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Mitochondrial transcription termination

Reactome ID: R-HSA-163316

中文名称

胆固醇从泽马司特(修改版的坎杜什 - 鲁塞尔途径)的生物合成

通路描述

完整 KR 途径在完整小鼠和人类以及小鼠细胞系中的示踪研究表明,任何组织中都没有通过该途径的流量。相反,观察到该途径的修改形式,其中 delta(24)-固醇还原酶(DHCR24)将泽马司特(ZYMOL,布洛赫途径的中间体)还原为泽马松醇(ZYMSTNL,KR 途径的中间体),然后通过 KR 途径的最后三步代谢形成胆固醇。该途径的使用在皮肤、前庭腺和大脑中被观察到(Mitsche et al. 2015)。
英文描述
Mitochondrial transcription termination Transcription of the heavy (H)-strand of mitochondrial DNA (mtDNA) involves two overlapping transcription units (Montoyaet al.,1982; Montoya et al., 1983). The first unit starts right upstream of the tRNAPhe gene and spans the tRNAPhe, rRNA 12S, rRNA 16S and tRNAVal genes (initiation site IH1). The other starts about 100 bp further downstream (initiation site IH2), at the boundary between tRNAPhe and rRNA12S genes, and produces a single polycistronic RNA that encompasses almost the entire length of the H-strand. The ribosomal transcription unit is transcribed at a much higher rate compared to the other transcription unit and control of its expression is exerted both at the level of initiation and termination (Gelfand and Attardi, 1981; Attardi et al., 1990). A central role in the control of termination has been attributed to the mitochondrial transcription termination factor (mTERF), a 39-kDa protein that binds to a 28-base pair region of mtDNA located within the tRNALeu(UUR) gene, at a position immediately downstream of the rRNA 16S gene (Fernandez-Silva et al.,1997; Kruse et al., 1989).

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