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染色体领地、X;Y易位与卵巢早衰:它们之间有关联吗?

Chromosome territories, X;Y translocation and Premature Ovarian Failure: is there a relationship?

作者信息

Lissoni Sara, Baronchelli Simona, Villa Nicoletta, Lucchini Valeria, Betri Enrico, Cavalli Pietro, Dalprà Leda

机构信息

Department of Neuroscience and Biomedical Technologies, University of Milan-Bicocca, via Cadore 48, 20052, Monza, Italy.

出版信息

Mol Cytogenet. 2009 Sep 27;2:19. doi: 10.1186/1755-8166-2-19.

Abstract

BACKGROUND

Premature ovarian failure (POF) is a secondary hypergonadotrophic amenorrhea occurring before the age of 40 and affecting 1-3% of females. Chromosome anomalies account for 6-8% of POF cases, but only few cases are associated with translocations involving X and Y chromosomes.This study shows the cytogenetic and molecular analysis of a POF patient came to our attention as she developed a left ovary choriocarcinoma at the age of 10 and at 14 years of age she presented secondary amenorrhea with elevated levels of gonadotropins.

RESULTS

Breakpoint position on X and Y chromosomes was investigated using Fluorescent In Situ Hybridisation (FISH) with a panel of specific BAC probes, microsatellite analysis and evaluation of copy number changes and loss of heterozigosity by Affymetrix(R) GeneChip platform (Santa Clara, CA, USA). Patient's karyotype resulted 46, X, der(Y)t(X;Y)(q13.1;q11.223). X inactivation study was assessed by RBA banding and showed preferential inactivation of derivative chromosome. The reciprocal spatial disposition of sexual chromosome territories was investigated using whole chromosome painting and centromeres probes: patient's results didn't show a significant difference in comparison to normal controls.

CONCLUSION

The peculiar clinical case come to our attention highlighted the complexity of POF aetiology and of the translocation event, even if our results seem to exclude any effect on nuclear organisation. POF phenotype could be partially explained by skewed X chromosome inactivation that influences gene expression.

摘要

背景

卵巢早衰(POF)是一种发生在40岁之前的继发性高促性腺激素性闭经,影响1%-3%的女性。染色体异常占POF病例的6%-8%,但只有少数病例与涉及X和Y染色体的易位有关。本研究展示了对一名POF患者的细胞遗传学和分子分析,该患者因10岁时患左卵巢绒毛膜癌且14岁时出现继发性闭经、促性腺激素水平升高而引起我们的注意。

结果

使用一组特定的BAC探针通过荧光原位杂交(FISH)、微卫星分析以及利用Affymetrix® GeneChip平台(美国加利福尼亚州圣克拉拉)评估拷贝数变化和杂合性缺失,研究X和Y染色体上的断点位置。患者的核型结果为46, X, der(Y)t(X;Y)(q13.1;q11.223)。通过RBA显带评估X染色体失活研究,结果显示衍生染色体优先失活。使用全染色体涂染和着丝粒探针研究性染色体区域的相互空间分布:与正常对照相比,患者的结果未显示出显著差异。

结论

引起我们注意的这个特殊临床病例突出了POF病因以及易位事件的复杂性,即便我们的结果似乎排除了对核组织的任何影响。POF表型可能部分由影响基因表达的X染色体失活偏斜来解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d538/2761935/e5f286aaf3e0/1755-8166-2-19-1.jpg

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