Carbone M L, Solinas M, Sora S, Panzeri L
Dipartimento di Genetica e di Biologia dei Microrganismi, Università di Milano, Italy.
Curr Genet. 1991 Jan;19(1):1-8. doi: 10.1007/BF00362080.
Transcriptional analysis of the region flanking the left boundary of the centromere of chromosome VI revealed the presence of a gene immediately adjacent to CEN6. The transcription of the gene is directed toward the centromere, and nucleotide sequence analysis showed that the coding region terminates only 50 bp away from CEN6. Our results extend to chromosome VI the observation that centromere-flanking regions of S. cerevisiae are transcriptionally active. Disruption of the coding region of the gene showed that its product, whilst not essential for cell viability, is important for normal cell growth. The gene has been termed DEG1 (DEpressed Growth rate). Comparison of the deduced amino acid sequence of DEG1 with a protein sequence databank revealed homology with the enzyme tRNA pseudouridine synthase I of E. coli.
对第六条染色体着丝粒左边界侧翼区域的转录分析显示,有一个基因紧邻着丝粒CEN6。该基因的转录方向朝向着丝粒,核苷酸序列分析表明其编码区仅在距CEN6 50个碱基对处终止。我们的研究结果将酿酒酵母着丝粒侧翼区域具有转录活性这一观察结果扩展到了第六条染色体。该基因编码区的破坏表明,其产物虽然对细胞活力不是必需的,但对正常细胞生长很重要。该基因被命名为DEG1(生长速率降低基因)。将DEG1推导的氨基酸序列与蛋白质序列数据库进行比较,发现它与大肠杆菌的tRNA假尿苷合酶I具有同源性。