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Molecular evolution at the decapentaplegic locus in Drosophila.
- Source :
-
Genetics [Genetics] 1997 Feb; Vol. 145 (2), pp. 297-309. - Publication Year :
- 1997
-
Abstract
- Using an elaborate set of cis-regulatory sequences, the decapentaplegic (dpp) gene displays a dynamic pattern of gene expression during development. The C-terminal portion of the DPP protein is processed to generate a secreted signaling molecule belonging to the transforming growth factor-beta (TGF-beta) family. This signal, the DPP ligand, is able to influence the developmental fates of responsive cells in a concentration-dependent fashion. Here we examine the sequence level organization of a significant portion of the dpp locus in Drosophila melanogaster and use interspecific comparisons with D. simulans, D. pseudoobscura and D.virilis to explore the molecular evolution of the gene. Our interspecific analysis identified significant selective constraint on both the nucleotide and amino acid sequences. As expected, interspecific comparison of protein coding sequences shows that the C-terminal ligand region is highly conserved. However, the central portion of the protein is also conserved, while the N-terminal third is quite variable. Comparison of noncoding regions reveals significant stretches of nucleotide identity in the 3' untranslated portion of exon 3 and in the intron between exons 2 and 3. An examination of cDNA sequences representing five classes of dpp transcripts indicates that these transcripts encode the same polypeptide.
- Subjects :
- Amino Acid Sequence
Animals
Base Sequence
Chromosome Mapping
DNA
Evolution, Molecular
Introns
Molecular Sequence Data
Protein Biosynthesis
Sequence Homology, Amino Acid
Drosophila genetics
Drosophila Proteins
Drosophila melanogaster genetics
Insect Proteins genetics
Transforming Growth Factor beta genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0016-6731
- Volume :
- 145
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 9071585
- Full Text :
- https://doi.org/10.1093/genetics/145.2.297