Review:Pdha-2, past and present

✍ Scribed by Young, Julia C.; Gould, Jodee A.; Kola, Ismail; Iannello, Rocco C.

• Publisher: John Wiley and Sons
• Year: 1998
• Tongue: English
• Weight: 420 KB
• Volume: 282
• Category: Article
• ISSN: 0022-104X
• DOI: 10.1002/(sici)1097-010x(199809/10)282:1/2<231::aid-jez24>3.0.co;2-v

✦ Synopsis

Pyruvate dehydrogenase (PDH) is a multiunit enzymatic complex essential for the process of generating cellular energy. One of the most important of its subunits is the E1α subunit. Perturbations in the expression of this subunit lead to reduced or lost function of the PDH complex as a whole, resulting in a loss of ATP production. The consequence of such perturbations can lead to neurological abnormalities, lactic acidosis, and in males, death. Pdha-2 codes for the mouse testis isoform of the E1α subunit and maps to chromosome 19 (chromosome 4 in humans). This is a fortuitous evolutionary development because the somatic isoform of the E1α subunit is linked to the X-chromosome, which is not only inactivated early in spermatogenesis but is represented in only half of the haploid spermatid population. Consequently, activation of the testis-specific E1α subunit is essential for the progression of spermatogenesis. Despite its importance, the molecular mechanisms governing the tight tissue-and temporal-specific regulation of Pdha-2 have, until recently, remained poorly understood. In this review, we describe our current understanding of the transcriptional regulation of Pdha-2 and propose potential mechanisms that may play a role in this process.