scholarly journals Genome-wide analysis of mono-, di- and trimethylation of histone H3 lysine 4 in Arabidopsis thaliana

2009 ◽  
Vol 10 (6) ◽  
pp. R62 ◽  
Author(s):  
Xiaoyu Zhang ◽  
Yana V Bernatavichute ◽  
Shawn Cokus ◽  
Matteo Pellegrini ◽  
Steven E Jacobsen
Author(s):  
Shaiq Sultan ◽  
Muhammad Amjid Ali ◽  
Rana Muhammad Atif ◽  
Farrukh Azeem ◽  
Habibullah Nadeem ◽  
...  

WRKY transcription factors are a class of DNA-binding proteins that bind with a specific sequence C/TTGACT/C known as W-Box found in promoters of genes which are regulated by these WRKYs. From previous studies, 43 different stress responsive WRKY transcription factors in Arabidopsis thaliana, identified and then categorized in three groups viz., abiotic, biotic and both of these stresses. A comprehensive genome wide analysis including chromosomal localization, gene structure analysis, multiple sequence alignment, phylogenetic analysis and promoter analysis of these WRKY genes was carried out in this study to determine the functional homology in Arabidopsis. This analysis led to the classification of these WRKY family members into 3 major groups and subgroups and showed evolutionary relationship among these groups on the base of their functional WRKY domain, chromosomal localization and intron/exon structure. The proposed groups of these stress responsive WRKY genes and annotation based on their position on chromosomes can also be explored to determine their functional homology in other plant species in relation to different stresses. The result of the present study provides indispensable genomic information for the stress responsive WRKY transcription factors in Arabidopsis and will pave the way to explain the precise role of various AtWRKYs in plant growth and development under stressed conditions.


2012 ◽  
Vol 22 (7) ◽  
pp. 1306-1315 ◽  
Author(s):  
E. J. Belfield ◽  
X. Gan ◽  
A. Mithani ◽  
C. Brown ◽  
C. Jiang ◽  
...  

2012 ◽  
Vol 109 (14) ◽  
pp. 5370-5375 ◽  
Author(s):  
H. Stroud ◽  
S. Otero ◽  
B. Desvoyes ◽  
E. Ramirez-Parra ◽  
S. E. Jacobsen ◽  
...  

2010 ◽  
Vol 10 (1) ◽  
pp. 238 ◽  
Author(s):  
Karin van Dijk ◽  
Yong Ding ◽  
Sridhar Malkaram ◽  
Jean-Jack M Riethoven ◽  
Rong Liu ◽  
...  

2007 ◽  
Vol 19 (11) ◽  
pp. 3418-3436 ◽  
Author(s):  
Reena Narsai ◽  
Katharine A. Howell ◽  
A. Harvey Millar ◽  
Nicholas O'Toole ◽  
Ian Small ◽  
...  

2017 ◽  
Author(s):  
Joo-Young Kang ◽  
Ji-Young Kim ◽  
Kee-Beom Kim ◽  
Jin Woo Park ◽  
Hana Cho ◽  
...  

AbstractThe methylation of histone H3 lysine 79 (H3K79) is an active chromatin marker and is prominant in actively transcribed regions of the genome. However, demethylase of H3K79 remains unknown despite intensive research. Here, we show that KDM2B (also known as FBXL10), a member of the Jumonji C family of proteins and known for its histone H3K36 demethylase activity, is a di- and tri-methyl H3K79 demethylase. We demonstrate that KDM2B induces transcriptional repression of HOXA7 and MEIS1 via occupancy of promoters and demethylation of H3K79. Furthermore, genome-wide analysis suggests that H3K79 methylation levels increase when KDM2B is depleted, indicating that KDM2B functions as an H3K79 demethylase in vivo. Finally, stable KDM2B-knockdown cell lines exhibit displacement of NAD+-dependent deacetylase SIRT1 from chromatin, with concomitant increases in H3K79 methylation and H4K16 acetylation. Our findings identify KDM2B as an H3K79 demethylase and link its function to transcriptional repression via SIRT1-mediated chromatin silencing.


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