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定位与枸杞(Lycium barbarum)自交(不)亲和性相关的数量性状基因座。

Mapping quantitative trait loci associated with self-(in)compatibility in goji berries (Lycium barbarum).

机构信息

School of Biological Science and Engineering, North Minzu University, Yinchuan, 750021, China.

State Key Laboratory of Efficient Production of Forest Resources, Yinchuan, 750004, China.

出版信息

BMC Plant Biol. 2024 May 23;24(1):441. doi: 10.1186/s12870-024-05092-7.

DOI:10.1186/s12870-024-05092-7
PMID:38778301
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11112781/
Abstract

BACKGROUND

Goji (Lycium barbarum L.) is a perennial deciduous shrub widely distributed in arid and semiarid regions of Northwest China. It is highly valued for its medicinal and functional properties. Most goji varieties are naturally self-incompatible, posing challenges in breeding and cultivation. Self-incompatibility is a complex genetic trait, with ongoing debates regarding the number of self-incompatible loci. To date, no genetic mappings has been conducted for S loci or other loci related to self-incompatibility in goji.

RESULTS

We used genome resequencing to create a high-resolution map for detecting de novo single-nucleotide polymorphisms (SNP) in goji. We focused on 229 F1 individuals from self-compatible '13-19' and self-incompatible 'new 9' varieties. Subsequently, we conducted a quantitative trait locus (QTL) analysis on traits associated with self-compatibility in goji berries. The genetic map consisted of 249,327 SNPs distributed across 12 linkage groups (LGs), spanning a total distance of 1243.74 cM, with an average interval of 0.002 cM. Phenotypic data related to self-incompatibility, such as average fruit weight, fruit rate, compatibility index, and comparable compatibility index after self-pollination and geitonogamy, were collected for the years 2021-2022, as well as for an extra year representing the mean data from 2021 to 2022 (2021/22). A total of 43 significant QTL, corresponding to multiple traits were identified, accounting for more than 11% of the observed phenotypic variation. Notably, a specific QTL on chromosome 2 consistently appeared across different years, irrespective of the relationship between self-pollination and geitonogamy. Within the localization interval, 1180 genes were annotated, including Lba02g01102 (annotated as an S-RNase gene), which showed pistil-specific expression. Cloning of S-RNase genes revealed that the parents had two different S-RNase alleles, namely S1S11 and S2S8. S-genotype identification of the F1 population indicated segregation of the four S-alleles from the parents in the offspring, with the type of S-RNase gene significantly associated with self-compatibility.

CONCLUSIONS

In summary, our study provides valuable insights into the genetic mechanism underlying self-compatibility in goji berries. This highlights the importance of further positional cloning investigations and emphasizes the importance of integration of marker-assisted selection in goji breeding programs.

摘要

背景

枸杞(Lycium barbarum L.)是一种分布广泛的多年生落叶灌木,分布在中国西北干旱和半干旱地区。它因其药用和功能特性而备受重视。大多数枸杞品种是天然自交不亲和的,这给其繁殖和栽培带来了挑战。自交不亲和是一种复杂的遗传特征,关于自交不亲和的位点数量一直存在争议。迄今为止,还没有对枸杞的 S 位点或其他与自交不亲和相关的基因座进行遗传图谱构建。

结果

我们使用基因组重测序创建了一个高分辨率图谱,用于检测枸杞中的从头单核苷酸多态性(SNP)。我们专注于自交亲和品种“13-19”和自交不亲和品种“新 9”的 229 个 F1 个体。随后,我们对与枸杞浆果自交亲和相关的性状进行了数量性状位点(QTL)分析。遗传图谱由分布在 12 个连锁群(LG)上的 249327 个 SNPs 组成,总长度为 1243.74cM,平均间隔为 0.002cM。2021-2022 年收集了与自交不亲和相关的表型数据,如平均果实重量、果实率、亲和指数和自交授粉和同株异花授粉后的可比亲和指数,以及代表 2021-2022 年平均值的额外一年(2021/22)的数据。共鉴定到 43 个与多个性状相关的显著 QTL,占观察到的表型变异的 11%以上。值得注意的是,2 号染色体上的一个特定 QTL 在不同年份都存在,无论自交和同株异花授粉之间的关系如何。在定位区间内,注释了 1180 个基因,包括 Lba02g01102(注释为 S-RNase 基因),其表现出雌蕊特异性表达。S-RNase 基因的克隆表明,亲本具有两个不同的 S-RNase 等位基因,即 S1S11 和 S2S8。F1 群体的 S 基因型鉴定表明,四个 S 等位基因在后代中从亲本中分离出来,S-RNase 基因的类型与自交亲和性显著相关。

结论

综上所述,我们的研究为枸杞浆果自交亲和的遗传机制提供了有价值的见解。这凸显了进一步进行定位克隆研究的重要性,并强调了在枸杞育种计划中整合标记辅助选择的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bc/11112781/02e184e16829/12870_2024_5092_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bc/11112781/44e2b051b001/12870_2024_5092_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bc/11112781/915da3693d44/12870_2024_5092_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bc/11112781/d3044a13c152/12870_2024_5092_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bc/11112781/38a686ad8d78/12870_2024_5092_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bc/11112781/c9faf7c6b7b0/12870_2024_5092_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bc/11112781/02e184e16829/12870_2024_5092_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bc/11112781/44e2b051b001/12870_2024_5092_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bc/11112781/915da3693d44/12870_2024_5092_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bc/11112781/d3044a13c152/12870_2024_5092_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bc/11112781/38a686ad8d78/12870_2024_5092_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bc/11112781/c9faf7c6b7b0/12870_2024_5092_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21bc/11112781/02e184e16829/12870_2024_5092_Fig6_HTML.jpg

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