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“SSR41”品种的全基因组DNA多态性分析、分子标记开发及白叶鞘基因的图位克隆

Genome-Wide DNA Polymorphism Analysis and Molecular Marker Development for the Variety "SSR41" and Positional Cloning of the White Leaf Sheath Gene .

作者信息

Zhang Hui, Tang Sha, Schnable James C, He Qiang, Gao Yuanzhu, Luo Mingzhao, Jia Guanqing, Feng Baili, Zhi Hui, Diao Xianmin

机构信息

Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, China.

State Key Laboratory of Crop Stress Biology for Arid Areas, College of Agronomy, Northwest A&F University, Yangling, China.

出版信息

Front Plant Sci. 2021 Nov 11;12:743782. doi: 10.3389/fpls.2021.743782. eCollection 2021.

DOI:10.3389/fpls.2021.743782
PMID:34858451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8632227/
Abstract

Genome-wide DNA polymorphism analysis and molecular marker development are important for forward genetics research and DNA marker-assisted breeding. As an ideal model system for Panicoideae grasses and an important minor crop in East Asia, foxtail millet () has a high-quality reference genome as well as large mutant libraries based on the "Yugu1" variety. However, there is still a lack of genetic and mutation mapping tools available for forward genetics research on . Here, we screened another genotype, "SSR41", which is morphologically similar to, and readily cross-pollinates with, "Yugu1". High-throughput resequencing of "SSR41" identified 1,102,064 reliable single nucleotide polymorphisms (SNPs) and 196,782 insertions/deletions (InDels) between the two genotypes, indicating that these two genotypes have high genetic diversity. Of the 8,361 high-quality InDels longer than 20 bp that were developed as molecular markers, 180 were validated with 91.5% accuracy. We used "SSR41" and these developed molecular markers to map the white leaf sheath gene . Further analyses showed that encodes a chloroplast-localized protein that is involved in the regulation of chloroplast development in bundle sheath cells in the leaf sheath in and is related to sensitivity to heavy metals. Our study provides the methodology and an important resource for forward genetics research on .

摘要

全基因组DNA多态性分析和分子标记开发对于正向遗传学研究和DNA标记辅助育种至关重要。作为黍亚科禾本科植物的理想模式系统以及东亚一种重要的小作物,谷子()拥有高质量的参考基因组以及基于“豫谷1号”品种构建的大型突变体文库。然而,仍然缺乏可用于谷子正向遗传学研究的遗传和突变定位工具。在此,我们筛选了另一个基因型“SSR41”,它在形态上与“豫谷1号”相似,并且易于与“豫谷1号”进行异花授粉。对“SSR41”进行高通量重测序,确定了这两个基因型之间有1,102,064个可靠的单核苷酸多态性(SNP)和196,782个插入/缺失(InDel),表明这两个基因型具有高度的遗传多样性。在开发为分子标记的8,361个长度超过20 bp的高质量InDel中,有180个得到验证,准确率为91.5%。我们利用“SSR41”和这些开发的分子标记对白叶鞘基因进行定位。进一步分析表明,该基因编码一种定位于叶绿体的蛋白质,参与谷子叶鞘维管束鞘细胞中叶绿体发育的调控,并且与对重金属的敏感性有关。我们的研究为谷子的正向遗传学研究提供了方法和重要资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afaf/8632227/38dd2f36c284/fpls-12-743782-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afaf/8632227/eca04d8dd719/fpls-12-743782-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afaf/8632227/6ea34ac5d15b/fpls-12-743782-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afaf/8632227/e7b77b0cc76c/fpls-12-743782-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afaf/8632227/41bda24357e0/fpls-12-743782-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afaf/8632227/e0fdece71fbb/fpls-12-743782-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afaf/8632227/38dd2f36c284/fpls-12-743782-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afaf/8632227/eca04d8dd719/fpls-12-743782-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afaf/8632227/6ea34ac5d15b/fpls-12-743782-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afaf/8632227/e7b77b0cc76c/fpls-12-743782-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afaf/8632227/41bda24357e0/fpls-12-743782-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afaf/8632227/e0fdece71fbb/fpls-12-743782-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afaf/8632227/38dd2f36c284/fpls-12-743782-g006.jpg

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