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传递率失真:概念回顾及其对遗传关联研究的意义。

Transmission ratio distortion: review of concept and implications for genetic association studies.

机构信息

Department of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, QC H3A 1A2, Canada.

出版信息

Hum Genet. 2013 Mar;132(3):245-63. doi: 10.1007/s00439-012-1257-0. Epub 2012 Dec 15.

Abstract

Transmission ratio distortion (TRD) occurs when one of the two alleles from either parent is preferentially transmitted to the offspring. This leads to a statistical departure from the Mendelian law of inheritance, which states that each of the two parental alleles is transmitted to offspring with a probability of 0.5. A number of mechanisms are thought to induce TRD such as meiotic drive, gametic competition, and embryo lethality. TRD has been extensively studied in animals, but the prevalence of TRD in humans remains largely unknown. Nevertheless, understanding the TRD phenomenon and taking it into consideration in many aspects of human genetics has potential benefits that have not been sufficiently emphasized in the current literature. In this review, we discuss the importance of TRD in three distinct but related fields of genetics: developmental genetics which studies the genetic abnormalities in zygotic and embryonic development, statistical genetics/genetic epidemiology which utilizes population study designs and statistical models to interpret the role of genes in human health, and population genetics which is concerned with genetic diversity in populations in an evolutionary context. From the perspective of developmental genetics, studying TRD leads to the identification of the processes and mechanisms for differential survival observed in embryos. As a result, it is a genetic force which affects allele frequency at the population, as well as, at the organismal level. Therefore, it has implications on genetic diversity of the population over time. From the perspective of genetic epidemiology, the TRD influence on a marker locus is a confounding factor which has to be adequately dealt with to correctly interpret linkage or association study results. These aspects are developed in this review. In addition to these theoretical notions, a brief summary of the empirical evidence of the TRD phenomenon in human and mouse studies is provided. The objective of our paper is to show the potentially important role of TRD in many areas of genetics, and to create an incentive for future research.

摘要

传递率失真(TRD)发生在父母双方的两个等位基因之一优先传递给后代时。这导致了与孟德尔遗传定律的统计学偏离,该定律指出,两个亲本等位基因中的每一个以 0.5 的概率传递给后代。许多机制被认为会诱导 TRD,例如减数分裂驱动、配子竞争和胚胎致死。TRD 在动物中得到了广泛的研究,但 TRD 在人类中的流行程度在很大程度上仍然未知。尽管如此,理解 TRD 现象并在人类遗传学的许多方面考虑它具有尚未在当前文献中得到充分强调的潜在益处。在这篇综述中,我们讨论了 TRD 在三个不同但相关的遗传学领域中的重要性:发育遗传学研究合子和胚胎发育中的遗传异常,统计遗传学/遗传流行病学利用群体研究设计和统计模型来解释基因在人类健康中的作用,以及群体遗传学关注进化背景下的群体遗传多样性。从发育遗传学的角度来看,研究 TRD 导致了对胚胎中观察到的差异生存过程和机制的识别。因此,它是一种影响等位基因频率的遗传力量,无论是在群体水平上,还是在个体水平上。因此,它对种群随时间的遗传多样性有影响。从遗传流行病学的角度来看,标记基因座上的 TRD 影响是一个混杂因素,必须加以适当处理,以正确解释连锁或关联研究结果。这些方面在本综述中得到了发展。除了这些理论概念外,还提供了人类和小鼠研究中 TRD 现象的实证证据的简要总结。我们的论文的目的是展示 TRD 在遗传学许多领域中的潜在重要作用,并为未来的研究创造动力。

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