Bhadra Manika Pal, Bhadra Utpal, Kundu Joydeep, Birchler James A
Division of Biological Sciences, University of Missouri, Columbia, 65211, USA.
Genetics. 2005 Apr;169(4):2061-74. doi: 10.1534/genetics.104.036020. Epub 2005 Feb 16.
Dosage compensation refers to the equal expression of X-linked genes despite the difference in copy number between the two sexes. The male-specific lethal (MSL) complex is concentrated on the X chromosome in males. A gene expression assay for embryos was developed to examine the function of this complex. In mutant male embryos without either the MSL complex or MOF histone acetylase, dosage compensation is retained but autosomal expression is increased. Dosage compensation is lost in the double-mutant embryos. In embryos in which the MSL complex and MOF are targeted to the X chromosomes in females, the results are consistent with previous surveys showing that in general the X expression remains unchanged, but autosomal expression is reduced. Mutations in the ISWI chromatin-remodeling component cause increases specifically of X-linked genes in males. Thus, the function of the MSL complex in conjunction with ISWI is postulated to override the effect on gene expression of high histone acetylation on the male X. The basic determinant of dosage compensation is suggested to be an inverse dosage effect produced by an imbalance of transcription factors on the X vs. the autosomes. The sequestration of the MSL complex to the male X may have evolved to counteract a similar effect on the autosomes and to prevent an overexpression of the X chromosome in males that would otherwise occur due to the high levels of histone acetylation.
剂量补偿是指尽管两性之间X连锁基因的拷贝数存在差异,但这些基因仍能等量表达。雄性特异性致死(MSL)复合物在雄性个体中集中于X染色体上。为了研究该复合物的功能,开发了一种针对胚胎的基因表达检测方法。在没有MSL复合物或MOF组蛋白乙酰转移酶的突变雄性胚胎中,剂量补偿得以保留,但常染色体表达增加。在双突变胚胎中,剂量补偿丧失。在雌性胚胎中,若MSL复合物和MOF靶向于X染色体,其结果与之前的研究一致,即一般情况下X染色体的表达保持不变,但常染色体表达减少。ISWI染色质重塑成分的突变会导致雄性个体中X连锁基因特异性增加。因此,推测MSL复合物与ISWI共同作用,能够克服高组蛋白乙酰化对雄性X染色体上基因表达的影响。剂量补偿的基本决定因素被认为是X染色体与常染色体上转录因子失衡所产生的反向剂量效应。MSL复合物定位于雄性X染色体上,可能是为了抵消对常染色体的类似影响,并防止雄性个体中X染色体因组蛋白乙酰化水平过高而出现过表达。