Genome-wide development and utilization of Simple Sequence Repeats in Chinese cabbage (Brassica rapa L. ssp. pekinensis)

With the complementation of whole-genome sequencing of Chinese cabbage, it is necessary to develop genome-wide Simple Sequence Repeat (SSR) markers and analyse their characteristics, which will bring a revolution in the molecular marker-assisted breeding of Chinese cabbage. In this study distributio...

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Main Authors: Ying Gao, Na Li, Xiaoguang Li, Yin Lu, Daling Feng, Xiaomeng Zhang, Aixia Gu, Yunjia Ge, Javaria Tabusam, Mengyang Liu, Yanhua Wang, Xueping Chen, Shuxing Shen, Shuangxia Luo, Jianjun Zhao
Format: Article
Language:English
Published: Maximum Academic Press 2022-01-01
Series:Vegetable Research
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Online Access:https://www.maxapress.com/article/doi/10.48130/VR-2022-0009
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author Ying Gao
Na Li
Xiaoguang Li
Yin Lu
Daling Feng
Xiaomeng Zhang
Aixia Gu
Yunjia Ge
Javaria Tabusam
Mengyang Liu
Yanhua Wang
Xueping Chen
Shuxing Shen
Shuangxia Luo
Jianjun Zhao
author_facet Ying Gao
Na Li
Xiaoguang Li
Yin Lu
Daling Feng
Xiaomeng Zhang
Aixia Gu
Yunjia Ge
Javaria Tabusam
Mengyang Liu
Yanhua Wang
Xueping Chen
Shuxing Shen
Shuangxia Luo
Jianjun Zhao
author_sort Ying Gao
collection DOAJ
description With the complementation of whole-genome sequencing of Chinese cabbage, it is necessary to develop genome-wide Simple Sequence Repeat (SSR) markers and analyse their characteristics, which will bring a revolution in the molecular marker-assisted breeding of Chinese cabbage. In this study distribution and characteristics of SSR loci in the genome of Chinese cabbage 'Chiifu' was analyzed. Finally, a total of 173,892 SSR markers that occurred in 10 chromosomes were identified, and Perfect Repeat Motifs (P type) which is a main form of SSR loci with a mean distance of 1.89 kb/SSR was identified. Among them, mono-, di-, and tri-nucleotide repeat motifs were equally distributed across chromosomes compared with tetra-, penta-, and hexa-nucleotide repeat motifs. The largest proportion of SSR loci consisted of mono- and dinucleotide repeat motifs, which accounted for 93.04% of the total SSR loci. A/T and AT/TA were the most abundant motifs, accounting for 97.61% and 64.05% of the mono- and dinucleotide repeats, respectively. Furthermore, 200 SSR markers were used for the amplification of 12 Chinese cabbage germplasm, in which 30 were highly polymorphic. These SSR markers were further used for the association analyses of flowering time of 190 Chinese cabbage accessions. The results revealed that 9 and 10 alleles were associated with bolting and flowering time, respectivley. The results show that development of SSR markers is feasible and useful in marker assisted selection of Chinese cabbage.
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spelling doaj-art-3e540bd82c4d4654958ed3b646aa8a332025-08-20T02:27:15ZengMaximum Academic PressVegetable Research2769-05202022-01-01211710.48130/VR-2022-0009VR-2022-0009Genome-wide development and utilization of Simple Sequence Repeats in Chinese cabbage (Brassica rapa L. ssp. pekinensis)Ying Gao0Na Li1Xiaoguang Li2Yin Lu3Daling Feng4Xiaomeng Zhang5Aixia Gu6Yunjia Ge7Javaria Tabusam8Mengyang Liu9Yanhua Wang10Xueping Chen11Shuxing Shen12Shuangxia Luo13Jianjun Zhao14State Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaState Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaInstitute of Forestry and Fruits, Xingtai Academy of Agricultural Sciences, Xingtai, Hebei 054000, ChinaState Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaState Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaState Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaState Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaState Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaState Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaState Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaState Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaState Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaState Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaState Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaState Key Laboratory of North China Crop Improvement and Regulation, Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Collaborative Innovation Center of Vegetable Industry in Hebei, College of Horticulture, Hebei Agricultural University, Baoding 071000, ChinaWith the complementation of whole-genome sequencing of Chinese cabbage, it is necessary to develop genome-wide Simple Sequence Repeat (SSR) markers and analyse their characteristics, which will bring a revolution in the molecular marker-assisted breeding of Chinese cabbage. In this study distribution and characteristics of SSR loci in the genome of Chinese cabbage 'Chiifu' was analyzed. Finally, a total of 173,892 SSR markers that occurred in 10 chromosomes were identified, and Perfect Repeat Motifs (P type) which is a main form of SSR loci with a mean distance of 1.89 kb/SSR was identified. Among them, mono-, di-, and tri-nucleotide repeat motifs were equally distributed across chromosomes compared with tetra-, penta-, and hexa-nucleotide repeat motifs. The largest proportion of SSR loci consisted of mono- and dinucleotide repeat motifs, which accounted for 93.04% of the total SSR loci. A/T and AT/TA were the most abundant motifs, accounting for 97.61% and 64.05% of the mono- and dinucleotide repeats, respectively. Furthermore, 200 SSR markers were used for the amplification of 12 Chinese cabbage germplasm, in which 30 were highly polymorphic. These SSR markers were further used for the association analyses of flowering time of 190 Chinese cabbage accessions. The results revealed that 9 and 10 alleles were associated with bolting and flowering time, respectivley. The results show that development of SSR markers is feasible and useful in marker assisted selection of Chinese cabbage.https://www.maxapress.com/article/doi/10.48130/VR-2022-0009chinese cabbagewhole genomessrmarker assisted selection
spellingShingle Ying Gao
Na Li
Xiaoguang Li
Yin Lu
Daling Feng
Xiaomeng Zhang
Aixia Gu
Yunjia Ge
Javaria Tabusam
Mengyang Liu
Yanhua Wang
Xueping Chen
Shuxing Shen
Shuangxia Luo
Jianjun Zhao
Genome-wide development and utilization of Simple Sequence Repeats in Chinese cabbage (Brassica rapa L. ssp. pekinensis)
Vegetable Research
chinese cabbage
whole genome
ssr
marker assisted selection
title Genome-wide development and utilization of Simple Sequence Repeats in Chinese cabbage (Brassica rapa L. ssp. pekinensis)
title_full Genome-wide development and utilization of Simple Sequence Repeats in Chinese cabbage (Brassica rapa L. ssp. pekinensis)
title_fullStr Genome-wide development and utilization of Simple Sequence Repeats in Chinese cabbage (Brassica rapa L. ssp. pekinensis)
title_full_unstemmed Genome-wide development and utilization of Simple Sequence Repeats in Chinese cabbage (Brassica rapa L. ssp. pekinensis)
title_short Genome-wide development and utilization of Simple Sequence Repeats in Chinese cabbage (Brassica rapa L. ssp. pekinensis)
title_sort genome wide development and utilization of simple sequence repeats in chinese cabbage brassica rapa l ssp pekinensis
topic chinese cabbage
whole genome
ssr
marker assisted selection
url https://www.maxapress.com/article/doi/10.48130/VR-2022-0009
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