Molecular evolution of a reproductive barrier in maize and related species.

IF 3.3 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2025-05-08 DOI:10.1093/genetics/iyaf085
Elli Cryan, Garnet Phinney, Arun S Seetharam, Matthew M S Evans, Elizabeth A Kellogg, Junpeng Zhan, Blake C Meyers, Daniel J Kliebenstein, Jeffrey Ross-Ibarra
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引用次数: 0

Abstract

Three cross-incompatibility loci each control a distinct reproductive barrier in both domesticated maize (Zea mays ssp. mays) and its wild teosinte relatives. These three loci, Teosinte crossing barrier1 (Tcb1), Gametophytic factor1 (Ga1), and Ga2, each play a key role in preventing hybridization between incompatible populations and are proposed to maintain the barrier between domesticated and wild subspecies. Each locus encodes both a silk-active and a matching pollen-active pectin methylesterase (PMEs). To investigate the diversity and molecular evolution of these gametophytic factor loci, we identified existing and improved models of the responsible genes in a new genome assembly of maize line P8860 that contains active versions of all three loci. We then examined fifty-two assembled genomes from seventeen species to classify haplotype diversity and identify sites under diversifying selection during the evolution of these genes. We show that Ga2, the oldest of these three loci, was duplicated to form Ga1 at least 12 million years ago. Tcb1, the youngest locus, arose as a duplicate of Ga1 before or around the time of diversification of the Zea genus. We find evidence of positive selection during evolution of the functional genes at an active site in the pollen-expressed PME and predicted surface sites in both the silk- and pollen-expressed PMEs. The most common allele at the Ga1 locus is a conserved ga1 allele (ga1-Off), which is specific haplotype containing three full-length PME gene copies, all of which are non-coding due to conserved stop codons and are between 610 thousand and 1.5 million years old. We show that the ga1-Off allele is associated with and likely generates 24-nt siRNAs in developing pollen-producing tissue, and these siRNAs map to functional Ga1 alleles. In previously-published crosses, the ga1-Off allele was associated with reduced function of the typically dominant functional alleles for the Ga1 and Tcb1 barriers. Taken together, this seems to be an example of an allele at a reproductive barrier locus being associated with an as yet undetermined mechanism capable of silencing the reproductive barrier.

玉米及其近缘种生殖屏障的分子进化。
在两个驯化玉米(Zea mays ssp)中,三个杂交不亲和位点各自控制着不同的生殖障碍。和它的野生大刍动物亲戚。Teosinte crossing barrier1 (Tcb1)、Gametophytic factor1 (Ga1)和Ga2这三个基因座在防止不亲和群体间的杂交中发挥着关键作用,并被认为可以维持驯化亚种与野生亚种之间的屏障。每个位点都编码一个具有蛛丝活性的果胶甲基酯酶(PMEs)和一个与之匹配的具有花粉活性的果胶甲基酯酶(PMEs)。为了研究这些配子体因子位点的多样性和分子进化,我们在玉米品系P8860的一个新基因组组装中鉴定了现有的和改进的负责基因模型,该基因组组装包含所有三个位点的活性版本。然后,我们检查了来自17个物种的52个组装基因组,对单倍型多样性进行分类,并确定了这些基因在进化过程中多样化选择的位点。我们发现,这三个基因座中最古老的Ga2,至少在1200万年前被复制形成Ga1。Tcb1是最年轻的基因座,在玉米属多样化之前或前后作为Ga1的复制体出现。我们发现花粉表达的PME活性位点的功能基因在进化过程中存在正选择的证据,并预测了丝绸和花粉表达的PME的表面位点。Ga1位点上最常见的等位基因是一个保守的Ga1等位基因(Ga1 - off),这是一个包含三个全长PME基因拷贝的特异性单倍型,由于保守的终止密码子,它们都是非编码的,年龄在61万到150万年之间。我们发现Ga1 - off等位基因与发育中的产花粉组织相关,并可能产生24 nt sirna,这些sirna映射到功能性Ga1等位基因。在先前发表的杂交中,Ga1 - off等位基因与Ga1和Tcb1屏障的典型显性功能等位基因的功能降低有关。综上所述,这似乎是生殖屏障位点上的等位基因与一种尚未确定的机制有关的一个例子,这种机制能够使生殖屏障沉默。
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来源期刊
Genetics
Genetics GENETICS & HEREDITY-
CiteScore
6.90
自引率
6.10%
发文量
177
审稿时长
1.5 months
期刊介绍: GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work. While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal. The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists. GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.
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