MYRISTIC ACID AUXOTROPHY CAUSED BY MUTATION OF SACCHAROMYCES-CEREVISIAE MYRISTOYL-COA-PROTEIN N-MYRISTOYLTRANSFERASE

被引:69
作者
DURONIO, RJ [1 ]
RUDNICK, DA [1 ]
JOHNSON, RL [1 ]
JOHNSON, DR [1 ]
GORDON, JI [1 ]
机构
[1] WASHINGTON UNIV,SCH MED,DEPT MED,ST LOUIS,MO 63110
关键词
D O I
10.1083/jcb.113.6.1313
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The S. cerevisiae myristoyl-CoA:protein N-myristoyltransferase gene (NMT1) is essential for vegetative growth. NMT1 was found to be allelic with a previously described, but unmapped and unidentified mutation that causes myristic acid (C14:0) auxotrophy. The mutant (nmt1-181) is temperature sensitive, but growth at the restrictive temperature (36-degrees-C) is rescued with exogenous C14:0. Several analogues of myristate with single oxygen or sulfur for methylene group substitutions partially complement the phenotype, while others inhibit growth even at the permissive temperature (24-degrees-C). Cerulenin, a fatty acid synthetase inhibitor, also prevents growth of the mutant at 24-degrees-C. Complementation of growth at 36-degrees-C by exogenous fatty acids is blocked by a mutation affecting the acyl:CoA synthetase gene. The nmt1-181 allele contains a single missense mutation of the 455 residue acyltransferase that results in a Gly451 --> Asp substitution. Analyses of several intragenic suppressors suggest that Gly451 is critically involved in NMT catalysis. In vitro kinetic studies with purified mutant enzyme revealed a 10-fold increase in the apparent K(m) for myristoyl-CoA at 36-degrees-C, relative to wild-type, that contributes to an observed 200-fold reduction in catalytic efficiency. Together, the data indicate that nmt-181 represents a sensitive reporter of the myristoyl-CoA pools utilized by NMT.
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页码:1313 / 1330
页数:18
相关论文
共 84 条
[1]   VECTORS BEARING A HYBRID TRP-LAC PROMOTER USEFUL FOR REGULATED EXPRESSION OF CLONED GENES IN ESCHERICHIA-COLI [J].
AMANN, E ;
BROSIUS, J ;
PTASHNE, M .
GENE, 1983, 25 (2-3) :167-178
[2]   SUBSTITUTION OF CELLULAR FATTY-ACIDS IN YEAST-CELLS BY ANTIBIOTIC CERULENIN AND EXOGENOUS FATTY-ACIDS [J].
AWAYA, J ;
OHNO, T ;
OHNO, H ;
OMURA, S .
BIOCHIMICA ET BIOPHYSICA ACTA, 1975, 409 (03) :267-273
[3]  
BLACK PN, 1987, J BIOL CHEM, V262, P1412
[4]   MYRISTOYLATION-DEPENDENT REPLICATION AND ASSEMBLY OF HUMAN IMMUNODEFICIENCY VIRUS-1 [J].
BRYANT, M ;
RATNER, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (02) :523-527
[5]   INCORPORATION OF 12-METHOXYDODECANOATE INTO THE HUMAN IMMUNODEFICIENCY VIRUS-1 GAG POLYPROTEIN PRECURSOR INHIBITS ITS PROTEOLYTIC PROCESSING AND VIRUS PRODUCTION IN A CHRONICALLY INFECTED HUMAN LYMPHOID-CELL LINE [J].
BRYANT, ML ;
RATNER, L ;
DURONIO, RJ ;
KISHORE, NS ;
DEVADAS, B ;
ADAMS, SP ;
GORDON, JI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (06) :2055-2059
[6]  
BURNETTE WN, 1981, ANAL BIOCHEM, V112, P195, DOI 10.1016/0003-2697(81)90281-5
[7]   THE ABSENCE OF MYRISTIC ACID DECREASES MEMBRANE-BINDING OF P60SRC BUT DOES NOT AFFECT TYROSINE PROTEIN-KINASE ACTIVITY [J].
BUSS, JE ;
KAMPS, MP ;
GOULD, K ;
SEFTON, BM .
JOURNAL OF VIROLOGY, 1986, 58 (02) :468-474
[8]   2 DIFFERENTIALLY REGULATED MESSENGER-RNAS WITH DIFFERENT 5' ENDS ENCODE SECRETED AND INTRACELLULAR FORMS OF YEAST INVERTASE [J].
CARLSON, M ;
BOTSTEIN, D .
CELL, 1982, 28 (01) :145-154
[9]   CONSTRUCTION AND CHARACTERIZATION OF AMPLIFIABLE MULTICOPY DNA CLONING VEHICLES DERIVED FROM P15A CRYPTIC MINIPLASMID [J].
CHANG, ACY ;
COHEN, SN .
JOURNAL OF BACTERIOLOGY, 1978, 134 (03) :1141-1156
[10]  
CHIRALA SS, 1987, J BIOL CHEM, V262, P4231