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Mass spectrometry analysis of the variants of histone H3 and H4 of soybean and their post-translational modifications

BACKGROUND: Histone modifications and histone variants are of importance in many biological processes. To understand the biological functions of the global dynamics of histone modifications and histone variants in higher plants, we elucidated the variants and post-translational modifications of hist...

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Autores principales: Wu, Tao, Yuan, Tiezheng, Tsai, Sau-Na, Wang, Chunmei, Sun, Sai-Ming, Lam, Hon-Ming, Ngai, Sai-Ming
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2732622/
https://www.ncbi.nlm.nih.gov/pubmed/19643030
http://dx.doi.org/10.1186/1471-2229-9-98
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author Wu, Tao
Yuan, Tiezheng
Tsai, Sau-Na
Wang, Chunmei
Sun, Sai-Ming
Lam, Hon-Ming
Ngai, Sai-Ming
author_facet Wu, Tao
Yuan, Tiezheng
Tsai, Sau-Na
Wang, Chunmei
Sun, Sai-Ming
Lam, Hon-Ming
Ngai, Sai-Ming
author_sort Wu, Tao
collection PubMed
description BACKGROUND: Histone modifications and histone variants are of importance in many biological processes. To understand the biological functions of the global dynamics of histone modifications and histone variants in higher plants, we elucidated the variants and post-translational modifications of histones in soybean, a legume plant with a much bigger genome than that of Arabidopsis thaliana. RESULTS: In soybean leaves, mono-, di- and tri-methylation at Lysine 4, Lysine 27 and Lysine 36, and acetylation at Lysine 14, 18 and 23 were detected in HISTONE H3. Lysine 27 was prone to being mono-methylated, while tri-methylation was predominant at Lysine 36. We also observed that Lysine 27 methylation and Lysine 36 methylation usually excluded each other in HISTONE H3. Although methylation at HISTONE H3 Lysine 79 was not reported in A. thaliana, mono- and di-methylated HISTONE H3 Lysine 79 were detected in soybean. Besides, acetylation at Lysine 8 and 12 of HISTONE H4 in soybean were identified. Using a combination of mass spectrometry and nano-liquid chromatography, two variants of HISTONE H3 were detected and their modifications were determined. They were different at positions of A(31)F(41)S(87)S(90 )(HISTONE variant H3.1) and T(31)Y(41)H(87)L(90 )(HISTONE variant H3.2), respectively. The methylation patterns in these two HISTONE H3 variants also exhibited differences. Lysine 4 and Lysine 36 methylation were only detected in HISTONE H3.2, suggesting that HISTONE variant H3.2 might be associated with actively transcribing genes. In addition, two variants of histone H4 (H4.1 and H4.2) were also detected, which were missing in other organisms. In the histone variant H4.1 and H4.2, the amino acid 60 was isoleucine and valine, respectively. CONCLUSION: This work revealed several distinct variants of soybean histone and their modifications that were different from A. thaliana, thus providing important biological information toward further understanding of the histone modifications and their functional significance in higher plants.
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spelling pubmed-27326222009-08-27 Mass spectrometry analysis of the variants of histone H3 and H4 of soybean and their post-translational modifications Wu, Tao Yuan, Tiezheng Tsai, Sau-Na Wang, Chunmei Sun, Sai-Ming Lam, Hon-Ming Ngai, Sai-Ming BMC Plant Biol Research Article BACKGROUND: Histone modifications and histone variants are of importance in many biological processes. To understand the biological functions of the global dynamics of histone modifications and histone variants in higher plants, we elucidated the variants and post-translational modifications of histones in soybean, a legume plant with a much bigger genome than that of Arabidopsis thaliana. RESULTS: In soybean leaves, mono-, di- and tri-methylation at Lysine 4, Lysine 27 and Lysine 36, and acetylation at Lysine 14, 18 and 23 were detected in HISTONE H3. Lysine 27 was prone to being mono-methylated, while tri-methylation was predominant at Lysine 36. We also observed that Lysine 27 methylation and Lysine 36 methylation usually excluded each other in HISTONE H3. Although methylation at HISTONE H3 Lysine 79 was not reported in A. thaliana, mono- and di-methylated HISTONE H3 Lysine 79 were detected in soybean. Besides, acetylation at Lysine 8 and 12 of HISTONE H4 in soybean were identified. Using a combination of mass spectrometry and nano-liquid chromatography, two variants of HISTONE H3 were detected and their modifications were determined. They were different at positions of A(31)F(41)S(87)S(90 )(HISTONE variant H3.1) and T(31)Y(41)H(87)L(90 )(HISTONE variant H3.2), respectively. The methylation patterns in these two HISTONE H3 variants also exhibited differences. Lysine 4 and Lysine 36 methylation were only detected in HISTONE H3.2, suggesting that HISTONE variant H3.2 might be associated with actively transcribing genes. In addition, two variants of histone H4 (H4.1 and H4.2) were also detected, which were missing in other organisms. In the histone variant H4.1 and H4.2, the amino acid 60 was isoleucine and valine, respectively. CONCLUSION: This work revealed several distinct variants of soybean histone and their modifications that were different from A. thaliana, thus providing important biological information toward further understanding of the histone modifications and their functional significance in higher plants. BioMed Central 2009-07-31 /pmc/articles/PMC2732622/ /pubmed/19643030 http://dx.doi.org/10.1186/1471-2229-9-98 Text en Copyright © 2009 Wu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wu, Tao
Yuan, Tiezheng
Tsai, Sau-Na
Wang, Chunmei
Sun, Sai-Ming
Lam, Hon-Ming
Ngai, Sai-Ming
Mass spectrometry analysis of the variants of histone H3 and H4 of soybean and their post-translational modifications
title Mass spectrometry analysis of the variants of histone H3 and H4 of soybean and their post-translational modifications
title_full Mass spectrometry analysis of the variants of histone H3 and H4 of soybean and their post-translational modifications
title_fullStr Mass spectrometry analysis of the variants of histone H3 and H4 of soybean and their post-translational modifications
title_full_unstemmed Mass spectrometry analysis of the variants of histone H3 and H4 of soybean and their post-translational modifications
title_short Mass spectrometry analysis of the variants of histone H3 and H4 of soybean and their post-translational modifications
title_sort mass spectrometry analysis of the variants of histone h3 and h4 of soybean and their post-translational modifications
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2732622/
https://www.ncbi.nlm.nih.gov/pubmed/19643030
http://dx.doi.org/10.1186/1471-2229-9-98
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