Alternative Splicing Regulates Targeting of Malate Dehydrogenase in Yarrowia lipolytica

被引:43
作者
Kabran, Philomene [1 ,2 ]
Rossignol, Tristan [1 ]
Gaillardin, Claude [3 ]
Nicaud, Jean-Marc [4 ]
Neuveglise, Cecile [1 ]
机构
[1] INRA, UMR Micalis 1319, F-78352 Jouy En Josas, France
[2] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[3] AgroParisTech, F-78352 Jouy En Josas, France
[4] CNRS, F-78352 Jouy En Josas, France
关键词
yeast; TCA cycle; glyoxylate cycle; MDH2; intron; MULTIPLE SEQUENCE ALIGNMENT; UNFOLDED PROTEIN RESPONSE; SACCHAROMYCES-CEREVISIAE; GLYOXYLATE CYCLE; MESSENGER-RNAS; PEROXISOMAL MEMBRANE; ACETATE METABOLISM; GENE-EXPRESSION; BETA-OXIDATION; YEAST;
D O I
10.1093/dnares/dss007
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Alternative pre-mRNA splicing is a major mechanism contributing to the proteome complexity of most eukaryotes, especially mammals. In less complex organisms, such as yeasts, the numbers of genes that contain introns are low and cases of alternative splicing (AS) with functional implications are rare. We report the first case of AS with functional consequences in the yeast Yarrowia lipolytica. The splicing pattern was found to govern the cellular localization of malate dehydrogenase, an enzyme of the central carbon metabolism. This ubiquitous enzyme is involved in the tricarboxylic acid cycle in mitochondria and in the glyoxylate cycle, which takes place in peroxisomes and the cytosol. In Saccharomyces cerevisiae, three genes encode three compartment-specific enzymes. In contrast, only two genes exist in Y. lipolytica. One gene (YIMDH1, YALI0D16753g) encodes a predicted mitochondrial protein, whereas the second gene (YIMDH2, YALI0E14190g) generates the cytosolic and peroxisomal forms through the alternative use of two 3'-splice sites in the second intron. Both splicing variants were detected in cDNA libraries obtained from cells grown under different conditions. Mutants expressing the individual YlMdh2p isoforms tagged with fluorescent proteins confirmed that they localized to either the cytosolic or the peroxisomal compartment.
引用
收藏
页码:231 / 244
页数:14
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