Literature DB >> 8028024

Nucleotide sequence of the genomic region encompassing Adh and Adh-dup genes of D. lebanonensis (Scaptodrosophila): gene expression and evolutionary relationships.

E Juan1, M Papaceit, A Quintana.   

Abstract

The region of the genome of D. lebanonensis that contains the Adh gene and the downstream Adh-dup gene was sequenced. The structure of the two genes is the same as has been described for D. melanogaster. Adh has two promoters and Adh-dup has only one putative promoter. The levels of expression of the two genes in this species are dramatically different. Hybridizing the same Northern blots with a specific probe for Adh-dup, we did not find transcripts for this gene in D. lebanonensis. The level of Adh distal transcript in adults of D. lebanonensis is five times greater than that of D. melanogaster adults. The maximum levels of proximal transcript are attained at different larval stages in the two species, being three times higher in D. melanogaster late-second-instar larvae than in D. lebanonensis first-instar larvae. The level of Adh transcripts allowed us to determine distal and proximal initiation transcription sites, the position of the first intron, the use of two polyadenylation signals, and the heterogeneity of polyadenylation sites. Temporal and spatial expression profiles of the Adh gene of D. lebanonensis show qualitative differences compared with D. melanogaster. Adh and Adh-dup evolve differently as shown by the synonymous and nonsynonymous substitution rates for the coding region of both genes when compared across two species of the melanogaster group, two of the obscura group of the subgenus Sophophora and D. lebanonensis of the victoria group of the subgenus Scaptodrsophila. Synonymous rates for Adh are approximately half those for Adh-dup, while nonsynonymous rates for Adh are generally higher than those for Adh-dup. Adh shows 76.8% identities at the protein level and 70.2% identities at the nucleotide level while Adh-dup shows 83.7% identities at the protein level and 67.5% identities at the nucleotide level. Codon usage for Adh-dup is shown to be less biased than for Adh, which could explain the higher synonymous rates and the generally lower nonsynonymous substitution rates in Adh-dup compared with Adh. Phylogenetic trees reconstructed by distance matrix and parsimony methods show that Sophophora and Scaptodrosophila subgenera diverged shortly after the separation from the Drosophila subgenus.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8028024     DOI: 10.1007/bf00178845

Source DB:  PubMed          Journal:  J Mol Evol        ISSN: 0022-2844            Impact factor:   2.395


  38 in total

1.  Nucleotide sequence of the Adh gene of Drosophila lebanonensis.

Authors:  E Juan; M Papaceit; A Quintana
Journal:  Nucleic Acids Res       Date:  1990-11-11       Impact factor: 16.971

2.  Inferring the evolutionary histories of the Adh and Adh-dup loci in Drosophila melanogaster from patterns of polymorphism and divergence.

Authors:  M Kreitman; R R Hudson
Journal:  Genetics       Date:  1991-03       Impact factor: 4.562

3.  Translation is required for regulation of histone mRNA degradation.

Authors:  R A Graves; N B Pandey; N Chodchoy; W F Marzluff
Journal:  Cell       Date:  1987-02-27       Impact factor: 41.582

4.  A shift in the third-codon-position nucleotide frequency in alcohol dehydrogenase genes in the genus Drosophila.

Authors:  W T Starmer; D T Sullivan
Journal:  Mol Biol Evol       Date:  1989-09       Impact factor: 16.240

5.  The neighbor-joining method: a new method for reconstructing phylogenetic trees.

Authors:  N Saitou; M Nei
Journal:  Mol Biol Evol       Date:  1987-07       Impact factor: 16.240

Review 6.  A new method for estimating synonymous and nonsynonymous rates of nucleotide substitution considering the relative likelihood of nucleotide and codon changes.

Authors:  W H Li; C I Wu; C C Luo
Journal:  Mol Biol Evol       Date:  1985-03       Impact factor: 16.240

7.  The messenger RNA for alcohol dehydrogenase in Drosophila melanogaster differs in its 5' end in different developmental stages.

Authors:  C Benyajati; N Spoerel; H Haymerle; M Ashburner
Journal:  Cell       Date:  1983-05       Impact factor: 41.582

8.  Tissue-specific regulatory differences for the alcohol dehydrogenase genes of Hawaiian Drosophila are conserved in Drosophila melanogaster transformants.

Authors:  M D Brennan; C Y Wu; A J Berry
Journal:  Proc Natl Acad Sci U S A       Date:  1988-09       Impact factor: 11.205

9.  The Adh genomic region of Drosophila ambigua: evolutionary trends in different species.

Authors:  G Marfany; R Gonzàlez-Duarte
Journal:  J Mol Evol       Date:  1991-06       Impact factor: 2.395

10.  Nucleotide sequence of the genomic region encoding alcohol dehydrogenase in Drosophila affinidisjuncta.

Authors:  R G Rowan; W J Dickinson
Journal:  J Mol Evol       Date:  1988 Dec-1989 Feb       Impact factor: 2.395

View more
  4 in total

1.  Molecular organization of the Drosophila melanogaster Adh chromosomal region in D. repleta and D. buzzatii, two distantly related species of the Drosophila subgenus.

Authors:  J González; E Betrán; M Ashburner; A Ruiz
Journal:  Chromosome Res       Date:  2000       Impact factor: 5.239

2.  Synonymous substitutions in the Xdh gene of Drosophila: heterogeneous distribution along the coding region.

Authors:  J M Comeron; M Aguadé
Journal:  Genetics       Date:  1996-11       Impact factor: 4.562

3.  Exploring the evolutionary history of the alcohol dehydrogenase gene (Adh) duplication in species of the family tephritidae.

Authors:  George N Goulielmos; Michael Loukas; George Bondinas; Eleftherios Zouros
Journal:  J Mol Evol       Date:  2003-08       Impact factor: 2.395

4.  Sequences upstream of the homologous cis-elements of the Adh adult enhancer of Drosophila are required for maximal levels of Adh gene transcription in adults of Scaptodrosophila lebanonensis.

Authors:  Montserrat Papaceit; Dorcas Orengo; Elvira Juan
Journal:  Genetics       Date:  2004-05       Impact factor: 4.562

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.