Schaaf Cheri A, Misulovin Ziva, Sahota Gurmukh, Siddiqui Akbar M, Schwartz Yuri B, Kahn Tatyana G, Pirrotta Vincenzo, Gause Maria, Dorsett Dale
Edward A. Doisy Department of Biochemistry and Molecular Biology, Saint Louis University School of Medicine, Saint Louis, Missouri, USA.
PLoS One. 2009 Jul 9;4(7):e6202. doi: 10.1371/journal.pone.0006202.
The cohesin protein complex was first recognized for holding sister chromatids together and ensuring proper chromosome segregation. Cohesin also regulates gene expression, but the mechanisms are unknown. Cohesin associates preferentially with active genes, and is generally absent from regions in which histone H3 is methylated by the Enhancer of zeste [E(z)] Polycomb group silencing protein. Here we show that transcription is hypersensitive to cohesin levels in two exceptional cases where cohesin and the E(z)-mediated histone methylation simultaneously coat the entire Enhancer of split and invected-engrailed gene complexes in cells derived from Drosophila central nervous system. These gene complexes are modestly transcribed, and produce seven of the twelve transcripts that increase the most with cohesin knockdown genome-wide. Cohesin mutations alter eye development in the same manner as increased Enhancer of split activity, suggesting that similar regulation occurs in vivo. We propose that cohesin helps restrain transcription of these gene complexes, and that deregulation of similarly cohesin-hypersensitive genes may underlie developmental deficits in Cornelia de Lange syndrome.
黏连蛋白复合体最初因将姐妹染色单体结合在一起并确保染色体正确分离而被识别。黏连蛋白也调节基因表达,但其机制尚不清楚。黏连蛋白优先与活跃基因结合,并且通常不存在于由zeste增强子[E(z)]多梳家族沉默蛋白使组蛋白H3甲基化的区域。在这里,我们表明,在两种特殊情况下,转录对黏连蛋白水平高度敏感,即黏连蛋白和E(z)介导的组蛋白甲基化同时覆盖果蝇中枢神经系统来源细胞中的整个split增强子和invected-engrailed基因复合体。这些基因复合体适度转录,并产生全基因组范围内随着黏连蛋白敲低增加最多的十二个转录本中的七个。黏连蛋白突变以与split增强子活性增加相同的方式改变眼睛发育,这表明体内发生类似的调控。我们提出,黏连蛋白有助于抑制这些基因复合体的转录,并且类似黏连蛋白超敏基因的失调可能是科妮莉亚·德·朗格综合征发育缺陷的基础。