The polycomb group protein PCGF6 mediates germline gene silencing by recruiting histone-modifying proteins to target gene promoters
M Liu, Y Zhu, F Xing, S Liu, Y Xia, Q Jiang… - Journal of Biological …, 2020 - ASBMB
Polycomb group (PcG) proteins are essential for maintenance of lineage fidelity by
coordinating developmental gene expression programs. Polycomb group ring finger 6 …
coordinating developmental gene expression programs. Polycomb group ring finger 6 …
CNOT 6L couples the selective degradation of maternal transcripts to meiotic cell cycle progression in mouse oocyte
QQ Sha, JL Yu, JX Guo, XX Dai, JC Jiang… - The EMBO …, 2018 - embopress.org
Meiotic resumption‐coupled degradation of maternal transcripts occurs during oocyte
maturation in the absence of mRNA transcription. The CCR 4–NOT complex has been …
maturation in the absence of mRNA transcription. The CCR 4–NOT complex has been …
Roles of tumor necrosis factor-α receptor subtypes in the pathogenesis of the tristetraprolin-deficiency syndrome
E Carballo, PJ Blackshear - … Journal of the American Society of …, 2001 - ashpublications.org
Tristetraprolin (TTP) is a member of the CCCH tandem zinc-finger class of proteins. It can
bind to and destabilize mRNAs encoding tumor necrosis factor-α (TNF-α) and granulocyte …
bind to and destabilize mRNAs encoding tumor necrosis factor-α (TNF-α) and granulocyte …
Transcriptional regulation of tristetraprolin by transforming growth factor-β in human T cells
K Ogawa, F Chen, YJ Kim, Y Chen - Journal of Biological Chemistry, 2003 - ASBMB
Transforming growth factor-β (TGF-β) is a pleiotropic cytokine that plays a critical role in
modulating immune response and inflammation. We employed the Affymetrix cDNA …
modulating immune response and inflammation. We employed the Affymetrix cDNA …
Maternal KLF17 controls zygotic genome activation by acting as a messenger for RNA Pol II recruitment in mouse embryos
Y Hu, Y Wang, Y He, M Ye, J Yuan, C Ren, X Wang… - Developmental Cell, 2024 - cell.com
Initiation of timely and sufficient zygotic genome activation (ZGA) is crucial for the beginning
of life, yet our knowledge of transcription factors (TFs) contributing to ZGA remains limited …
of life, yet our knowledge of transcription factors (TFs) contributing to ZGA remains limited …
Structure/function analysis of tristetraprolin (TTP): p38 stress-activated protein kinase and lipopolysaccharide stimulation do not alter TTP function
WFC Rigby, K Roy, J Collins, S Rigby… - The Journal of …, 2005 - journals.aai.org
Tristetraprolin (TTP) is the only trans-acting factor shown to be capable of regulating AU-rich
element-dependent mRNA turnover at the level of the intact animal; however, the …
element-dependent mRNA turnover at the level of the intact animal; however, the …
Meiosis-specific ZFP541 repressor complex promotes developmental progression of meiotic prophase towards completion during mouse spermatogenesis
Y Horisawa-Takada, C Kodera, K Takemoto… - Nature …, 2021 - nature.com
During spermatogenesis, meiosis is accompanied by a robust alteration in gene expression
and chromatin status. However, it remains elusive how the meiotic transcriptional program is …
and chromatin status. However, it remains elusive how the meiotic transcriptional program is …
Biallelic variants in ZFP36L2 cause female infertility characterised by recurrent preimplantation embryo arrest
W Zheng, QQ Sha, H Hu, F Meng, Q Zhou… - Journal of Medical …, 2022 - jmg.bmj.com
Background Recurrent preimplantation embryo developmental arrest (RPEA) is the most
common cause of assisted reproductive technology treatment failure associated with …
common cause of assisted reproductive technology treatment failure associated with …
[HTML][HTML] Molecular basis of egg coat cross-linking sheds light on ZP1-associated female infertility
Mammalian fertilisation begins when sperm interacts with the egg zona pellucida (ZP),
whose ZP1 subunit is important for fertility by covalently cross-linking ZP filaments into a …
whose ZP1 subunit is important for fertility by covalently cross-linking ZP filaments into a …
Smchd1 regulates a subset of autosomal genes subject to monoallelic expression in addition to being critical for X inactivation
Background Smchd1 is an epigenetic modifier essential for X chromosome inactivation:
female embryos lacking Smchd1 fail during midgestational development. Male mice are less …
female embryos lacking Smchd1 fail during midgestational development. Male mice are less …