耳蜗内毛细胞对声音的感知
中文名称
通路描述
耳蜗内毛细胞(IHCs)将声波转化为离子电流(主要是钾离子),导致内毛细胞释放谷氨酸,并激活径向神经节(径向神经节)的I型突触后纤维(综述:Meyer和Moser 2010,Moser和Vogl 2016,Fettiplace 2017)。内毛细胞具有位于顶表面的纤毛,呈高度递增的“阶梯”排列。不同行纤毛之间通过由CDH23二聚体(位于较高纤毛)和PCDH15二聚体(位于较低纤毛)组成的顶链连接。PCDH15与LHFPL5(机械电转导通道MET通道,也称为机械转导通道,至少包含TMC1(成人)或TMC2(新生儿))、TMIE以及辅助亚基LHFPL5和CIB2相互作用(综述:Fettiplace和Kim 2014,Fettiplace 2016)。声波引起的纤毛偏转在顶链上产生张力,增加MET通道的开放概率,从而将钙和钾离子从 scala media 转运到内毛细胞中,导致内毛细胞去极化(综述:Fettiplace 2017)。位于细胞颈部的KCNQ4钾通道也可能参与去极化。内毛细胞的去极化打开位于内毛细胞基底侧靠近突触带的条纹区电压门控Cav1.3通道(CACNA1D:CACA2D2:CACNB2)。钙离子引起的局部钙离子 influx 通过内毛细胞中谷氨酸负载囊泡上的Otoferlin(OTOF)与钙离子的相互作用,激活谷氨酸的胞吐作用(综述:Wichmann 2015)。突触带由多蛋白复合物“突触带”表征,包含至少BASSOON、RIBEYE(CTBP2的一个等位基因)和PICCOLINO(PICCOLO的一个小等位基因),似乎通过暂时锚定囊泡靠近突触来增加易释放囊泡池(综述:Safieddine等人 2012,Wichman和Moser 2015,Pangrsic和Vogl 2018,Moser等人 2020)。ATP2B1钙通道、ATP2B2钙通道、KCNMA1:KCNMB1:LRRC52钾通道和基底侧KCNQ4钾通道将阳离子转运出内毛细胞,从而将细胞去极化并限制突触电位的持续时间(综述:Patuzzi 2011,Oak和Yi 2014)。
英文描述
RNA Polymerase II Transcription Elongation The mechanisms governing the process of elongation during eukaryotic mRNA synthesis are being unraveled by recent studies. These studies have led to the expected discovery of a diverse collection of transcription factors that directly regulate the activities of RNA Polymerase II and unexpected discovery of roles for many elongation factors in other basic processes like DNA repair, recombination, etc. The transcription machinery and structural features of the major RNA polymerases are conserved across species. The genes active during elongation fall under different classes like, housekeeping, cell-cycle regulated, development and differentiation specific genes etc. The list of genes involved in elongation has been growing in recent times, and include: -TFIIS,DSIF, NELF, P-Tefb etc. that are involved in drug induced or sequence-dependent arrest - TFIIF, ELL, elongin, elongator etc. that are involved in increasing the catalytic rate of elongation by altering the Km and/or the Vmax of Pol II -FACT, Paf1 and other factors that are involved chromatin modification - DNA repair proteins, RNA processing and export factors, the 19S proteasome and a host of other factors like Spt5-Spt5, Paf1, and NELF complexes, FCP1P etc. (Arndt and Kane, 2003). Elongation also represents processive phase of transcription in which the activities of several mRNA processing factors are coupled to transcription through their binding to RNA polymerase (Pol II). One of the key events that enables this interaction is the differential phosphorylation of Pol II CTD. Phosphorylation pattern of CTD changes during transcription, most significantly at the beginning and during elongation process. TFIIH-dependent Ser5 phosphorylation is observed primarily at promoter regions while P-Tefb mediated Ser2 phosphorylation is seen mainly in the coding regions, during elongation. Experimental evidence suggests a dynamic association of RNA processing factors with differently modified forms of the polymerase during the transcription cycle. (Komarnitsky et al., 2000). [Komarnitsky et al 2000, Arndt & Kane 2003, Shilatifard et al 2003]
所含基因
54 个基因
AFF4
CCNH
CCNK
CCNT1
CCNT2
CDC73
CDK7
CDK9
CTDP1
CTR9
EAF1
EAF2
ELL
ERCC2
ERCC3
GTF2F1
GTF2F2
GTF2H1
GTF2H2
GTF2H3
GTF2H4
GTF2H5
IWS1
LEO1
MLLT1
MLLT3
MNAT1
NELFA
NELFB
NELFCD
NELFE
PAF1
POLR2B
POLR2C
POLR2D
POLR2E
POLR2F
POLR2G
POLR2H
POLR2I
POLR2J
POLR2K
POLR2L
RTF1
SSRP1
SUPT16H
SUPT4H1
SUPT6H
TCEA1
TCEB1
TCEB2
TCEB3
TCEB3B
WDR61