The Journal of Biochemistry
Online ISSN : 1756-2651
Print ISSN : 0021-924X
Expression of Tom34 Splicing Isoforms in Mouse Testis and Knock-out of Tom34 in Mice
Kazutoyo TeradaShota UenoKentaro YomogidaTomoaki ImaiHiroshi KiyonariNaoki TakedaMasato YanoShinichi AbeShinichi AizawaMasataka Mori
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2003 Volume 133 Issue 5 Pages 625-631

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Abstract
The 34-kDa translocase of the outer mitochondrial membrane (Tom34) is a putative mammalian-specific factor involved in protein import into mitochondria. We ana-lyzed the genomic sequence of the mouse Tom34 gene and found it has two alternative initial exons. Using reverse transcription and the polymerase chain reaction (RT-PCR), we found that these two mRNAs differs only in the 5'-proximal sequences corre-sponding to the two initial exons (exon 1a and 1b). Tom34 mRNA with exon 1a (Tom34a) is expressed ubiquitously, while that with exon 1b (Tom34b) is expressed only in mature testicular germ cells. To explore the in vivo function of Tom34 pro-teins, we generated Tom34-deficient mice by targeted disruption. The Tom34-|- mice were viable and grew normally and had a normal Mendelian inheritance pattern. Male as well as female Tom34-|- mice were fertile. In vitro-preprotein import into iso-lated mitochondria showed no apparent difference between Tom34-|- and wild-type mice. These results indicate that Tom34 is dispensable for mouse growth and develop-ment under optimal conditions.
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