针对异色素启动的非连续的中心动机
Runze Ma1,2,3, Yan Zhang1,2, Jing Zhang1,2
1National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Nature
|July 3, 2024
概括
指蛋白ZNF512和ZNF512B通过招募基因组甲基转移酶到周心区域来启动异染色素的形成. 这些蛋白质确保了跨物种的H3K9甲基化,尽管DNA序列是可变的.
科学领域:
- 染色体生物学
- 表观遗传学
- 分子遗传学
背景情况:
- 周心异性染色素通过基因组H3K9 (H3K9) 甲基化进行表观遗传标记.
- 招募H3K9甲基转移酶并针对跨物种保存的周心异色素标记的机制仍然未知.
研究的目的:
- 确定负责向H3K9甲基化的蛋白质.
- 阐明如何在各种脊椎动物物种中建立保存的异色素标记.
主要方法:
- 研究了指蛋白ZNF512和ZNF512B的局部化和功能.
- 测试了 de novo 异染色体的形成和基因组甲基转移酶的招募.
- 分析了特定物种对周心区域的向.
主要成果:
- ZNF512和ZNF512B直接结合周心DNA并招募SUV39H1/SUV39H2以催化H3K9甲基化.
- 这些蛋白质可以在子宫外部启动新异色素的形成.
- 由于灵活的DNA结合域,来自不同物种的ZNF512和ZNF512B的目标是保存的中心区域.
结论:
- ZNF512和ZNF512B是脊椎动物周中心区域构成异色素的关键介质.
- ZNF512/ZNF512B的灵活DNA结合特性解释了在不同物种的可变环心序列上保存的H3K9甲基化标记.
相关概念视频
Heterochromatin
12.2K
The extent of chromatin compaction can be studied by staining chromatin using specific DNA binding dyes. Under the microscope, the dense-compacted regions that take up more dye are called heterochromatin. Heterochromatin is further classified into two forms – constitutive heterochromatin and facultative heterochromatin.
Constitutive heterochromatin: It is a highly compact region of chromatin that is mostly concentrated in the centromere and telomere. Unlike euchromatin, the amino acid at...
Constitutive heterochromatin: It is a highly compact region of chromatin that is mostly concentrated in the centromere and telomere. Unlike euchromatin, the amino acid at...
12.2K
Histone Variants at the Centromere
4.3K
Histone variants are the histone proteins with structural and sequence variations. These variants may be regarded as “mutant” forms that replace their canonical histone counterparts in the nucleosomes. Specific post-translational modifications on the histone variants enable further chromatin complexity and regulate tissue-specific gene expression. The most common histone variants are from histone H2A, H2B, and linker histone H1 families. However, several variants of histone H3...
4.3K
Crossing Over
4.3K
Crossing over is the exchange of genetic information between homologous chromosomes during prophase I of meiosis I. Genetic recombination gives rise to allelic diversity in the newly formed daughter cells. In humans, crossing over produces genetically distinct haploid egg and sperm cells that undergo fertilization to produce unique offspring. Before cell division starts, the germ cell’s chromosome(s) undergo duplication in the S phase of the cell cycle. As the cells enter prophase I,...
4.3K
Inheritance of Chromatin Structures
6.2K
Epigenetics is the study of inherited changes in a cell's phenotype without changing the DNA sequences. It provides a form of memory for the differential gene expression pattern to maintain cell lineage, position-effect variegation, dosage compensation, and maintenance of chromatin structures such as telomeres and centromeres. For example, the structure and location of the centromere on chromosomes are epigenetically inherited. Its functionality is not dictated or ensured by the underlying...
6.2K
Chromatin Position Affects Gene Expression
23.3K
Chromatin is the massive complex of DNA and proteins packaged inside the nucleus. The complexity of chromatin folding and how it is packaged inside the nucleus greatly influences access to genetic information. Generally, the nucleus' periphery is considered transcriptionally repressive, while the cell's interior is considered a transcriptionally active area.
Topologically Associated Domains (TADs)
The 3-dimensional positioning of chromatin in the nucleus influences the...
Topologically Associated Domains (TADs)
The 3-dimensional positioning of chromatin in the nucleus influences the...
23.3K
Spreading of Chromatin Modifications
8.2K
The histone proteins in the nucleosomes are post-translationally modified (PTM) to increase or decrease access to DNA. The commonly observed PTMs are methylation, acetylation, phosphorylation, and ubiquitination of lysine amino acids in the histone H3 tail region. These histone modifications have specific meaning for the cell. Hence, they are called "histone code". The protein complex involved in histone modification is termed as "reader-writer" complex.
Writers
The writer...
Writers
The writer...
8.2K


