Imbalance between the expression dosages of X-chromosome and autosomal genes in mammalian oocytes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep14101.pdf
Reference37 articles.
1. Gurdon, J. B. & Wilmut, I. Nuclear transfer to eggs and oocytes. Cold Spring Harb Perspect Biol 3 (2011).
2. Wen, D. et al. Histone variant H3.3 is an essential maternal factor for oocyte reprogramming. Proc Natl Acad Sci USA 111, 7325–30 (2014).
3. Wu, X. et al. Zygote arrest 1 (Zar1) is a novel maternal-effect gene critical for the oocyte-to-embryo transition. Nat Genet 33, 187–91 (2003).
4. Cantone, I. & Fisher, A. G. Epigenetic programming and reprogramming during development. Nat Struct Mol Biol 20, 282–9 (2013).
5. Kageyama, S. et al. Alterations in epigenetic modifications during oocyte growth in mice. Reproduction 133, 85–94 (2007).
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1. Dynamic Spatial-temporal Expression Ratio of X Chromosome to Autosomes but Stable Dosage Compensation in Mammals;Genomics, Proteomics & Bioinformatics;2022-08
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3. Effects of the Sex Chromosome Complement, XX, XO, or XY, on the Transcriptome and Development of Mouse Oocytes During Follicular Growth;Frontiers in Genetics;2021-12-20
4. De novo DNA methyltransferases DNMT3A and DNMT3B are essential for XIST silencing for erosion of dosage compensation in pluripotent stem cells;Stem Cell Reports;2021-09
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