AI Article Synopsis

  • The human fast skeletal troponin T (TNNT3) gene is located on chromosome 11p15.5 and consists of 19 exons and 18 introns, with some exons being constitutively spliced and others alternatively spliced during development.
  • The gene's structure includes specific exons that are regulated during development, with evidence suggesting exon shuffling at the 5' end, while 3' exons show conservation, hinting at an evolutionary link to an ancient gene.
  • The sequence includes various transcription factor binding sites that may influence gene regulation, revealing insights into the gene's evolutionary divergence and its complex splicing mechanisms, with nucleotide sequence data stored in major genetic databases.

Article Abstract

We describe the cloning, sequencing and structure of the human fast skeletal troponin T (TNNT3) gene located on chromosome 11p15.5. The single-copy gene encodes 19 exons and 18 introns. Eleven of these exons, 1-3, 9-15 and 18, are constitutively spliced, whereas exons 4-8 are alternatively spliced. The gene contains an additional subset of developmentally regulated and alternatively spliced exons, including a foetal exon located between exon 8 and 9 and exon 16 or alpha (adult) and 17 or beta (foetal and neonatal). Exon phasing suggests that the majority of the alternatively spliced exons located at the 5' end of the gene may have evolved as a result of exon shuffling, because they are of the same phase class. In contrast, the 3' exons encoding an evolutionarily conserved heptad repeat domain, shared by both TnT and troponin I (TnI), may be remnants of an ancient ancestral gene. The sequence of the 5' flanking region shows that the putative promoter contains motifs including binding sites for MyoD, MEF-2 and several transcription factors which may play a role in transcriptional regulation and tissue-specific expression of TnT. The coding region of TNNT3 exhibits strong similarity to the corresponding rat sequence. However, unlike the rat TnT gene, TNNT3 possesses two repeat regions of CCA and TC. The exclusive presence of these repetitive elements in the human gene indicates divergence in the evolutionary dynamics of mammalian TnT genes. Homologous muscle-specific splicing enhancer motifs are present in the introns upstream and downstream of the foetal exon, and may play a role in the developmental pattern of alternative splicing of the gene. The genomic correlates of TNNT3 are relevant to our understanding of the evolution and regulation of expression of the gene, as well as the structure and function of the protein isoforms. The nucleotide sequence of TNNT3 has been submitted to EMBL/GenBank under Accession No. AF026276.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447309PMC
http://dx.doi.org/10.1002/cfg.343DOI Listing

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