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Development of Expressed Sequence Tag-Simple Sequence Repeat Markers Related to the Salt-Stress Response of Kenaf (Hibiscus cannabinus)

文献类型： 外文期刊

作者： An, Xia 1 ; Liu, Qin 1 ; Ying, Jinyao 3 ; Wei, Jiqian 4 ; Dong, Guoyun 5 ; Luo, Xiahong 1 ; Li, Wenlue 1 ; Liu, Tingting 1 ; Zhou, Huaping 3 ; Zou, Lina 1 ; Chen, Changli 1 ;

作者机构： 1.Zhejiang Acad Agr Sci, Zhejiang Xiaoshan Inst Cotton & Bast Fiber Crops, Zhejiang Inst Landscape Plants & Flowers, Hangzhou 311251, Peoples R China

2.Yunnan Univ, Inst Resource Plants, Kunming 650500, Peoples R China

3.Hangzhou Xiaoshan Dist Agr Forestry Technol Promot, Hangzhou 311203, Peoples R China

4.Hangzhou Agr Technol Extens Ctr, Hangzhou 310020, Peoples R China

5.Zhangjiajie Res Inst Agr Sci & Technol, Zhangjiajie 427000, Peoples R China

关键词： kenaf (Hibiscus cannabinus); transcriptome sequencing; salt stress; molecular markers; EST-SSR; genetic diversity

期刊名称：AGRONOMY-BASEL （ 影响因子：3.7； 五年影响因子：4.0 ）

ISSN：

年卷期： 2023 年 13 卷 7 期

页码：

收录情况： SCI

摘要： Kenaf is one of the most important natural cannabis plants. Molecular marker-assisted breeding is vital for accelerating the breeding process of kenaf. However, the number of kenaf markers is insufficient for molecular marker-assisted breeding. Using transcriptome sequencing data for salt-stressed kenaf plants, the number and distribution of simple sequence repeats (SSRs) and single nucleotide variations (SNVs) in the expressed sequences were determined. The objectives of this study were to elucidate the sequence variations in kenaf genes expressed in response to salt stress and to identify stable and dependable molecular markers. Primers were designed for SSR loci and then EST-SSR molecular markers were generated. The subsequent analyses revealed that 30.50% of the unigenes contained SSR motifs, most of which were single nucleotides followed by trinucleotides and dinucleotides. The unigenes containing SSRs were mostly associated with kenaf salt tolerance. Additionally, 10,483 SNVs were detected in contig sequences. Of the 3995 differentially expressed genes encoding interacting proteins, 1297 contained SSRs. Most of these genes were associated with metabolic pathways (e.g., 03000 transcription factors, B09132 signal transduction, and 04122 sulfur relay system). We designed 20 pairs of EST-SSR primers to genotype 30 kenaf varieties (lines), of which 9 primer pairs were ideal for genotyping (e.g., 1 highly polymorphic marker and 2 moderately polymorphic markers). The primer pairs designed for the EST-SSR markers in the kenaf genome may be useful SSR molecular markers for future research on kenaf. The verified polymorphic markers may be applicable to the molecular marker-assisted breeding of salt-tolerant kenaf varieties.

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