A widespread transposable element masks expression of a yeast copper transport gene

被引:219
作者
Knight, SAB
Labbe, S
Kwon, LF
Kosman, DJ
Thiele, DJ
机构
[1] UNIV MICHIGAN, SCH MED, DEPT BIOL CHEM, ANN ARBOR, MI 48109 USA
[2] SUNY BUFFALO, SCH MED & BIOMED SCI, DEPT BIOCHEM, BUFFALO, NY 14214 USA
关键词
copper; transport; yeast; transposon; transcription;
D O I
10.1101/gad.10.15.1917
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The trace element copper (Cu) is essential for cell growth. In this report we describe the identification of a new component of the high-affinity Cu transport machinery in yeast, encoded by the CTR3 gene. Ctr3p is a small intracellular cysteine-rich integral membrane protein that restores high-affinity Cu uptake, Cu, Zn superoxide dismutase activity, ferrous iron transport, and respiratory proficiency to strains lacking the CTR1 (Cu transporter 1) gene. In most commonly used Saccharomyces cerevisiae laboratory strains, expression of CTR3 is abolished by a Ty2 transposon insertion that separates the CTR3 promoter from the transcriptional start sites by 6 kb. In strains that do not possess a Ty2 transposon at the CTR3 locus, expression of CTR3 is repressed by copper and activated by copper starvation. In such strains inactivation of both CTR1 and CTR3 is required to generate lethal copper-deficient phenotypes. Although Ctr1p and Ctr3p can function independently in copper transport, the expression of both proteins provides maximal copper uptake and growth rate under copper-limiting conditions. These results underscore the importance of mobile DNA elements in the alteration of gene function and phenotypic variation.
引用
收藏
页码:1917 / 1929
页数:13
相关论文
共 60 条
[21]   OXYGEN-TOXICITY, OXYGEN RADICALS, TRANSITION-METALS AND DISEASE [J].
HALLIWELL, B ;
GUTTERIDGE, JMC .
BIOCHEMICAL JOURNAL, 1984, 219 (01) :1-14
[22]   EVIDENCE FOR CU(II) REDUCTION AS A COMPONENT OF COPPER UPTAKE BY SACCHAROMYCES-CEREVISIAE [J].
HASSETT, R ;
KOSMAN, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (01) :128-134
[23]   ENDOSOMES [J].
HELENIUS, A ;
MELLMAN, I ;
WALL, D ;
HUBBARD, A .
TRENDS IN BIOCHEMICAL SCIENCES, 1983, 8 (07) :245-250
[24]   TRANSFORMATION OF INTACT YEAST-CELLS TREATED WITH ALKALI CATIONS [J].
ITO, H ;
FUKUDA, Y ;
MURATA, K ;
KIMURA, A .
JOURNAL OF BACTERIOLOGY, 1983, 153 (01) :163-168
[25]   IDENTIFICATION OF A CONSENSUS MOTIF FOR RETENTION OF TRANSMEMBRANE PROTEINS IN THE ENDOPLASMIC-RETICULUM [J].
JACKSON, MR ;
NILSSON, T ;
PETERSON, PA .
EMBO JOURNAL, 1990, 9 (10) :3153-3162
[26]  
KAMPFENKEL K, 1995, J BIOL CHEM, V270, P28479, DOI 10.1074/jbc.270.47.28479
[27]  
Kleckner N., 1989, Mobile DNA, P227
[28]   THE ABC-TRANSPORTER STE6 ACCUMULATES IN THE PLASMA-MEMBRANE IN A UBIQUITINATED FORM IN ENDOCYTOSIS MUTANTS [J].
KOLLING, R ;
HOLLENBERG, CP .
EMBO JOURNAL, 1994, 13 (14) :3261-3271
[29]  
KOLODZIEJ PA, 1991, METHOD ENZYMOL, V194, P508
[30]   THE A-FACTOR TRANSPORTER (STE6 GENE-PRODUCT) AND CELL POLARITY IN THE YEAST SACCHAROMYCES-CEREVISIAE [J].
KUCHLER, K ;
DOHLMAN, HG ;
THORNER, J .
JOURNAL OF CELL BIOLOGY, 1993, 120 (05) :1203-1215