Chen J, Patton J R
Department of Pathology, School of Medicine, University of South Carolina, Columbia, South Carolina 29208, USA.
Biochemistry. 2000 Oct 17;39(41):12723-30. doi: 10.1021/bi001109m.
A cDNA encoding mouse pseudouridine synthase 3 (mPus3p) has been cloned. The predicted protein has 34% identity with yeast pseudouridine synthase 3 (Pus3), an enzyme known to form pseudouridine at positions 38 and 39 in yeast tRNA. The cDNA is 1.7 kb, and when used as a probe on a Northern blot of total RNA from mouse tissues or cells in culture, a band at 1.8 kb was observed. The open reading frame codes for a protein of 481 amino acids with a predicted molecular mass of 55 552 Da. When mPus3p was in vitro translated and used in reactions with tRNA substrates from both yeast and humans, uridines at position 39 were modified to pseudouridine. In a tRNA substrate with a uridine at position 38 (human tRNA(Leu)), there was very slight formation of pseudouridine at that position after incubation with mPus3p.
已克隆出编码小鼠假尿苷合酶3(mPus3p)的cDNA。预测的蛋白质与酵母假尿苷合酶3(Pus3)有34%的同源性,Pus3是一种已知在酵母tRNA的第38和39位形成假尿苷的酶。该cDNA为1.7 kb,当用作小鼠组织或培养细胞总RNA的Northern印迹探针时,观察到一条1.8 kb的条带。开放阅读框编码一个481个氨基酸的蛋白质,预测分子量为55552 Da。当mPus3p在体外翻译并用于与酵母和人类的tRNA底物反应时,第39位的尿苷被修饰为假尿苷。在第38位有尿苷的tRNA底物(人tRNA(Leu))中,与mPus3p孵育后,该位置有非常少量的假尿苷形成。