Literature DB >> 24698782

SETDB1 in Early Embryos and Embryonic Stem Cells.

Yong-Kook Kang1.   

Abstract

The histone methyltransferase SETDB1 contributes to the silencing of local chromatin and the target specificity appears to be determined through various proteins that SETDB1 interacts with. This fundamental function endows SETDB1 with specialized roles in embryonic cells. Keeping the genomic and transcriptomic integrity via proviral silencing and maintaining the pluripotency by repressing the differentiation-associated genes have been demonstrated as the roles of SETDB1 in embryonic stem cells. In early developing embryos, SETDB1 exhibits characteristic nuclear mobilizations that might account for its pleiotropic roles in these rapidly changing cells as well. Early lethality of SETDB1-null embryos, along with other immunolocalization findings, suggests that SETDB1 is necessary for reprogramming and preparing the genomes of zygotes and pluripotent cells for the post-implantation developmental program.

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Year:  2014        PMID: 24698782

Source DB:  PubMed          Journal:  Curr Issues Mol Biol        ISSN: 1467-3037            Impact factor:   2.081


  15 in total

1.  Distinct functions and temporal regulation of methylated histone H3 during early embryogenesis.

Authors:  Beste Mutlu; Huei-Mei Chen; Silvia Gutnik; David H Hall; Sabine Keppler-Ross; Susan E Mango
Journal:  Development       Date:  2019-10-10       Impact factor: 6.868

2.  Assessment of difference in gene expression profile between embryos of different derivations.

Authors:  Sujin Kwon; Sangkyun Jeong; Young Sun Jeong; Jung Sun Park; Xiang-Shun Cui; Nam-Hyung Kim; Yong-Kook Kang
Journal:  Cell Reprogram       Date:  2014-12-30       Impact factor: 1.987

Review 3.  Epigenetic mechanisms of induced pluripotency.

Authors:  Marta Gładych; Anastazja Andrzejewska; Urszula Oleksiewicz; Marcos R H Estécio
Journal:  Contemp Oncol (Pozn)       Date:  2015

4.  AGO2 and SETDB1 cooperate in promoter-targeted transcriptional silencing of the androgen receptor gene.

Authors:  Sunwha Cho; Jung Sun Park; Yong-Kook Kang
Journal:  Nucleic Acids Res       Date:  2014-09-02       Impact factor: 16.971

5.  Age-associated chromatin relaxation is enhanced in Huntington's disease mice.

Authors:  Myungsun Park; Byungkuk Min; Kyuheum Jeon; Sunwha Cho; Jung Sun Park; Jisun Kim; Jeha Jeon; Jinhoi Song; Seokho Kim; Sangkyun Jeong; Hyemyung Seo; Yong-Kook Kang
Journal:  Aging (Albany NY)       Date:  2017-03-12       Impact factor: 5.682

Review 6.  SETDB-1: A Potential Epigenetic Regulator in Breast Cancer Metastasis.

Authors:  Jacob Batham; Pek Siew Lim; Sudha Rao
Journal:  Cancers (Basel)       Date:  2019-08-09       Impact factor: 6.639

Review 7.  SETDB1 in cancer: overexpression and its therapeutic implications.

Authors:  Vanessa J Lazaro-Camp; Kiarash Salari; Xiangbing Meng; Shujie Yang
Journal:  Am J Cancer Res       Date:  2021-05-15       Impact factor: 6.166

8.  Whole exome and targeted deep sequencing identify genome-wide allelic loss and frequent SETDB1 mutations in malignant pleural mesotheliomas.

Authors:  Hio Chung Kang; Hong Kwan Kim; Sharon Lee; Pedro Mendez; James Wansoo Kim; Gavitt Woodard; Jun-Hee Yoon; Kuang-Yu Jen; Li Tai Fang; Kirk Jones; David M Jablons; Il-Jin Kim
Journal:  Oncotarget       Date:  2016-02-16

9.  Maternal Setdb1 Is Required for Meiotic Progression and Preimplantation Development in Mouse.

Authors:  Jeesun Kim; Hongbo Zhao; Jiameng Dan; Soojin Kim; Swanand Hardikar; Debra Hollowell; Kevin Lin; Yue Lu; Yoko Takata; Jianjun Shen; Taiping Chen
Journal:  PLoS Genet       Date:  2016-04-12       Impact factor: 5.917

10.  Histone Methyltransferase SETDB1 Promotes the Progression of Colorectal Cancer by Inhibiting the Expression of TP53.

Authors:  Keli Chen; Fengjiao Zhang; Jie Ding; Yonghao Liang; Zetao Zhan; Yizhi Zhan; Long-Hua Chen; Yi Ding
Journal:  J Cancer       Date:  2017-09-16       Impact factor: 4.207

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