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果蝇雄性X染色体上的乙酰化组蛋白H4与剂量补偿相关。

Acetylated histone H4 on the male X chromosome is associated with dosage compensation in Drosophila.

作者信息

Bone J R, Lavender J, Richman R, Palmer M J, Turner B M, Kuroda M I

机构信息

Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Genes Dev. 1994 Jan;8(1):96-104. doi: 10.1101/gad.8.1.96.

Abstract

Dosage compensation in Drosophila occurs by an increase in transcription of genes on the X chromosome in males. This elevated expression requires the function of at least four loci, known collectively as the male-specific lethal (msl) genes. The proteins encoded by two of these genes, maleless (mle) and male-specific lethal-1 (msl-1), are found associated with the X chromosome in males, suggesting that they act as positive regulators of dosage compensation. A specific acetylated isoform of histone H4, H4Ac16, is also detected predominantly on the male X chromosome. We have found that MLE and MSL-1 bind to the X chromosome in an identical pattern and that the pattern of H4Ac16 on the X is largely coincident with that of MLE/MSL-1. We fail to detect H4Ac16 on the X chromosome in homozygous msl males, correlating with the lack of dosage compensation in these mutants. Conversely, in Sxl mutants, we detect H4Ac16 on the female X chromosomes, coincident with an inappropriate increase in X chromosome transcription. These data suggest that synthesis or localization of H4Ac16 is controlled by the dosage compensation regulatory hierarchy. Dosage compensation may involve H4Ac16 function, potentially through interaction with the product of the msl genes.

摘要

果蝇中的剂量补偿是通过雄性X染色体上基因转录的增加来实现的。这种增强的表达需要至少四个位点的功能,这些位点统称为雄性特异性致死(msl)基因。其中两个基因编码的蛋白质,无雄性(mle)和雄性特异性致死-1(msl-1),在雄性中与X染色体相关联,这表明它们作为剂量补偿的正调控因子发挥作用。一种特定的组蛋白H4乙酰化异构体,H4Ac16,也主要在雄性X染色体上被检测到。我们发现MLE和MSL-1以相同的模式与X染色体结合,并且X染色体上H4Ac16的模式与MLE/MSL-1的模式基本一致。我们在纯合msl雄性的X染色体上未检测到H4Ac16,这与这些突变体中剂量补偿的缺失相关。相反,在Sxl突变体中,我们在雌性X染色体上检测到H4Ac16,这与X染色体转录的不适当增加一致。这些数据表明H4Ac16的合成或定位受剂量补偿调控层次的控制。剂量补偿可能涉及H4Ac16的功能,可能是通过与msl基因的产物相互作用。

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