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林业科学 ›› 2002, Vol. 38 ›› Issue (2): 119-128.doi: 10.11707/j.1001-7488.20020221

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群体遗传结构的理解

胡新生   

  1. 中国林业科学研究院林业研究所,北京100091
  • 收稿日期:1998-09-28 修回日期:1900-01-01 出版日期:2002-03-25 发布日期:2002-03-25

A REVIEW ON UNDERSTANDING THE GENETIC STRUCTURE OF POPULATION

Hu Xinsheng   

  1. The Research Institute of Forestry, CAF Beijing 100091
  • Received:1998-09-28 Revised:1900-01-01 Online:2002-03-25 Published:2002-03-25

摘要:

一个植物种群体的空间分布大致可划分为两类:离散分布与连续分布。然而隐藏在这种表观物理分布内部的遗传变异是十分复杂的。这种变异是如何分布的呢?这种分布又是如何维持的呢?因此,认识一个种的群体遗传结构有助于我们理解该种的进化过程,并提供为遗传资源保护做出决策的重要信息。本文对三大经典遗传结构模型(岛屿模型、步石模型及距离隔离模型)与渐变群理论及它们的异体和发展进行了详细的分析和评述。目前获得的许多不同类型的遗传标记使这些理论的应用得到不同程度的实现,但由于这些理论结论涉及到许多假设,在实际应用时应十分慎重。作者认为许多已建立的适合于动物群体遗传结构理论不能简单地直接应用于植物群体上,今后一个重要的研究内容就是要建立适合于植物群体的遗传结构理论。

关键词: 群体遗传结构, 岛屿模型, 步石模型, 距离隔离模型, 渐变群理论

Abstract:

Population distribution of a species in space can be generally classified two types: discrete and continuous distribution, but the genetic variation underlying this physical distribution is very complicated. How does the genetic variation partition between and within populations? How can this genetic variation be maintained in real world? Thus, knowledge of population genetic structure may help us to understand the evolutionary process of the species and assist us in decision-making on conservation of genetic resources. So far insight into population genetic structure is very restricted, and theoretical studies are mainly confined to the three classical models of genetic structure: island model (Wright,1931), stepping-stone model (Kimura,1953) and isolation by distance model (Wright,1943). The first two models can be used to address the case of discrete distribution in space, and the third one to the case of continuous distribution. Since the introduction of these three models, many limitations involved in them have been relaxed and their variants have been developed and analyzed using a variety of statistical genetic methods. In this paper, the three models and their variants and cline theory, a specific genetic structure of populations in terms of the change of genetic variation with geographical distance, were remarked in detail, including their kernel ideas, application limitations and relaxation, development, and testing of our understanding using the naturally occurring genetic markers within taxa. In the end, the author highlighted the requirement of exploring appropriate theory suitable for genetic structure of plant populations because there are many obvious differences between plant and animal population genetic structure. Firstly, vectors of gene flow in plant species are different from those in animals. Secondly, the migration rate contained in the formulae of traditional population structure models cannot be substituted linearly by seed and pollen flow if rates of seed and pollen flow are not too small, which is highly likely in many plant species. Thirdly, population genetic structures of three plant genomes with contrasting modes of inheritance are different. Fourthly, differences in population structure among three plant genomes can provide important information on estimation of seed and pollen flow, on inferring colonization history, etc.. The integration of the impacts of seed and pollen flow with the interaction between cytonuclear genes probably can gain deep insight into the genetic structure of natural plant populations.

Key words: Population genetic structure, Island model, Stepping-stone model, Isolation by distance model, Cline theory