GENE MRP-L4, ENCODING MITOCHONDRIAL RIBOSOMAL-PROTEIN YML4, IS INDISPENSABLE FOR PROPER NON-RESPIRATORY CELL FUNCTIONS IN YEAST

被引:11
作者
GRAACK, HR
GROHMANN, L
KITAKAWA, M
GOLDSCHMIDTREISIN, S
机构
[1] INST GENBIOL FORSCH, D-14195 BERLIN, GERMANY
[2] KOBE UNIV, FAC SCI, DEPT BIOL, NADA KU, KOBE 657, JAPAN
[3] TEL AVIV UNIV, DEPT BIOCHEM, IL-69978 TEL AVIV, ISRAEL
关键词
RESPIRATORY DEFICIENCY; SIGNAL PEPTIDE; MITOCHONDRIAL IMPORT; PROTEIN BIOSYNTHESIS; SACCHAROMYCES CEREVISIAE;
D O I
10.1016/0378-1119(94)00633-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In order to characterize individual protein components of the mitochondrial (mt) ribosome for regulatory, functional and evolutionary studies, the yeast nuclear gene MRP-L4 (accession No. Z30582), coding for the mt ribosomal protein (MRP) YmL4, has been cloned using oligodeoxyribonucleotides (oligos) deduced from a partial amino acid (aa) sequence [Graack et al., FEES Lett. 242 (1988) 4-8] as screening probes. MRP-L4 is located on chromosome XII and codes for a slightly basic protein of 319 aa. The first 14 aa have not been found in the mature protein, and putatively form a signal peptide that is cleaved off during or after mt import. YmL4 has an N terminus very rich in Pro residues, and at its C terminus contains four hydrophobic domains, YmL4 shows no significant sequence similarity to any other sequence from the databases. Gene disruption shows the MRP-L4 product to be indispensable for mt function in cells growing on non-fermentable carbon sources. In contrast to nearly all other MRPs investigated so far, gene disruption of MRP-L4 also affects growth of yeast cells on fermentable carbon sources, suggesting additional cytosolic and/or mt functions of YmL4 besides its involvement in mt protein biosynthesis.
引用
收藏
页码:107 / 112
页数:6
相关论文
共 23 条
[1]   TRANSFORMATION OF YEAST BY A REPLICATING HYBRID PLASMID [J].
BEGGS, JD .
NATURE, 1978, 275 (5676) :104-109
[2]   EUKARYOTIC START AND STOP TRANSLATION SITES [J].
CAVENER, DR ;
RAY, SC .
NUCLEIC ACIDS RESEARCH, 1991, 19 (12) :3185-3192
[3]   FUNCTIONAL-ANALYSIS OF THE REGULATORY REGION ADJACENT TO THE CARG-B GENE OF SACCHAROMYCES-CEREVISIAE - NUCLEOTIDE-SEQUENCE, GENE FUSION EXPERIMENTS AND CIS-DOMINANT REGULATORY MUTATION ANALYSIS [J].
DEGOLS, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1987, 169 (01) :193-200
[4]  
FEARON K, 1992, J BIOL CHEM, V267, P5162
[5]  
GRAACK HR, 1988, FEBS LETT, V242, P1
[6]   THE YEAST NUCLEAR GENE MRP-L13 CODES FOR A PROTEIN OF THE LARGE SUBUNIT OF THE MITOCHONDRIAL RIBOSOME [J].
GROHMANN, L ;
KITAKAWA, M ;
ISONO, K ;
GOLDSCHMIDTREISIN, S ;
GRAACK, HR .
CURRENT GENETICS, 1994, 26 (01) :8-14
[7]   TARGETING OF ESCHERICHIA-COLI BETA-GALACTOSIDASE TO THE NUCLEUS IN YEAST [J].
HALL, MN ;
HEREFORD, L ;
HERSKOWITZ, I .
CELL, 1984, 36 (04) :1057-1065
[8]   THE NAM2 PROTEINS FROM S-CEREVISIAE AND S-DOUGLASII ARE MITOCHONDRIAL LEUCYL-TRANSFER RNA-SYNTHETASES, AND ARE INVOLVED IN MESSENGER-RNA SPLICING [J].
HERBERT, CJ ;
LABOUESSE, M ;
DUJARDIN, G ;
SLONIMSKI, PP .
EMBO JOURNAL, 1988, 7 (02) :473-483
[9]  
KAMPER U, 1992, MOL CELL BIOL, V12, P499
[10]  
KENNELLY PJ, 1991, J BIOL CHEM, V266, P15555