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Development and application of specific FISH probes for karyotyping Psathyrostachys huashanica chromosomes
BACKGROUND: Psathyrostachys huashanica Keng has long been used as a genetic resource for improving wheat cultivar because of its genes mediating the resistance to various diseases (stripe rust, leaf rust, take-all, and powdery mildew) as well as its desirable agronomic traits. However, a high-resolu...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017042/ https://www.ncbi.nlm.nih.gov/pubmed/35436853 http://dx.doi.org/10.1186/s12864-022-08516-6 |
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author | Zhang, Hao Wang, Fei Zeng, Chunyan Zhu, Wei Xu, Lili Wang, Yi Zeng, Jian Fan, Xing Sha, Lina Wu, Dandan Cheng, Yiran Zhang, Haiqin Chen, Guoyue Zhou, Yonghong Kang, Houyang |
author_facet | Zhang, Hao Wang, Fei Zeng, Chunyan Zhu, Wei Xu, Lili Wang, Yi Zeng, Jian Fan, Xing Sha, Lina Wu, Dandan Cheng, Yiran Zhang, Haiqin Chen, Guoyue Zhou, Yonghong Kang, Houyang |
author_sort | Zhang, Hao |
collection | PubMed |
description | BACKGROUND: Psathyrostachys huashanica Keng has long been used as a genetic resource for improving wheat cultivar because of its genes mediating the resistance to various diseases (stripe rust, leaf rust, take-all, and powdery mildew) as well as its desirable agronomic traits. However, a high-resolution fluorescence in situ hybridization (FISH) karyotype of P. huashanica remains unavailable. RESULTS: To develop chromosome-specific FISH markers for P. huashanica, repetitive sequences, including pSc119.2, pTa535, pTa713, pAs1, (AAC)(5), (CTT)(12), pSc200, pTa71A-2, and Oligo-44 were used for a FISH analysis. The results indicated that the combination of pSc200, pTa71A-2 and Oligo-44 probes can clearly identify all Ns genomic chromosomes in the two P. huashanica germplasms. The homoeologous relationships between individual P. huashanica chromosomes and common wheat chromosomes were clarified by FISH painting. Marker validation analyses revealed that the combination of pSc200, pTa71A-2, and Oligo-44 for a FISH analysis can distinguish the P. huashanica Ns-genome chromosomes from wheat chromosomes, as well as all chromosomes (except 4Ns) from the chromosomes of diploid wheat relatives carrying St, E, V, I, P and R genomes. Additionally, the probes were applicable for discriminating between the P. huashanica Ns-genome chromosomes in all homologous groups and the corresponding chromosomes in Psathyrostachys juncea and most Leymus species containing the Ns genome. Furthermore, six wheat–P. huashanica chromosome addition lines (i.e., 2Ns, 3Ns, 4Ns, 7Ns chromosomes and chromosomal segments) were characterized using the newly developed FISH markers. Thus, these probes can rapidly and precisely detect P. huashanica alien chromosomes in the wheat background. CONCLUSIONS: The FISH karyotype established in this study lays a solid foundation for the efficient identification of P. huashanica chromosomes in wheat genetic improvement programs. |
format | Online Article Text |
id | pubmed-9017042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90170422022-04-20 Development and application of specific FISH probes for karyotyping Psathyrostachys huashanica chromosomes Zhang, Hao Wang, Fei Zeng, Chunyan Zhu, Wei Xu, Lili Wang, Yi Zeng, Jian Fan, Xing Sha, Lina Wu, Dandan Cheng, Yiran Zhang, Haiqin Chen, Guoyue Zhou, Yonghong Kang, Houyang BMC Genomics Research BACKGROUND: Psathyrostachys huashanica Keng has long been used as a genetic resource for improving wheat cultivar because of its genes mediating the resistance to various diseases (stripe rust, leaf rust, take-all, and powdery mildew) as well as its desirable agronomic traits. However, a high-resolution fluorescence in situ hybridization (FISH) karyotype of P. huashanica remains unavailable. RESULTS: To develop chromosome-specific FISH markers for P. huashanica, repetitive sequences, including pSc119.2, pTa535, pTa713, pAs1, (AAC)(5), (CTT)(12), pSc200, pTa71A-2, and Oligo-44 were used for a FISH analysis. The results indicated that the combination of pSc200, pTa71A-2 and Oligo-44 probes can clearly identify all Ns genomic chromosomes in the two P. huashanica germplasms. The homoeologous relationships between individual P. huashanica chromosomes and common wheat chromosomes were clarified by FISH painting. Marker validation analyses revealed that the combination of pSc200, pTa71A-2, and Oligo-44 for a FISH analysis can distinguish the P. huashanica Ns-genome chromosomes from wheat chromosomes, as well as all chromosomes (except 4Ns) from the chromosomes of diploid wheat relatives carrying St, E, V, I, P and R genomes. Additionally, the probes were applicable for discriminating between the P. huashanica Ns-genome chromosomes in all homologous groups and the corresponding chromosomes in Psathyrostachys juncea and most Leymus species containing the Ns genome. Furthermore, six wheat–P. huashanica chromosome addition lines (i.e., 2Ns, 3Ns, 4Ns, 7Ns chromosomes and chromosomal segments) were characterized using the newly developed FISH markers. Thus, these probes can rapidly and precisely detect P. huashanica alien chromosomes in the wheat background. CONCLUSIONS: The FISH karyotype established in this study lays a solid foundation for the efficient identification of P. huashanica chromosomes in wheat genetic improvement programs. BioMed Central 2022-04-18 /pmc/articles/PMC9017042/ /pubmed/35436853 http://dx.doi.org/10.1186/s12864-022-08516-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhang, Hao Wang, Fei Zeng, Chunyan Zhu, Wei Xu, Lili Wang, Yi Zeng, Jian Fan, Xing Sha, Lina Wu, Dandan Cheng, Yiran Zhang, Haiqin Chen, Guoyue Zhou, Yonghong Kang, Houyang Development and application of specific FISH probes for karyotyping Psathyrostachys huashanica chromosomes |
title | Development and application of specific FISH probes for karyotyping Psathyrostachys huashanica chromosomes |
title_full | Development and application of specific FISH probes for karyotyping Psathyrostachys huashanica chromosomes |
title_fullStr | Development and application of specific FISH probes for karyotyping Psathyrostachys huashanica chromosomes |
title_full_unstemmed | Development and application of specific FISH probes for karyotyping Psathyrostachys huashanica chromosomes |
title_short | Development and application of specific FISH probes for karyotyping Psathyrostachys huashanica chromosomes |
title_sort | development and application of specific fish probes for karyotyping psathyrostachys huashanica chromosomes |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017042/ https://www.ncbi.nlm.nih.gov/pubmed/35436853 http://dx.doi.org/10.1186/s12864-022-08516-6 |
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