Comparative analysis of histone H3K4me3 modifications between blastocysts and somatic tissues in cattle

被引:7
|
作者
Ishibashi, Mao [1 ]
Ikeda, Shuntaro [1 ]
Minami, Naojiro [1 ]
机构
[1] Kyoto Univ, Grad Sch Agr, Lab Reprod Biol, Kyoto 6068502, Japan
基金
日本学术振兴会;
关键词
DEVELOPMENTAL ORIGINS; GENE-EXPRESSION; IN-VITRO; DISEASE; HEALTH; METHYLATION; INHERITANCE; MEMORY;
D O I
10.1038/s41598-021-87683-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Epigenetic changes induced in the early developmental stages by the surrounding environment can have not only short-term but also long-term consequences throughout life. This concept constitutes the "Developmental Origins of Health and Disease" (DOHaD) hypothesis and encompasses the possibility of controlling livestock health and diseases by epigenetic regulation during early development. As a preliminary step for examining changes of epigenetic modifications in early embryos and their long-lasting effects in fully differentiated somatic tissues, we aimed to obtain high-throughput genome-wide histone H3 lysine 4 trimethylation (H3K4me3) profiles of bovine blastocysts and to compare these data with those from adult somatic tissues in order to extract common and typical features between these tissues in terms of H3K4me3 modifications. Bovine blastocysts were produced in vitro and subjected to chromatin immunoprecipitation-sequencing analysis of H3K4me3. Comparative analysis of the blastocyst-derived H3K4me3 profile with publicly available data from adult liver and muscle tissues revealed that the blastocyst profile could be used as a "sieve" to extract somatic tissue-specific modifications in genes closely related to tissue-specific functions. Furthermore, principal component analysis of the level of common modifications between blastocysts and somatic tissues in meat production-related and imprinted genes well characterized inter- and intra-tissue differences. The results of this study produced a referential genome-wide H3K4me3 profile of bovine blastocysts within the limits of their in vitro source and revealed its common and typical features in relation to the profiles of adult tissues.
引用
收藏
页数:10
相关论文
共 50 条
  • [41] Ageing-Related Changes to H3K4me3, H3K27ac, and H3K27me3 in Purified Mouse Neurons
    Signal, Brandon
    Phipps, Andrew J.
    Giles, Katherine A.
    Huskins, Shannon N.
    Mercer, Timothy R.
    Robinson, Mark D.
    Woodhouse, Adele
    Taberlay, Phillippa C.
    CELLS, 2024, 13 (16)
  • [42] Whole-genome landscape of histone H3K4me3 modification during sperm cell lineage development in tomato
    Song, Yunyun
    Chang, Zhikai
    Feng, Yixuan
    Wang, Tai
    Liu, Lingtong
    BMC PLANT BIOLOGY, 2024, 24 (01):
  • [43] Dynamic Histone Acetylation of H3K4me3 Nucleosome Regulates MCL1 Pre-mRNA Splicing
    Khan, Dilshad H.
    Gonzalez, Carolina
    Tailor, Nikesh
    Hamedani, Mohammad K.
    Leygue, Etienne
    Davie, James R.
    JOURNAL OF CELLULAR PHYSIOLOGY, 2016, 231 (10) : 2196 - 2204
  • [44] Efficient chromatin profiling of H3K4me3 modification in cotton using CUT&Tag
    Tao, Xiaoyuan
    Feng, Shouli
    Zhao, Ting
    Guan, Xueying
    PLANT METHODS, 2020, 16 (01)
  • [45] Paternal reprogramming-escape histone H3K4me3 marks located within promoters of RNA splicing genes
    Hao, Nan
    Xin, Huawei
    Shi, Xiaowei
    Xin, Jie
    Zhang, Haijuan
    Guo, Shaofen
    Wang, Zhen
    Hao, Chunxiang
    BIOINFORMATICS, 2021, 37 (08) : 1039 - 1044
  • [46] Histone demethylase PHF8 regulates hypoxia signaling through HIF1α and H3K4me3
    Maina, Peterson Kariuki
    Shao, Peng
    Jia, Xiongfei
    Liu, Qi
    Umesalma, Shaikamjad
    Marin, Maximo
    Long, Donald, Jr.
    Concepcion-Roman, Samantha
    Qi, Hank Heng
    BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS, 2017, 1860 (09): : 1002 - 1012
  • [47] Dynamic variation of histone H3 trimethyl Lys4 (H3K4me3) and heterochromatin protein 1 (HP1) with employment length in nickel smelting workers
    Zhao, Yanhong
    Cheng, Ning
    Dai, Min
    Pu, Hongquan
    Zheng, Tongzhang
    Li, Haiyan
    He, Jie
    Bai, Yana
    BIOMARKERS, 2017, 22 (05) : 420 - 428
  • [48] Dynamic and aberrant patterns of H3K4me3, H3K9me3, and H3K27me3 during early zygotic genome activation in cloned mouse embryos
    Liu, Zhihui
    Cui, Jing
    Wang, Weiguo
    Li, Mingyang
    Wang, Zhisong
    Presicce, Giorgio Antonio
    Tian, Xiuchun
    An, Liyou
    Du, Fuliang
    ZYGOTE, 2022, 30 (06) : 903 - 909
  • [49] The Role of H3K4me3 in Transcriptional Regulation Is Altered in Huntington's Disease
    Dong, Xianjun
    Tsuji, Junko
    Labadorf, Adam
    Roussos, Panos
    Chen, Jiang-Fan
    Myers, Richard H.
    Akbarian, Schahram
    Weng, Zhiping
    PLOS ONE, 2015, 10 (12):
  • [50] A central role of H3K4me3 extended chromatin domains in gene regulation
    Bayarsaihan, Dashzeveg
    EPIGENOMICS, 2016, 8 (08) : 1011 - 1014