功能的丧失导致唾液腺多线染色体失去其特征性带型,并且比正常情况下更浓缩。相反,dMi-2 的表达增加会引发多线染色体的去浓缩,同时核体积显著增加;这种效应相对较快,并且依赖于 dMi-2 的 ATP 酶活性。实时分析显示,dMi-2 破坏了唾液腺多线染色体中对齐的染色单体之间的相互作用。dMi-2 和黏合蛋白复合物在活跃转录的位点富集;荧光恢复后光漂白(FRAP)实验表明,dMi-2 降低了黏合蛋白与多线染色体的稳定结合。这些发现表明,dMi-2 是有丝分裂细胞中染色体浓缩和黏合蛋白结合的重要调节剂。