Results 131 to 140 of about 16,350 (151)
Alternative Pathway for Methyl Supply through the Coupling of SHMT1 and PEMT to Maintain Astrocytic Homeostasis in Parkinson's Disease. [PDF]
Chen YH +17 more
europepmc +1 more source
Mapping cis- and trans-regulatory target genes of human-specific deletions. [PDF]
Fair T +5 more
europepmc +1 more source
SNF5 promotes IL-1β expression via H3K4me1 in atherosclerosis induced by homocysteine
Homocysteine (Hcy) is a strong and independent risk factor of atherosclerosis. It can accelerate atherosclerosis through increased production of inflammatory factors, especially interleukin-1 β (IL-1β), while the precise mechanisms remain to be well elucidated.
Yideng Jiang +2 more
exaly +3 more sources
Identification of H3K4me1-associated proteins at mammalian enhancers [PDF]
Enhancers act to regulate cell-type-specific gene expression by facilitating the transcription of target genes. In mammalian cells, active or primed enhancers are commonly marked by monomethylation of histone H3 at lysine 4 (H3K4me1) in a cell-type-specific manner.
Chaochen Wang +2 more
exaly +5 more sources
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Is H3K4me1 at enhancers correlative or causative?
Nature Genetics, 2017H3K4me1 is enriched at active and primed enhancers. However, whether H3K4me1 controls or simply correlates with enhancer activity and function has remained unclear. Several recent reports, including two in Nature Genetics, provide major mechanistic and functional insights into the role of H3K4me1 at enhancers.
Alvaro Rada-Iglesias +1 more
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H3K4me1 recruits DNA repair proteins in plants
Abstract DNA repair proteins can be recruited by their histone reader domains to specific epigenomic features, with consequences on intragenomic mutation rate variation. Here, we investigated H3K4me1-associated hypomutation in plants.
Gosuke Hayashi +2 more
exaly +4 more sources
Enhancer regulation by H3K4me1 methyltransferases MLL3/MLL4
The FASEB Journal, 2022Enhancers control cell type‐specific gene expression and are marked by H3K4me1. Active enhancers are further marked by H3K27ac. We identified MLL3/MLL4 as major H3K4me1 methyltransferases and CBP/p300 as the H3K27 acetyltransferases in mammalian cells ( EMBO J 2011; eLife 2013 ).
openaire +1 more source
Histone H3 lysine 4 mono-methylation (H3K4me1) marks poised or active enhancers. KMT2C (MLL3) and KMT2D (MLL4) catalyze H3K4me1, but their histone methyltransferase activities are largely dispensable for transcription during early embryogenesis in mammals.
Hiroyuki Sasaki, Bing Ren, Naoki Kubo
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Histone acetylation, including acetylated H3K14 (H3K14ac), is generally linked to gene activation. Monomethylated histone H3 lysine 4 (H3K4me1), together with other gene-activating marks, denotes active genes. In contrast to usual gene-activating functions of H3K14ac and H3K4me1, we here show that the dual histone modification mark H3K4me1-H3K14ac is ...
Jie Lv, Xiaobing Shi, Haitao Li
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