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使用富含AT的DNA结合化学物质增强继发性闭经女性中FRA16B的表达。

Enhanced Expression of FRA16B using AT-Rich DNA Binding Chemicals in a Woman with Secondary Amenorrhoea.

作者信息

Bhavani Gunasekaran, Sivaprakash S, Samuel Chandra R, Santhiya Sathiyavedu Thyagarajan

机构信息

Ph.D. Research Scholar, Department of of Genetics, Dr. ALM Postgraduate Institute of Basic Medical Sciences, University of Madras, Taramani, Chennai, Tamil Nadu, India.

Assistant Professor, Department of Endocrinology and Diabetology, Institute of Obstetrics and Gynaecology, Government Hospital for Women and Children, Egmore, Chennai, Tamil Nadu, India.

出版信息

J Clin Diagn Res. 2017 Jun;11(6):QD01-QD03. doi: 10.7860/JCDR/2017/26545.10043. Epub 2017 Jun 1.

Abstract

Fragile sites represent regions of chromatin that fail to compact during mitosis. Based on the prevalence and pattern of inheritance they are classified as rare fragile sites or common fragile sites. Rare fragile sites either occur spontaneously or can be induced by certain AT-specific binding chemicals namely distamycin, Hoechst 33258, Berenil and others. The most common of all rare autosomal fragile sites is fra(16)(q22) with a heterozygote frequency of ~5%. FRA16B results from an expansion of a 33 bp AT-rich Minisatellite repeat. These rare forms are usually heritable and segregate in a Mendelian fashion. The proband who was referred for secondary amenorrhoea, revealed 46,XX,fra(16)(q22.1)pat karyotype. Her father and younger sibling were also found to be carriers. This study aimed to delineate the genotypic and phenotypic features exhibited by these carriers and to evaluate FRA16B expression using AT-specific binding chemicals. The additives employed were Berenil, BrdU and Hoechst 33258. Berenil at a concentration of 150 µg/ml showed the highest expression of FRA16B. Although the recent breakthrough in molecular characterization of fragile sites plays a critical role in comprehending their association with various diseases, the physiological link between them and amenorrhoea is not clearly understood.

摘要

脆性位点代表染色质中在有丝分裂期间无法紧密压缩的区域。根据其发生率和遗传模式,它们被分为罕见脆性位点或常见脆性位点。罕见脆性位点要么自发出现,要么可由某些特异性结合AT的化学物质诱导产生,即偏端霉素、Hoechst 33258、贝尼尔等。所有罕见常染色体脆性位点中最常见的是fra(16)(q22),杂合子频率约为5%。FRA16B源于一个33 bp富含AT的小卫星重复序列的扩增。这些罕见形式通常是可遗传的,并以孟德尔方式分离。因继发性闭经前来就诊的先证者,其核型为46,XX,fra(16)(q22.1)pat。还发现她的父亲和弟弟也是携带者。本研究旨在描述这些携带者所表现出的基因型和表型特征,并使用特异性结合AT的化学物质评估FRA16B的表达。所使用的添加剂为贝尼尔、溴脱氧尿苷和Hoechst 33258。浓度为150 µg/ml的贝尼尔显示出FRA16B的最高表达。尽管最近在脆性位点的分子特征方面取得的突破在理解它们与各种疾病的关联中起着关键作用,但它们与闭经之间的生理联系尚不清楚。

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