在MAPK Hog1招募Rpd3基因组脱乙酸酶激活 osmoresponsive基因
Eulàlia De Nadal1, Meritxell Zapater, Paula M Alepuz
1Cell Signaling Unit, Departament de Ciències Experimentals i de la Salut, Universitat Pompeu Fabra, E-08003 Barcelona, Spain.
Nature
|January 23, 2004
概括
线素激活蛋白激酶 (MAPK) Hog1将Rpd3-Sin3基因素脱乙酶复合物招募到回应基因促进体中. 这种向对于酵母细胞在高度应激下通过诱导基因表达而生存至关重要.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
背景情况:
- 线素激活蛋白激酶 (MAPK) 调节细胞适应的基因表达.
- 酵母中高度激活了MAPK Hog1,协调了生存反应.
- MAPK介导的基因调节机制,包括Hog1的作用,尚未完全理解.
研究的目的:
- 为了研究MAPK Hog1诱导基因表达以响应度的机制.
- 为了确定基因素脱乙酶复合体是否参与Hog1介导的基因调节.
主要方法:
- 酵母遗传学研究缺少Rpd3-Sin3复合物的透敏感突变物.
- 在Hog1和Rpd3.3之间的体内和体外相互作用研究.
- 染色体免疫沉以评估Rpd3-Sin3复合体与基因促进体的结合.
主要成果:
- 缺乏Rpd3-Sin3基因组脱乙酶复合体的细胞对高度和受损的度基因表达有敏感性.
- Hog1与Rpd3.3进行物理交互.
- 在压力下,Hog1将Rpd3-Sin3复合体向特定的度应对基因促进体,从而导致基因素脱乙烯化,RNA聚合酶II招募和基因诱导.
结论:
- 通过MAPK Hog1将Rpd3基因组脱乙酶复合体向透反应促进体,对于在透过程中诱导基因表达至关重要.
- 这种机制对于在透应激下酵母细胞生存至关重要.
相关概念视频
Histone Modification
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 deacetylase,...
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone deacetylase,...
Hedgehog Signaling Pathway
The Hedgehog gene (Hh) was first discovered due to its control of the growth of disorganized, hair-like bristles phenotype in Drosophila, much like hedgehog spines. Hh plays a crucial role in the development of organs and the maintenance of homeostasis in both invertebrates and vertebrates. However, while Drosophila has only one Hh protein, mammals have multiple functional Hedgehog proteins - Sonic (Shh), Desert (Dhh), and Indian Hedgehog (Ihh). All of these homologous proteins have adapted to...
MAPK Signaling Cascades
Mitogen-activated protein kinase, or MAPK pathway, activates three sequential kinases to regulate cellular responses such as proliferation, differentiation, survival, and apoptosis. The canonical MAPK pathway starts with a mitogen or growth factor binding to an RTK. The activated RTKs stimulate Ras, which recruits Raf or MAP3 Kinase (MAPKKK), the first kinase of the MAPK signaling cascade. Raf further phosphorylates and activates MEK or MAP2 Kinases (MAPKK), which in turn phosphorylates MAP...
The JAK-STAT Signaling Pathway
Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as SH2...
PI3K/mTOR/AKT Signaling Pathway
The mammalian target of rapamycin (mTOR) is a serine/threonine kinase that regulates growth, proliferation, and cell survival in response to hormones, growth factors, or nutrient availability. This kinase exists in two structurally and functionally distinct forms: mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2). The first form (mTORC1) is composed of a rapamycin-sensitive Raptor and proline-rich Akt substrate, PRAS40. In contrast, mTORC2 consists of a rapamycin-insensitive companion...
cAMP-dependent Protein Kinase Pathways
Cyclic Adenosine Monophosphate (cAMP) is an essential second messenger that activates protein kinase A (PKA) and regulates various biological processes. A single epinephrine molecule binds to GPCR and activates several heterotrimeric G proteins, each stimulating multiple adenylyl cyclase, amplifying the signal, and synthesizing large numbers of cAMP molecules. Small changes in cAMP concentration affect PKA activity. The binding of four cAMP molecules induces a conformational change in PKA,...


