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Development and comparative genomic mapping of Dasypyrum villosum 6V#4S-specific PCR markers using transcriptome data.
Theor Appl Genet. 2017 Oct; 130(10):2057-2068.TA

Abstract

KEY MESSAGE

Twenty-five Dasypyrum villosum 6V#4S-specific PCR markers were developed using transcriptome data and further assigned to comparative genomic maps of wheat chromosome 6A, 6B, and 6D and barley chromosome 6H contrasting their homologous genes in these genomes. Two Dasypyrum villosum accessions, D.v#2 and No. 1026 from England and Russia, respectively, contain Pm21 on chromosome 6V#2S and PmV on chromosome 6V#4S. Both genes confer high resistance to powdery mildew (PM) in wheat. Even though several molecular markers have been developed to detect Pm21 and PmV, only the MBH1 marker can simultaneously detect both Pm21 and PmV. In this study, we first used a high-throughput sequencing technique to obtain the transcriptome sequences of a wheat-D. villosum translocation line, Pm97033-which contains chromosome 6V#4S carrying the PmV locus, under wheat PM pathogen induction. Twenty-five 6V#4S chromosome-specific markers were developed. Three of them were able to clearly distinguish chromosomes 6V#4S and 6V#2S by product size, four amplified the product specific for chromosome 6V#4S only, and the remaining 18 markers identified chromosome 6VS in wheat backgrounds. Two different D. villosum accessions, their derived translocation lines and wheat varieties carrying different chromosome 6VS were identified using these specific markers. The 25 newly developed markers together with the known PM resistance gene Stpk-V were used to construct comparative genomic maps with the homoeologous chromosome arms of wheat and barley. The colinearity of the identified gene sequences amplified by the 25 markers among wheat chromosomes 6A, 6B, and 6D and barley chromosome 6H was not very conserved and interrupted frequently by inversion and insertion. Our markers have potential in marker assisted selection for PM resistance breeding, and for locating other potential important genes and cloning the PmV gene on chromosome 6V#4S.

Authors+Show Affiliations

Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, 100081, People's Republic of China.Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, 100081, People's Republic of China.Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, 100081, People's Republic of China.Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, 100081, People's Republic of China.Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, 100081, People's Republic of China.Institute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, 100081, People's Republic of China. yexingguo@caas.cn.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

28653149

Citation

Li, Shijin, et al. "Development and Comparative Genomic Mapping of Dasypyrum Villosum 6V#4S-specific PCR Markers Using Transcriptome Data." TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik, vol. 130, no. 10, 2017, pp. 2057-2068.
Li S, Lin Z, Liu C, et al. Development and comparative genomic mapping of Dasypyrum villosum 6V#4S-specific PCR markers using transcriptome data. Theor Appl Genet. 2017;130(10):2057-2068.
Li, S., Lin, Z., Liu, C., Wang, K., Du, L., & Ye, X. (2017). Development and comparative genomic mapping of Dasypyrum villosum 6V#4S-specific PCR markers using transcriptome data. TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik, 130(10), 2057-2068. https://doi.org/10.1007/s00122-017-2942-0
Li S, et al. Development and Comparative Genomic Mapping of Dasypyrum Villosum 6V#4S-specific PCR Markers Using Transcriptome Data. Theor Appl Genet. 2017;130(10):2057-2068. PubMed PMID: 28653149.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Development and comparative genomic mapping of Dasypyrum villosum 6V#4S-specific PCR markers using transcriptome data. AU - Li,Shijin, AU - Lin,Zhishan, AU - Liu,Chang, AU - Wang,Ke, AU - Du,Lipu, AU - Ye,Xingguo, Y1 - 2017/06/26/ PY - 2017/04/26/received PY - 2017/06/20/accepted PY - 2017/6/28/pubmed PY - 2017/11/29/medline PY - 2017/6/28/entrez SP - 2057 EP - 2068 JF - TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik JO - Theor Appl Genet VL - 130 IS - 10 N2 - KEY MESSAGE: Twenty-five Dasypyrum villosum 6V#4S-specific PCR markers were developed using transcriptome data and further assigned to comparative genomic maps of wheat chromosome 6A, 6B, and 6D and barley chromosome 6H contrasting their homologous genes in these genomes. Two Dasypyrum villosum accessions, D.v#2 and No. 1026 from England and Russia, respectively, contain Pm21 on chromosome 6V#2S and PmV on chromosome 6V#4S. Both genes confer high resistance to powdery mildew (PM) in wheat. Even though several molecular markers have been developed to detect Pm21 and PmV, only the MBH1 marker can simultaneously detect both Pm21 and PmV. In this study, we first used a high-throughput sequencing technique to obtain the transcriptome sequences of a wheat-D. villosum translocation line, Pm97033-which contains chromosome 6V#4S carrying the PmV locus, under wheat PM pathogen induction. Twenty-five 6V#4S chromosome-specific markers were developed. Three of them were able to clearly distinguish chromosomes 6V#4S and 6V#2S by product size, four amplified the product specific for chromosome 6V#4S only, and the remaining 18 markers identified chromosome 6VS in wheat backgrounds. Two different D. villosum accessions, their derived translocation lines and wheat varieties carrying different chromosome 6VS were identified using these specific markers. The 25 newly developed markers together with the known PM resistance gene Stpk-V were used to construct comparative genomic maps with the homoeologous chromosome arms of wheat and barley. The colinearity of the identified gene sequences amplified by the 25 markers among wheat chromosomes 6A, 6B, and 6D and barley chromosome 6H was not very conserved and interrupted frequently by inversion and insertion. Our markers have potential in marker assisted selection for PM resistance breeding, and for locating other potential important genes and cloning the PmV gene on chromosome 6V#4S. SN - 1432-2242 UR - https://www.unboundmedicine.com/medline/citation/28653149/Development_and_comparative_genomic_mapping_of_Dasypyrum_villosum_6V L2 - https://dx.doi.org/10.1007/s00122-017-2942-0 DB - PRIME DP - Unbound Medicine ER -