八倍体草莓历史遗传增益和杂交固定的优势假说论证

IF 3.3 3区 生物学 Q2 GENETICS & HEREDITY
Genetics Pub Date : 2024-10-10 DOI:10.1093/genetics/iyae159
Mitchell J Feldmann, Dominique D A Pincot, Danelle K Seymour, Randi A Famula, Nicolás P Jiménez, Cindy M López, Glenn S Cole, Steven J Knapp
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引用次数: 0

摘要

杂交是栽培草莓(Fragaria × ananassa)驯化的催化剂,草莓是起源于 1700 年代的种间杂交品种。杂交起源之所以被发现,是因为自发杂交种的表型超越了其亲本物种的表型。这种杂交包括在二十世纪增加果实产量和其他遗传收益,从而引发了草莓生产的全球扩张。然而,杂交对杂交种在农业上取得成功的重要性一直是个谜。在这里,我们表明,在一个为提高果实产量、重量和硬度而进行长期选育的种群(加利福尼亚种群)中,改良杂交种的异质性已经消失(固定)。我们发现,产量最高的杂交种属于近交程度最高的杂交种(59-79%),这对于一个杂合度高、遗传负荷重的外交种来说似乎有悖常理。虽然发现了微弱的杂交残余,但在加利福尼亚种群中,杂交所需的亲本间等位基因频率差异和分散的有利显性等位基因几乎在全基因组范围内都有所减少。与此相反,在宽幅杂交种中,异交现象普遍且显著,尤其是在果实数量方面,这是果实产量遗传增益的重要驱动因素。我们认为,加利福尼亚种群中异质性的消失(固定化)是由于有利的显性等位基因的同源性增加,以及与选择、随机遗传漂移和选择性横扫相关的近亲繁殖造成的。尽管近亲繁殖历史悠久,但迄今报道的最高产量杂交种估计在八倍体基因组的 97,000-108,000 个基因中具有 20,370-44,280 个杂合基因,相当于整个二倍体基因组或更多。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Dominance Hypothesis Argument for Historical Genetic Gains and the Fixation of Heterosis in Octoploid Strawberry.

Heterosis was the catalyst for the domestication of cultivated strawberry (Fragaria × ananassa), an interspecific hybrid species that originated in the 1700s. The hybrid origin was discovered because the phenotypes of spontaneous hybrids transgressed those of their parent species. The transgressions included fruit yield increases and other genetic gains in the twentieth century that sparked the global expansion of strawberry production. The importance of heterosis to the agricultural success of the hybrid species, however, has remained a mystery. Here we show that heterosis has disappeared (become fixed) among improved hybrids within a population (the California population) that has been under long-term selection for increased fruit yield, weight, and firmness. We found that the highest yielding hybrids are among the most highly inbred (59-79%), which seems counterintuitive for a highly heterozygous, outbreeder carrying heavy genetic loads. Although faint remnants of heterosis were discovered, the between-parent allele frequency differences and dispersed favorable dominant alleles necessary for heterosis have decreased nearly genome-wide within the California population. Conversely, heterosis was prevalent and significant among wide hybrids, especially for fruit count, a significant driver of genetic gains for fruit yield. We attributed the disappearance (fixation) of heterosis within the California population to increased homozygosity of favorable dominant alleles and inbreeding associated with selection, random genetic drift, and selective sweeps. Despite historical inbreeding, the highest yielding hybrids reported to-date are estimated to be heterozygous for 20,370-44,280 of 97,000-108,000 genes in the octoploid genome, the equivalent of an entire diploid genome or more.

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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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