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Published on: March 3, 2015
Promoter analysis of the PDA1 gene encoding the E1 alpha subunit of the pyruvate dehydrogenase complex from
T J Wenzel1, A M Zuurmond, A Bergmans
1Department of Molecular and Cellular Biology, Leiden University, The Netherlands.
Insights
Researchers identified the location and sequence of the PDA1 gene in yeast, crucial for pyruvate dehydrogenase (PDH) complex function. Deletion analysis revealed a key 42 bp region essential for PDA1 gene transcription.
Area of Science:
- Molecular Biology
- Yeast Genetics
- Gene Regulation
Background:
- The pyruvate dehydrogenase (PDH) complex is vital for cellular energy metabolism.
- Understanding the regulation of genes encoding PDH subunits, like PDA1, is crucial for metabolic studies.
Purpose of the Study:
- To determine the precise location and sequence of the PDA1 gene in Saccharomyces cerevisiae.
- To identify and characterize regulatory elements within the PDA1 promoter that control its transcription.
Main Methods:
- Gene mapping using genetic linkage analysis.
- DNA sequencing of the PDA1 gene and its promoter region.
- Deletion analysis of the PDA1 promoter using ExoIII nuclease.
- Transcriptional analysis via Northern blotting.
Main Results:
- The PDA1 gene was localized to chromosome V, 4 cM from the RAD3 gene.
- Sequencing revealed the PDA1 open reading frame and its promoter, including a putative GCN4 binding site.
- A critical 42 bp region (-190 to -148 bp relative to ATG) was identified as essential for PDA1 promoter activity, reducing transcription >40-fold upon deletion.
- No canonical TATA box or known yeast regulatory motifs were found in the essential region.
Conclusions:
- The PDA1 gene's location and sequence were established in yeast.
- A novel, essential regulatory element within the PDA1 promoter, independent of TATA boxes, was identified.
- The CCCTT sequence in this region may play a role in regulating PDH subunit gene expression.
Abstract:
The location and sequence of the PDA1 gene, encoding the E1 alpha subunit of the pyruvate dehydrogenase (PDH) complex from Saccharomyces cerevisiae, were determined. The PDA1 gene was located on a 6.2 kb fragment of chromosome V, approximately 18 kb centromere distal to RAD3. Consistent with this, the PDA1 gene was genetically mapped at 4 cM from RAD3. A part of the 6.2 kb fragment of chromosome V was sequenced. The nucleotide sequence contained the PDA1 open reading frame and the entire putative promoter. Computer analysis revealed a putative GCN4 binding motif in the PDA1 promoter. The presence of transcriptional elements was experimentally determined by deletion analysis. To this end, ExoIII deletions were constructed in the 5' to 3' direction of the PDA1 promoter and effects on transcription were determined by Northern analysis. Transcription was unaffected upon deletion to position -190 relative to the ATG start codon. Deletions from position -148 and beyond, however, reduced promoter activity at least 40-fold. Apparently the 42 bp between nucleotides -190 and -148 contain an element essential for transcription. Inactivation of the PDA1 promoter could not be attributed to deletions of a recognizable TATA element or any known yeast regulatory motifs. The possible role of the CCCTT sequence present in the 42 bp region and also in the promoters of the other genes encoding subunits of the PDH complex is discussed.
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