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通过混合分组分析法和全基因组测序快速鉴定生菜种子萌发突变体

Rapid identification of lettuce seed germination mutants by bulked segregant analysis and whole genome sequencing.

作者信息

Huo Heqiang, Henry Isabelle M, Coppoolse Eric R, Verhoef-Post Miriam, Schut Johan W, de Rooij Han, Vogelaar Aat, Joosen Ronny V L, Woudenberg Leo, Comai Luca, Bradford Kent J

机构信息

Seed Biotechnology Center, Department of Plant Sciences, University of California, Davis, CA, 95616, USA.

Department of Plant Biology and Genome Center, University of California, Davis, CA, 95616, USA.

出版信息

Plant J. 2016 Nov;88(3):345-360. doi: 10.1111/tpj.13267. Epub 2016 Sep 15.

Abstract

Lettuce (Lactuca sativa) seeds exhibit thermoinhibition, or failure to complete germination when imbibed at warm temperatures. Chemical mutagenesis was employed to develop lettuce lines that exhibit germination thermotolerance. Two independent thermotolerant lettuce seed mutant lines, TG01 and TG10, were generated through ethyl methanesulfonate mutagenesis. Genetic and physiological analyses indicated that these two mutations were allelic and recessive. To identify the causal gene(s), we applied bulked segregant analysis by whole genome sequencing. For each mutant, bulked DNA samples of segregating thermotolerant (mutant) seeds were sequenced and analyzed for homozygous single-nucleotide polymorphisms. Two independent candidate mutations were identified at different physical positions in the zeaxanthin epoxidase gene (ABSCISIC ACID DEFICIENT 1/ZEAXANTHIN EPOXIDASE, or ABA1/ZEP) in TG01 and TG10. The mutation in TG01 caused an amino acid replacement, whereas the mutation in TG10 resulted in alternative mRNA splicing. Endogenous abscisic acid contents were reduced in both mutants, and expression of the ABA1 gene from wild-type lettuce under its own promoter fully complemented the TG01 mutant. Conventional genetic mapping confirmed that the causal mutations were located near the ZEP/ABA1 gene, but the bulked segregant whole genome sequencing approach more efficiently identified the specific gene responsible for the phenotype.

摘要

生菜(Lactuca sativa)种子表现出热抑制现象,即在温暖温度下吸胀时无法完成萌发。采用化学诱变方法培育出表现出发芽耐热性的生菜品系。通过甲磺酸乙酯诱变产生了两个独立的耐热生菜种子突变系TG01和TG10。遗传和生理分析表明,这两个突变是等位基因且为隐性。为了鉴定因果基因,我们通过全基因组测序应用了混合分离群体分析法。对于每个突变体,对分离的耐热(突变)种子的混合DNA样本进行测序,并分析纯合单核苷酸多态性。在TG01和TG10的玉米黄质环氧化酶基因(脱落酸缺陷1/玉米黄质环氧化酶,或ABA1/ZEP)的不同物理位置鉴定出两个独立的候选突变。TG01中的突变导致氨基酸替换,而TG10中的突变导致mRNA的可变剪接。两个突变体中的内源脱落酸含量均降低,野生型生菜的ABA1基因在其自身启动子下的表达完全互补了TG01突变体。传统的遗传图谱分析证实因果突变位于ZEP/ABA1基因附近,但混合分离群体全基因组测序方法更有效地鉴定出了导致该表型的特定基因。

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