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监测自然种群中的诱导遗传性突变:微卫星DNA筛选的应用

Monitoring for induced heritable mutations in natural populations: application of minisatellite DNA screening.

作者信息

Yauk C

机构信息

Dept. of Biology, McMaster University, Hamilton, ON, Canada.

出版信息

Mutat Res. 1998 Aug;411(1):1-10. doi: 10.1016/s1383-5742(98)00003-9.

Abstract

The need to understand the role that anthropogenic chemicals play in generating germline mutations is critical, both from an ecological and a human health perspective. Exposure to complex mixtures of urban and industrial chemicals is widespread and we have little understanding of the long-term implications to populations and gene pools. It has recently been suggested that minisatellite DNA mutations may be sensitive biomarkers for induced heritable mutations in populations exposed to radioactive and non-radioactive contamination in their environments. Minisatellite loci are attractive targets for mutational analyses because they undergo a rate of mutation much greater than unique sequence DNA and with DNA fingerprinting many loci can be scanned simultaneously. As a result, the technique is statistically powerful requiring relatively small sample sizes (compared to other in situ mutation assays) and is reasonably cost and time efficient. This paper will review the application of minisatellite mutation screening to the field of genetic toxicology.

摘要

从生态和人类健康的角度来看,了解人为化学物质在产生生殖系突变中所起的作用至关重要。城市和工业化学物质的复杂混合物暴露十分普遍,而我们对其对种群和基因库的长期影响却知之甚少。最近有人提出,微卫星DNA突变可能是在环境中暴露于放射性和非放射性污染的人群中诱导遗传性突变的敏感生物标志物。微卫星位点是突变分析的有吸引力的目标,因为它们的突变率远高于独特序列DNA,并且通过DNA指纹技术可以同时扫描多个位点。因此,该技术在统计学上具有强大的功效,所需样本量相对较小(与其他原位突变检测相比),并且具有合理的成本和时间效率。本文将综述微卫星突变筛选在遗传毒理学领域的应用。

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