ERCC6 (CSB) 和 EHMT2 (G9a) 正调控 rRNA 表达
中文名称
通路描述
基因组中约一半的 rRNA 基因处于活跃表达状态,由 RNA 聚合酶 I 转录(参见 Nemeth and Langst 2008, Bartova et al. 2010, Goodfellow and Zomerdijk 2012, Grummt and Langst 2013)。根据小鼠推断,这些基因的表达受 ERCC6(也称为 Cockayne 综合征蛋白,CSB)调控,该蛋白与 rRNA 基因的 T0 终止子区域(也称为 Sal Box)结合的 TTF-I 相互作用。ERCC6 招募组蛋白甲基转移酶 EHMT2(也称为 G9a),在 rRNA 基因的编码区对组蛋白 H3 的赖氨酸 9 位进行二甲基化。二甲基化的赖氨酸被 CBX3(也称为异染色质蛋白 1gamma,HP1gamma)结合,从而增加 rRNA 基因的表达。持续的二甲基化依赖于持续的转录。CSB 突变导致 RNA 聚合酶 I 转录失调,这在 Cockayne 综合征的症状中发挥作用(参见 Hannan et al. 2013)。
英文描述
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression About half of the rRNA genes in the genome are actively expressed, being transcribed by RNA polymerase I (reviewed in Nemeth and Langst 2008, Bartova et al. 2010, Goodfellow and Zomerdijk 2012, Grummt and Langst 2013). As inferred from mouse, those genes that are expressed are activated by ERCC6 (also known as Cockayne Syndrome protein, CSB) which interacts with TTF-I bound to the T0 terminator region (also know as the Sal Box) of rRNA genes (Yuan et al. 2007, reviewed in Birch and Zomerdijk 2008, Grummt and Langst 2013). ERCC6 recruits the histone methyltransferase EHMT2 (also known as G9a) which dimethylates histone H3 at lysine-9 in the coding region of rRNA genes. The dimethylated lysine is bound by CBX3 (also known as Heterochromatic Protein-1gamma, HP1gamma) and increases expression of the rRNA gene. Continuing dimethylation depends on continuing transcription. Mutations in CSB result in dysregulation of RNA polymerase I transcription, which plays a role in the symptoms of Cockayne Syndrome (reviewed in Hannan et al. 2013).
所含基因
44 个基因
CBX3
CHD3
CHD4
EHMT2
ERCC6
GATAD2A
GATAD2B
H2AFB1
H2AFJ
H2AFV
H2AFX
H2BFS
H3F3A
HDAC1
HDAC2
HIST1H2AB
HIST1H2AC
HIST1H2AD
HIST1H2AJ
HIST1H2BA
HIST1H2BB
HIST1H2BC
HIST1H2BD
HIST1H2BH
HIST1H2BJ
HIST1H2BK
HIST1H2BL
HIST1H2BM
HIST1H2BN
HIST1H2BO
HIST1H3A
HIST1H4
HIST2H2AA3
HIST2H2AC
HIST2H2BE
HIST2H3A
HIST3H2BB
MBD3
MTA1
MTA2
MTA3
RBBP4
RBBP7
TTF1