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贝壳杉烯合成酶是赤霉素生物合成中的一种关键酶,其突变赋予大白菜(Brassica rapa L. ssp. pekinensis)不结球表型。

The mutation of ent-kaurene synthase, a key enzyme involved in gibberellin biosynthesis, confers a non-heading phenotype to Chinese cabbage (Brassica rapa L. ssp. pekinensis).

作者信息

Gao Yue, Huang Shengnan, Qu Gaoyang, Fu Wei, Zhang Meidi, Liu Zhiyong, Feng Hui

机构信息

Liaoning Key Laboratory of Genetics and Breeding for Cruciferous Vegetable Crops, College of Horticulture, Shenyang Agricultural University, 110866, Shenyang, China.

出版信息

Hortic Res. 2020 Nov 1;7(1):178. doi: 10.1038/s41438-020-00399-6.

Abstract

The presence of a leafy head is a vital agronomic trait that facilitates the evaluation of the yield and quality of Chinese cabbage. A non-heading mutant (nhm1) was identified in an ethyl methanesulfonate mutagenesis population of the heading Chinese cabbage double haploid line FT. Segregation analysis revealed that a single recessive gene, Brnhm1, controlled the mutant phenotype. Using MutMap, Kompetitive allele-specific PCR, and cloning analyses, we demonstrated that BraA07g042410.3C, which encodes an ent-kaurene synthase involved in the gibberellin biosynthesis pathway, is the nhm1 mutant candidate gene. A single-nucleotide mutation (C to T) in the fourth exon of BraA07g042410.3C caused an amino acid substitution from histidine to tyrosine. Compared to that of the wild-type FT, BraA07g042410.3C in the leaves of the nhm1 mutant had lower levels of expression. In addition, gibberellin contents were lower in the mutant than in the wild type, and the mutant plant phenotype could be restored to that of the wild type after exogenous GA treatment. These results indicate that BraA07g042410.3C caused the non-heading mutation. This is the first study to demonstrate a relationship between gibberellin content in the leaves and leafy head formation in Chinese cabbage. These findings facilitate the understanding of the mechanisms underlying leafy head development in Chinese cabbage.

摘要

结球是大白菜产量和品质评估的重要农艺性状。在大白菜双单倍体系FT的甲基磺酸乙酯诱变群体中鉴定出一个不结球突变体(nhm1)。遗传分析表明,单个隐性基因Brnhm1控制该突变体表型。通过MutMap、竞争性等位基因特异性PCR和克隆分析,我们证明了BraA07g042410.3C是nhm1突变候选基因,它编码赤霉素生物合成途径中的内贝壳杉烯合酶。BraA07g042410.3C第四外显子中的单核苷酸突变(C到T)导致氨基酸从组氨酸替换为酪氨酸。与野生型FT相比,nhm1突变体叶片中的BraA07g042410.3C表达水平较低。此外,突变体中的赤霉素含量低于野生型,外源GA处理后突变体植株表型可恢复为野生型。这些结果表明BraA07g042410.3C导致了不结球突变。这是首次证明大白菜叶片中赤霉素含量与结球形成之间关系的研究。这些发现有助于理解大白菜结球发育的潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8156/7603516/4c6dcb03b3e7/41438_2020_399_Fig1_HTML.jpg

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