在母体到胚胎过渡期间的表观遗传重编程
Yurong Chen1,2, Luyao Wang1,2, Fucheng Guo1,2
1Key Laboratory of Organ Regeneration and Transplantation of Ministry of Education First Hospital of Jilin University Changchun China.
MedComm
|August 7, 2023
概括
表观遗传重编程对于胚胎发育至关重要,通过控制基因激活和成分降解来调节母体到胚胎的过渡 (MZT). 它的干扰可能导致发育异常和胚胎损失.
科学领域:
- 发展生物学 发展生物学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 生殖科学 生殖科学
背景情况:
- 胚胎发育依赖于从受精到早期胚胎生成的精确调节.
- 孕产妇到胚胎的过渡 (MZT) 是一个关键的窗口,涉及孕产妇因子清除和胚胎基因组激活.
- 表观遗传重编程对于编排MZT和确保正常胚胎发育至关重要.
研究的目的:
- 审查了解哺乳动物MZT期间表观遗传重编程的最新进展.
- 讨论MZT表观遗传调节背后的分子机制.
- 突出表观遗传失调在胚胎失败中的影响.
主要方法:
- 关于表观遗传学和MZT最近发现的文献综述.
- 对低投入的表观基因组分析技术的分析.
- 合成有关分子机制和胚胎发育的数据.
主要成果:
- 新的表观遗传修饰被确定为MZT期间的关键参与者.
- 表观遗传重编程极大地影响母体成分降解和胚胎基因激活.
- 表观遗传过程的失调与异常的胚胎发育和堕胎有关.
结论:
- 表观遗传重编程是哺乳动物胚胎中MZT的中央调节者.
- 了解表观遗传调节网络对于理解早期胚胎发育至关重要.
- 表观遗传因素在自然生殖和辅助生殖中都至关重要,对胚胎的生存能力有影响.
更多相关视频
08:00Defining the Program of Maternal mRNA Translation during In vitro Maturation using a Single Oocyte Reporter Assay
Published on: June 16, 2021
4.4K
10:30Zygotic Fluorescence Recovery After Photo-bleaching Analysis for Chromatin Looseness That Allows Full-term Development
Published on: June 12, 2018
7.9K
相关概念视频
Genomic Imprinting and Inheritance
34.7K
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
34.7K
Methods of Nuclear Reprogramming
1.8K
Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for...
1.8K
Somatic to iPS Cell Reprogramming
2.2K
Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012...
2.2K
Introduction to Nuclear Reprogramming
2.0K
Nuclear reprogramming is the process of switching gene expression of one cell type to that of another cell type, usually from a differentiated cell state to an undifferentiated cell state. Differentiation occurs during processes such as development and morphogenesis, tissue regeneration, and malignancy. Cells can also be artificially induced to reprogram their gene expression by techniques such as nuclear transfer, induced pluripotency, and cell fusion. Such techniques have many applications in...
2.0K
Epigenetic Regulation
3.1K
Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
X-chromosome...
3.1K
Cleavage and Blastulation
45.3K
After a large-single-celled zygote is produced via fertilization, the process of cleavage occurs while zygotes travel through the uterine tube. Cleavage is a mitotic cell division that does not result in growth. With each round of successive cell division, daughter cells get increasingly smaller.
45.3K
