|Name:||ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide|
|PubMed (2687158):|| Neckelmann N, Warner CK, Chung A, Kudoh J, Minoshima S, Fukuyama R, MaekawaM, Shimizu Y, Shimizu N, Liu JD, et al. The human ATP synthase beta subunit gene: sequence analysis, chromosomeassignment, and differential expression.Genomics. 1989 Nov;5(4):829-43. PMID: 2687158 [PubMed - indexed for MEDLINE]|
In humans, the functional F0F1-ATP synthase beta subunit gene is located on chromosome 12 in the p13----qter region. Other partially homologous sequences have been detected on chromosomes 2 and 17. The bona fide beta subunit gene has 10 exons encoding a leader peptide of 49 amino acids and a mature protein of 480 amino acids. Thirteen Alu family DNA repeats are found upstream from the gene and in four introns. The gene has four "CCAAT" sequences upstream and in close proximity to the transcriptional initiation site. A 13-bp motif is found in the 5' nontranscribed region of both the beta subunit gene and an ADP/ATP translocator gene that is expressed in high levels in cardiac and skeletal muscle. Analysis of the beta subunit mRNA levels reveals marked differences among tissues. The highest levels are found in heart, lower levels in skeletal muscle, and the lowest levels in liver and kidney. These findings suggest that the tissue-specific levels of ATP synthase beta subunit mRNA may be generated through transcriptional control.