首页> 美国卫生研究院文献>American Journal of Human Genetics >Heritable fragile sites on human chromosomes. XI. Factors affecting expression of fragile sites at 10q25 16q22 and 17p12.
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Heritable fragile sites on human chromosomes. XI. Factors affecting expression of fragile sites at 10q25 16q22 and 17p12.

机译:人类染色体上的可遗传易碎位点。十一。影响10q25、16q22和17p12处易碎位点表达的因素。

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摘要

The fragile sites at 10q25, 16q22, and 17p12 can all be induced in lymphocyte culture by BrdU or BrdC added 6-12 hrs prior to harvest. Without induction, fra(10)(q25) is rarely expressed spontaneously, whereas fra(16)(q22) is frequently expressed spontaneously. Fra(17)(p12) is frequently expressed spontaneously but is probably expressed only after induction in some individuals. Distamycin A, netropsin, and Hoechst 33258 induced high levels of expression of fra(16)(q22) and fra(17)(p12) but did not enhance expression of fra(10)(q25). The mechanisms of induction of fra(16)(q22) by BrdU and distamycin A appear to be different, since the time of induction by BrdU reaches a maximum about 12 hrs prior to harvest whereas induction by distamycin A requires much longer exposure. The fragile sites at 10q25 and 16q22 were both induced in fibroblast culture by BrdU. Fra(17)(p12) is accepted as a fragile site because preliminary studies show that it behaves similarly in lymphocyte culture to fra(16)(q22); however, there is only limited evidence for fragility at 17p12.
机译:在收获前6-12小时加入BrdU或BrdC,可在淋巴细胞培养中诱导10q25、16q22和17p12处的脆弱位点。没有诱导,fra(10)(q25)很少自发表达,而fra(16)(q22)经常自发表达。 Fra(17)(p12)经常自发表达,但可能仅在某些个体中诱导后才表达。 Distamycin A,netropsin和Hoechst 33258诱导fra(16)(q22)和fra(17)(p12)的高水平表达,但并未增强fra(10)(q25)的表达。 BrdU和双歧霉素A诱导fra(16)(q22)的机制似乎有所不同,因为BrdU诱导的时间最多达到收获前约12小时,而双歧霉素A诱导则需要更长的时间。 BrdU在成纤维细胞培养中诱导了10q25和16q22处的脆弱位点。 Fra(17)(p12)被认为是脆弱的位点,因为初步研究表明它在淋巴细胞培养中的行为与fra(16)(q22)类似;但是,只有17p12的脆弱性证据有限。

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