scholarly journals Regulation of zygotic gene activation by chromatin structure and epigenetic factors

2017 ◽  
Vol 63 (4) ◽  
pp. 359-363 ◽  
Author(s):  
Satoshi FUNAYA ◽  
Fugaku AOKI
Keyword(s):  
Chromatin Structure ◽  
Gene Activation ◽  
Epigenetic Factors ◽  
Zygotic Gene ◽  
Zygotic Gene Activation

Involvement of chromatin structure in the regulation of mouse zygotic gene activation

2002 ◽  
Vol 73 (2) ◽  
pp. 113-122 ◽  
Author(s):  
Tasuku CHO ◽  
Senkiti SAKAI ◽  
Masao NAGATA ◽  
Fugaku AOKI
Keyword(s):  
Chromatin Structure ◽  
Gene Activation ◽  
Zygotic Gene ◽  
Zygotic Gene Activation

scholarly journals Minor zygotic gene activation is essential for mouse preimplantation development

2018 ◽  
Vol 115 (29) ◽  
pp. E6780-E6788 ◽  
Author(s):  
Ken-ichiro Abe ◽  
Satoshi Funaya ◽  
Dai Tsukioka ◽  
Machika Kawamura ◽  
Yutaka Suzuki ◽  
...  
Keyword(s):  
Dna Replication ◽  
Gene Activation ◽  
Marked Change ◽  
Cell Stage ◽  
Maternal Mrna ◽  
Maternal To Zygotic Transition ◽  
Before And After ◽  
H3k4me3 Mark ◽  
Zygotic Gene ◽  
Zygotic Gene Activation

In mice, transcription initiates at the mid-one-cell stage and transcriptional activity dramatically increases during the two-cell stage, a process called zygotic gene activation (ZGA). Associated with ZGA is a marked change in the pattern of gene expression that occurs after the second round of DNA replication. To distinguish ZGA before and after the second-round DNA replication, the former and latter are called minor and major ZGA, respectively. Although major ZGA are required for development beyond the two-cell stage, the function of minor ZGA is not well understood. Transiently inhibiting minor ZGA with 5, 6-dichloro-1-β-d-ribofuranosyl-benzimidazole (DRB) resulted in the majority of embryos arresting at the two-cell stage and retention of the H3K4me3 mark that normally decreases. After release from DRB, at which time major ZGA normally occurred, transcription initiated with characteristics of minor ZGA but not major ZGA, although degradation of maternal mRNA normally occurred. Thus, ZGA occurs sequentially starting with minor ZGA that is critical for the maternal-to-zygotic transition.

scholarly journals Minor Splicing Factors Zrsr1 and Zrsr2 Are Essential for Early Embryo Development and 2-Cell-Like Conversion

2020 ◽  
Vol 21 (11) ◽  
pp. 4115 ◽  
Author(s):  
Isabel Gómez-Redondo ◽  
Priscila Ramos-Ibeas ◽  
Eva Pericuesta ◽  
Raúl Fernández-González ◽  
Ricardo Laguna-Barraza ◽  
...  
Keyword(s):  
Stem Cells ◽  
Alternative Splicing ◽  
Induced Pluripotent Stem Cells ◽  
Pluripotent Stem Cells ◽  
Gene Activation ◽  
Early Embryo ◽  
Early Embryo Development ◽  
Zygotic Gene ◽  
Zygotic Gene Activation ◽  
Induced Pluripotent

Minor splicing plays an important role in vertebrate development. Zrsr1 and Zrsr2 paralog genes have essential roles in alternative splicing, mainly participating in the recognition of minor (U12) introns. To further explore their roles during early embryo development, we produced Zrsr1mu and Zrsr2mu mutant mice, containing truncating mutations within the second zinc finger domain. Both homozygous mutant mice were viable with a normal lifespan. When we crossed a homozygous Zrsr2mu/mu female with Zrsr1mu/mu male, the double heterozygotes were non-viable, giving rise to embryos that stopped developing mainly between the 2- and 4-cell stages, just after zygotic gene activation. RNA-seq analysis of Zrsr1/2mu 2-cell embryos showed altered gene and isoform expression of thousands of genes enriched in gene ontology terms and biological pathways related to ribosome, RNA transport, spliceosome, and essential zygotic gene activation steps. Alternative splicing was analyzed, showing a significant increase in intron retention in both U2 and U12 intron-containing genes related to cell cycle and mitotic nuclear division. Remarkably, both Zrsr1 and Zrsr2 were required for the conversion of mouse-induced pluripotent stem cells into 2C-like cells. According to our results, Zrsr1 or Zrsr2 are necessary for ZGA and both are indispensable for the conversion of induced pluripotent stem cells into 2C-like cells.

scholarly journals Zygotic Gene Activation and Maternal Factors in Mammals

2007 ◽  
Vol 53 (4) ◽  
pp. 707-715 ◽  
Author(s):  
Naojiro MINAMI ◽  
Toru SUZUKI ◽  
Satoshi TSUKAMOTO
Keyword(s):  
Gene Activation ◽  
Maternal Factors ◽  
Zygotic Gene ◽  
Zygotic Gene Activation

scholarly journals Paternal H3K4 methylation is required for minor zygotic gene activation and early mouse embryonic development

EMBO Reports ◽  
2015 ◽  
Vol 16 (7) ◽  
pp. 803-812 ◽  
Author(s):  
Keisuke Aoshima ◽  
Erina Inoue ◽  
Hirofumi Sawa ◽  
Yuki Okada
Keyword(s):  
Embryonic Development ◽  
Gene Activation ◽  
H3k4 Methylation ◽  
Zygotic Gene ◽  
Zygotic Gene Activation ◽  
Early Mouse

scholarly journals CDK-regulated phase separation seeded by histone genes ensures precise growth and function of Histone Locus Bodies

2019 ◽  
Author(s):  
Woonyung Hur ◽  
Marco Tarzia ◽  
Victoria E. Deneke ◽  
Esteban A. Terzo ◽  
Robert J. Duronio ◽  
...  
Keyword(s):  
Phase Separation ◽  
Gene Activation ◽  
Nuclear Body ◽  
Histone Mrnas ◽  
Histone Locus Bodies ◽  
Sex Combs ◽  
Zygotic Gene ◽  
Zygotic Gene Activation ◽  
And Function ◽  
Histone Locus

SummaryMany membrane-less organelles form through liquid-liquid phase separation, but how their size is controlled and whether size is linked to function remain poorly understood. The Histone Locus Body (HLB) is an evolutionarily conserved nuclear body that regulates the transcription and processing of histone mRNAs. Here, we show that Drosophila HLBs form through phase separation of the scaffold protein multi-sex combs (Mxc). The size of HLBs is controlled in a precise and dynamic manner that is dependent on the cell cycle and zygotic gene activation. Control of HLB growth is achieved by a mechanism integrating nascent mRNAs at the histone locus, which catalyzes phase separation, and the nuclear concentration of Mxc, which is controlled by the activity of cyclin-dependent kinases. Reduced Cdk2 activity results in smaller HLBs and the appearance of nascent, misprocessed histone mRNAs. Our experiments thus identify a mechanism linking nuclear body growth and size with gene expression.

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