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Cloning and Regulation of Schizosaccharomyces pombe Gene Encoding Ribosomal Protein L11
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  • Cloning and Regulation of Schizosaccharomyces pombe Gene Encoding Ribosomal Protein L11
저자명
Kim. Hong-Gyum,Lee. Jin-Joo,Park. Eun-Hee,Sa. Jae-Hoon,Ahn. Ki-Sup,Lim. Chang-Jin
간행물명
Journal of biochemistry and molecular biology
권/호정보
2001년|34권 4호|pp.379-384 (6 pages)
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생화학분자생물학회
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

The cDNA encoding ribosomal protein was identified from a cDNA library of Schizosaccharomyces pombe. The nucleotide sequence of the 548 by cDNA clone reveals an open reading frame, which encodes a putative protein of 166 amino acids with a molecular mass of 18.3 kDa. The amino acid sequence of the S. pombe L11 protein is highly homologous with those of rat and fruit, while it is clearly less similar to those of prokaryotic counterparts. The 1,044 by upstream sequence, and the region encoding N-terminal 7 amino acids of the genomic DNA were fused into the promoterless $eta$-galactosidase gene of the shuttle vector YEp357 in order to generate the fusion plasmid pHY L11. Synthesis of $eta$-galactosidase from the fusion plasmid varied according to the growth curve. It decreased significantly in the growth-arrested yeast cells that were treated with aluminum chloride and mercuric chloride. However, it was enhanced by treatments with cadmium chloride ($2.5;{mu}M$), zinc chloride ($2.5;{mu}M$), and hydrogen peroxide (0.5 mM). This indicates that the expression of the L,11 gene could be induced by oxidative stress.