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Comprehensive analysis of the MYB transcription factor gene family in Morus alba

BACKGROUND: The V-myb myeloblastosis viral oncogene homolog (MYB) family of proteins is large, containing functionally diverse transcription factors. However, MYBs in Morus are still poorly annotated and a comprehensive functional analysis of these transcription factors is lacking. RESULTS: In the p...

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Autores principales: Liu, Li, Chao, Nan, Yidilisi, Keermula, Kang, Xiaoru, Cao, Xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175366/
https://www.ncbi.nlm.nih.gov/pubmed/35676625
http://dx.doi.org/10.1186/s12870-022-03626-5
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author Liu, Li
Chao, Nan
Yidilisi, Keermula
Kang, Xiaoru
Cao, Xu
author_facet Liu, Li
Chao, Nan
Yidilisi, Keermula
Kang, Xiaoru
Cao, Xu
author_sort Liu, Li
collection PubMed
description BACKGROUND: The V-myb myeloblastosis viral oncogene homolog (MYB) family of proteins is large, containing functionally diverse transcription factors. However, MYBs in Morus are still poorly annotated and a comprehensive functional analysis of these transcription factors is lacking. RESULTS: In the present study, a genome-wide identification of MYBs in Morus alba was performed. In total 166 MaMYBs were identified, including 103 R2R3-MYBs and four 3R-MaMYBs. Comprehensive analyses, including the phylogenetic analysis with putative functional annotation, motif and structure analysis, gene structure organization, promoter analysis, chromosomal localization, and syntenic relationships of R2R3-MaMYBs and 3R-MaMYBs, provided primary characterization for these MaMYBs. R2R3-MaMYBs covered the subgroups reported for R2R3-MYBs in Arabidopsis and Populus, and had two Morus-specific subgroups, indicating the high retention of MYBs in Morus. Motif analysis revealed high conservative residues at the start and end of each helix and residues consisting of the third helix in R2 and R3 repeats. Thirteen intron/exon patterns (a–m) were summarized, and the intron/exon pattern of two introns with phase numbers of 0 and 2 was the prevalent pattern for R2R3-MaMYBs. Various cis-elements in promoter regions were identified, and were mainly related to light response, development, phytohormone response, and abiotic and biotic stress response and secondary metabolite production. Expression patterns of R2R3-MaMYBs in different organs showed that MaMYBs involved in secondary cell wall components and stress responsiveness were preferentially expressed in roots or stems. R2R3-MaMYBs involved in flavonoid biosynthesis and anthocyanin accumulation were identified and characterized based on functional annotation and correlation of their expression levels with anthocyanin contents. CONCLUSION: Based on a comprehensive analysis, this work provided functional annotation for R2R3-MYBs and an informative reference for further functional dissection of MYBs in Morus. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-022-03626-5.
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spelling pubmed-91753662022-06-09 Comprehensive analysis of the MYB transcription factor gene family in Morus alba Liu, Li Chao, Nan Yidilisi, Keermula Kang, Xiaoru Cao, Xu BMC Plant Biol Research BACKGROUND: The V-myb myeloblastosis viral oncogene homolog (MYB) family of proteins is large, containing functionally diverse transcription factors. However, MYBs in Morus are still poorly annotated and a comprehensive functional analysis of these transcription factors is lacking. RESULTS: In the present study, a genome-wide identification of MYBs in Morus alba was performed. In total 166 MaMYBs were identified, including 103 R2R3-MYBs and four 3R-MaMYBs. Comprehensive analyses, including the phylogenetic analysis with putative functional annotation, motif and structure analysis, gene structure organization, promoter analysis, chromosomal localization, and syntenic relationships of R2R3-MaMYBs and 3R-MaMYBs, provided primary characterization for these MaMYBs. R2R3-MaMYBs covered the subgroups reported for R2R3-MYBs in Arabidopsis and Populus, and had two Morus-specific subgroups, indicating the high retention of MYBs in Morus. Motif analysis revealed high conservative residues at the start and end of each helix and residues consisting of the third helix in R2 and R3 repeats. Thirteen intron/exon patterns (a–m) were summarized, and the intron/exon pattern of two introns with phase numbers of 0 and 2 was the prevalent pattern for R2R3-MaMYBs. Various cis-elements in promoter regions were identified, and were mainly related to light response, development, phytohormone response, and abiotic and biotic stress response and secondary metabolite production. Expression patterns of R2R3-MaMYBs in different organs showed that MaMYBs involved in secondary cell wall components and stress responsiveness were preferentially expressed in roots or stems. R2R3-MaMYBs involved in flavonoid biosynthesis and anthocyanin accumulation were identified and characterized based on functional annotation and correlation of their expression levels with anthocyanin contents. CONCLUSION: Based on a comprehensive analysis, this work provided functional annotation for R2R3-MYBs and an informative reference for further functional dissection of MYBs in Morus. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12870-022-03626-5. BioMed Central 2022-06-08 /pmc/articles/PMC9175366/ /pubmed/35676625 http://dx.doi.org/10.1186/s12870-022-03626-5 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
Liu, Li
Chao, Nan
Yidilisi, Keermula
Kang, Xiaoru
Cao, Xu
Comprehensive analysis of the MYB transcription factor gene family in Morus alba
title Comprehensive analysis of the MYB transcription factor gene family in Morus alba
title_full Comprehensive analysis of the MYB transcription factor gene family in Morus alba
title_fullStr Comprehensive analysis of the MYB transcription factor gene family in Morus alba
title_full_unstemmed Comprehensive analysis of the MYB transcription factor gene family in Morus alba
title_short Comprehensive analysis of the MYB transcription factor gene family in Morus alba
title_sort comprehensive analysis of the myb transcription factor gene family in morus alba
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175366/
https://www.ncbi.nlm.nih.gov/pubmed/35676625
http://dx.doi.org/10.1186/s12870-022-03626-5
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