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Histone H4 acetylation analyses in patients with polysomy X: implications for the mechanism of X inactivation.

机译:X多形性患者的组蛋白H4乙酰化分析:对X失活机制的影响。

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摘要

In humans, it is thought that the X-inactivation phenomenon occurs no matter how many X chromosomes are present, and that only one of them remains active. Nevertheless, individuals who have an abnormal number of X chromosomes show a wide spectrum of abnormalities, which increase with the number of X chromosomes present in a given individual. It has been shown that the inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, and that this could be used as an accessible marker for distinguishing between Xi and Xa in spreads of metaphase chromosomes. We studied three X-polysomic patients for the presence of active chromatin by analysis of histone H4 acetylation on unfixed metaphase spreads. Using antisera to H4 acetylated at lysines 16, 8 and 5, respectively, we observed frequencies different from those expected from cells with only one underacetylated X chromosome. In particular, when antiserum to H4 acetylated at lysine 16 was used about 90% of the cells showed acetylation of all X chromosomes. This suggests a possible disturbance in the deacetylation process, probably due to the presence of multiple Xs.
机译:在人类中,人们认为无论存在多少X染色体,都会发生X灭活现象,并且其中只有一个保持活跃。但是,X染色体数目异常的个体显示出广泛的异常现象,该异常随着给定个体中X染色体数目的增加而增加。业已表明,雌性哺乳动物的无活性X染色体以缺乏组蛋白H4乙酰化为特征,并且可以用作区分中期染色体传播中Xi和Xa的可及标记。我们通过分析未固定中期扩散的组蛋白H4乙酰化,研究了三名X-多体障碍患者的活性染色质。分别使用针对在赖氨酸16、8和5处乙酰化的H4的抗血清,我们观察到的频率与只有一个未乙酰化的X染色体的细胞所预期的频率不同。特别地,当使用针对在赖氨酸16处乙酰化的H4的抗血清时,约90%的细胞显示所有X染色体的乙酰化。这表明脱乙酰过程中可能的干扰,可能是由于多个X的存在。

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