猪SOD2基因的核心促进者及其通过DNA甲基化来调节表达
Minjun Zhao1, Zhaoqi Pang1, Chunhui Jia1
1College of Animal Science and Technology, Hebei Agricultural University, Baoding 071000, China.
Veterinary sciences
|December 31, 2025
概括
DNA甲基化影响猪胎盘氧化压力. 超氧化物脱酶2 (SOD2) 核心促进物的低甲基化增强了SOD2的表达,这对母猪的抗氧化能力至关重要.
科学领域:
- 生殖生物学 生殖生物学
- 分子遗传学 分子遗传学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
背景情况:
- 母猪胎盘中的氧化应激会对猪生产产生负面影响.
- 超氧化脱酶2 (SOD2) 对于细胞抗氧化剂防御至关重要.
- DNA甲基化对猪SOD2表达的调节作用在很大程度上是未知的.
研究的目的:
- 研究DNA甲基化对猪SOD2基因表达的影响.
- 确定猪SOD2基因的核心促进子区域和关键转录因子结合位.
主要方法:
- 识别SOD2核心促进体和转录因子结合部位.
- 用DNA甲基转移酶 (DNMT) 抑制剂治疗猪胎盘细胞.
- 使用CpG甲基转移酶M.SssI治疗来评估促进体活性.
主要成果:
- SOD2核心促进体局部存在于-275/-66 bp区域.
- 用DNMT抑制剂治疗降低了促进物甲基化和增加了SOD2表达.
- M.SssI治疗降低了SOD2促进剂活性,表明甲基化的抑制作用.
结论:
- SOD2核心促进体的低甲基化增强了基因表达,而高甲基化减少了促进体的活动.
- 基因甲基化在调节猪胎盘SOD2表达方面发挥着重要作用.
- 这项研究为了解猪繁殖中SOD2的表观遗传调节提供了基础.
相关概念视频
Epigenetic Regulation
3.7K
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...
3.7K
Epigenetic Regulation
33.4K
Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
33.4K
Master Transcription Regulators
7.6K
Master transcription regulators are regulatory proteins that are predominantly responsible for regulating the expression of multiple genes. Often these genes work in concert to drive a complex process. Activation of a master transcription regulator can lead to a cascade of transcriptional activation necessary for that outcome. These regulators can directly bind to the regulatory sequences of the various genes involved, or they can indirectly regulate transcription by binding to regulatory...
7.6K
Genomic Imprinting and Inheritance
36.7K
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...
36.7K
Histone Modification
15.8K
The histone proteins have a flexible N-terminal tail extending out from the nucleosome. These histone tails are often subjected to post-translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination. Particular combinations of these modifications form “histone codes” that influence the chromatin folding and tissue-specific gene expression.
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone...
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone...
15.8K
Pleiotropy
43.1K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
43.1K


