生物多样性

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生殖隔离和物种形成基因

蒋永山, 刘建全*   

  1. 兰州大学生态学院,草种创新与草地农业生态系统全国重点实验室,兰州 730000
  • 收稿日期:2026-07-23 修回日期:2026-09-13 接受日期:2026-10-03
  • 通讯作者: 刘建全

Reproductive isolation and speciation genes

Yongshan Jiang, Jianquan Liu*   

  1. State Key Laboratory of Herbage Improvement and Grassland Agro-Ecosystems, College of Ecology, Lanzhou University, Lanzhou 730000, China
  • Received:2026-07-23 Revised:2026-09-13 Accepted:2026-10-03
  • Contact: Jianquan Liu

摘要: 生殖隔离是物种形成与维持的关键标志,但“生殖隔离基因”常被等同于“物种形成基因”。生殖隔离基因是广义集合:凡在群体间显著分化,并在生活史任一阶段降低有效种间交配后代产生的遗传元件均属之,其数量随分化时间累积。物种形成基因则是其中在谱系分化起点最早建立初始生殖隔离、启动独立演化的奠基性基因,须同时满足“参与生殖隔离”和“最早驱动分化”。近缘种间生殖隔离多不完全,由多屏障顺序作用并协同累积。二歧分化中,后期合子后生殖隔离基因可源于连锁搭车或时间累积,成为“搭车者/加固者”;受自然选择(含性选择)驱动的合子前隔离更可能启动分化。地理隔离非必要条件,但可阻断基因流并加速选择介导的分化。同倍杂交物种(包括亚种)形成(不涉及染色体倍性变化)中,物种形成基因的鉴定相对容易,得益于新机制认知及技术方法的进步。其遗传逻辑类似于种内杂交F₂代中非等位基因自由组合(如AABBCCDD与aabbccdd杂交产生AAbbCCdd基因型),但种间杂交F₂代因亲本物种间生殖隔离常致个体死亡,不呈现孟德尔表型或基因型预期比例,却会出现更为丰富的非等位基因组合及其组合表型、尤其是非等位基因新互作产生的创新性状。具有这些特殊表型的杂交个体通过迭代恢复育性与固定下来的多位点高分化组合基因,若与亲本生殖隔离相关,则可视为该过程的物种形成基因。最后,我们建议未来研究应从静态的“基因-生殖性状”关联转向动态的生殖隔离基因演化历史重构,以更好地鉴定物种形成基因;而远缘同倍杂交迭代演化则通过丰富的非等位基因重组可创制新组合表型或新性状,为农业育种提供了新途径,也为解析基因新互作等分子遗传机制提供了类似‘创制突变体’的新材料。

关键词: 不完全生殖隔离, 物种形成基因, 二歧分化, 同倍杂交物种形成, 非等位基因重组, 基因新互作

Abstract

Background & Aims: Reproductive isolation is a key hallmark of speciation and species maintenance, but "reproductive isolation genes" are often equated with "speciation genes." Reproductive isolation genes constitute a broad set: any genetic element that is significantly differentiated between populations and reduces effective interspecific progeny at any stage of the life cycle belongs to this set, and they accumulate over divergence time. Speciation genes, by contrast, are the founding genes within this set that earliest establish initial reproductive isolation at the origin of lineage divergence and initiate independent evolution, and they must simultaneously satisfy "participating in reproductive isolation" and "earliest driving divergence." 

Review Results: Reproductive isolation between closely related species is often incomplete, arising from the sequential action and synergistic accumulation of multiple barriers. In dichotomous divergence, later-stage postzygotic isolation genes may originate from linkage hitchhiking or temporal accumulation, becoming "hitchhikers/reinforcers"; prezygotic isolation driven by natural selection (including sexual selection) is more likely to initiate divergence. Geographic isolation is not a necessary condition, but it can block gene flow and accelerate selection-mediated divergence. In homoploid hybrid speciation (not involving changes in chromosome ploidy between species or subspecies), the identification of speciation genes is relatively easier, benefiting from advances in the mechanism understanding and technical methods. Its genetic logic is similar to the free assortment of non-allelic genes and traits in F₂ generations of intraspecific crosses, for example, crosses between AABBCCDD and aabbccdd to produce the genotype AAbbCCdd, but F₂ generations of interspecific (or intersubspecific) crosses often suffer individual death due to reproductive isolation, failing to exhibit Mendelian expected genotype or phenotype ratios, yet displaying extremely diverse array of recombinant and novel traits due to non-allelic recombination even totally new non-allelic gene interactions. If the multi-locus highly differentiated recombinant genes in hybrid offspring with these phenotypes that are fixed through iterative fertility restoration are associated with reproductive isolation with parents, they can be regarded as the speciation genes of this process. 

Conclusions: We suggest that future research should shift from static "gene-reproductive trait" associations to dynamic reconstruction of the evolutionary history of reproductive isolation genes, so as to better identify speciation genes; and that iterative distant homoploid hybridization through rich non-allelic recombination can create novel recombinant or novel traits, providing a new avenue for agricultural breeding and materials similar to ‘creating mutants’ for dissecting the underlying molecular genetic mechanisms, including new gene interactions and others.

Key words: Incomplete reproductive isolation, speciation genes, dichotomous divergence, homoploid hybrid speciation, non-allelic recombination, new gene interaction