Max-Planck-Institut für Immunbiologie, Freiburg im Breisgau, Germany.
Curr Opin Genet Dev. 2010 Apr;20(2):171-8. doi: 10.1016/j.gde.2010.01.007. Epub 2010 Feb 16.
X chromosomal regulation is a process that presents systematic problems of chromosome recognition and coordinated gene regulation. In Drosophila males, the ribonucleoprotein Male-Specific Lethal (MSL) complex plays an important role in hyperactivation of the X-linked genes to equalize gene dosage differences between the sexes. It appears that X chromosome recognition by the MSL complex may be mediated through a combination of sequence-specificity and transcriptional activities. The resulting transcriptional up-regulation also seems to involve several mechanisms, encompassing both gene-specific and chromosome-wide approaches. Interestingly the histone H4 lysine 16 specific MOF histone acetyl transferase, a key MSL member that hyper-acetylates the male X chromosome, is also involved in gene regulation beyond dosage compensation. A comparison of Drosophila and mammalian systems reveals intriguing parallels in MOF behavior, and highlights the multidisciplinary nature of this enzyme.
X 染色体调控是一个存在染色体识别和协调基因调控系统性问题的过程。在雄性果蝇中,核糖核蛋白 Male-Specific Lethal(MSL)复合物在 X 连锁基因的超活化中起着重要作用,以平衡性别之间的基因剂量差异。MSL 复合物对 X 染色体的识别似乎可以通过序列特异性和转录活性的组合来介导。由此产生的转录上调似乎也涉及几种机制,包括基因特异性和染色体广泛的方法。有趣的是,组蛋白 H4 赖氨酸 16 特异性 MOF 组蛋白乙酰转移酶,一种关键的 MSL 成员,可使雄性 X 染色体过度乙酰化,也参与了剂量补偿以外的基因调控。果蝇和哺乳动物系统的比较揭示了 MOF 行为的有趣相似之处,并强调了这种酶的多学科性质。