tRNA 修饰:细胞核和细胞质
中文名称
通路描述
在细胞核和细胞质中发现了至少 92 种不同的 tRNA 核苷酸碱基修饰。这些修饰是由位于细胞核、细胞质和线粒体中的大量不同酶共同进行的转录后修饰(综述:Boschi-Muller 和 Motorin 2013, Jackman 和 Alfonzo 2013, Gu 等 2014, Helm 和 Alfonzo 2014, Li 和 Mason 2014)。修饰靠近反密码子和 3' 端的区域分别影响 tRNA 与核糖体及 tRNA 合成酶的相互作用,而其他区域的修饰则影响 tRNA 的折叠和稳定性(综述:Hou 等 2015)。tRNA 修饰酶的突变与人类疾病相关(综述:Sarin 和 Leidel 2014, Torres 等 2014)。
英文描述
Defective B3GALT6 causes EDSP2 and SEMDJL1 The biosynthesis of dermatan sulfate/chondroitin sulfate and heparin/heparan sulfate glycosaminoglycans (GAGs) starts with the formation of a tetrasaccharide linker sequence attached to the core protein. Beta-1,3-galactosyltransferase 6 (B3GALT6) is one of the critical enzymes involved in the formation of this linker sequence. Defects in B3GALT6 causes Ehlers-Danlos syndrome progeroid type 2 (EDSP2; MIM:615349), a severe disorder resulting in a broad spectrum of skeletal, connective tissue and wound healing problems. Defects in B3GALT6 can also cause spondyloepimetaphyseal dysplasia with joint laxity type 1 (SEMDJL1; MIM:271640), characterised by spinal deformaty and lax joints, especially of the hands and respiratory compromise resulting in early death (Nakajima et al. 2013, Malfait et al. 2013).
所含基因
6 个基因