Results 1 to 10 of about 16,350 (151)

H3K4me1 directs H3K36me2 and H3K36me3 deposition in land plants [PDF]

open access: yesNature Communications
Monomethylation of histone 3 lysine 4 (H3K4me1) marks enhancers in mammals. However, the function of H3K4me1 in plants remains largely unclear. Here, we present the genome-wide distribution of H3K4me1 in diverse species across evolution, revealing a ...
Jiabing Wu   +16 more
doaj   +6 more sources

CSTF2T facilitates pancreatic adenocarcinoma growth and metastasis by elevating H3K4Me1 methylation of CALB2 via ASH2L

open access: yesCancer Biology and Therapy, 2023
Pancreatic adenocarcinoma (PAAD) is a major cause of mortality related to cancer worldwide. This paper dissected the functions of the CSTF2T/ASH2L/CALB2 axis in PAAD progression.
Bo Xu
exaly   +4 more sources

H3K27me3-H3K4me1 transition at bivalent promoters instructs lineage specification in development

open access: yesCell and Bioscience, 2023
Background Bivalent genes, of which promoters are marked by both H3K4me3 (trimethylation of histone H3 on lysine 4) and H3K27me3 (trimethylation of histone H3 on lysine 27), play critical roles in development and tumorigenesis.
, Xinjie Li, Li Xinjie
exaly   +4 more sources

H3K4me1 Distribution Predicts Transcription State and Poising at Promoters [PDF]

open access: yesFrontiers in Cell and Developmental Biology, 2020
Monomethylation on lysine 4 of histone H3 (H3K4me1) is commonly associated with distal enhancers, but H3K4me1 is also present at promoter regions proximal to transcription start sites.
Bluma J Lesch, Sunhee Bae
exaly   +5 more sources

SETD7-mediated H3K4me1 activates ALDH1A3 to drive ferroptosis resistance in esophageal squamous cell carcinoma [PDF]

open access: yesCell Death and Disease
SET domain-containing 7 (SETD7, also known as KMT7 or SET7/9), a histone lysine methyltransferase (HKMT) responsible for catalyzing histone H3 lysine 4 monomethylation (H3K4me1), has emerged as a key regulator in multiple cancers. However, the biological
Yang Feng   +10 more
doaj   +4 more sources

DNA methylation regulates discrimination of enhancers from promoters through a H3K4me1-H3K4me3 seesaw mechanism [PDF]

open access: yesBMC Genomics, 2017
Background DNA methylation at promoters is largely correlated with inhibition of gene expression. However, the role of DNA methylation at enhancers is not fully understood, although a crosstalk with chromatin marks is expected.
Hossein Baharvand   +2 more
exaly   +5 more sources

EBF2 Links KMT2D‐Mediated H3K4me1 to Suppress Pancreatic Cancer Progression via Upregulating KLLN

open access: yesAdvanced Science, 2023
Mono‐methylation of histone H3 on Lys 4 (H3K4me1), which is catalyzed by histone‐lysine N‐methyltransferase 2D (KMT2D), serves as an important epigenetic regulator in transcriptional control.
Changyan Ma
exaly   +4 more sources

Retroelement-Linked H3K4me1 Histone Tags Uncover Regulatory Evolution Trends of Gene Enhancers and Feature Quickly Evolving Molecular Processes in Human Physiology

open access: yesCells, 2019
Background: Retroelements (REs) are mobile genetic elements comprising ~40% of human DNA. They can reshape expression patterns of nearby genes by providing various regulatory sequences.
Philipp Kopylov   +2 more
exaly   +3 more sources

Sequencing DNA methylation and hydroxymethylation at co-occurring chromatin features [PDF]

open access: yesNature Communications
Epigenetic modifications govern chromatin dynamics and cell state. However, current methods cannot simultaneously resolve the presence of multiple DNA modifications at co-occurring chromatin-associated features.
Rafael de Cesaris Araujo Tavares   +9 more
doaj   +2 more sources

KMT2D‐mediated H3K4me1 recruits YBX1 to facilitate triple‐negative breast cancer progression through epigenetic activation of c‐Myc

open access: yesClinical and Translational Medicine
Background Lysine methyltransferase 2D (KMT2D) mediates mono‐methylation of histone H3 lysine 4 (H3K4me1) in mammals. H3K4me1 mark is involved in establishing an active chromatin structure to promote gene transcription.
Changyan Ma, Bing Yao, Mengying Xing
exaly   +2 more sources

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