Literature DB >> 18039871

Phylogenetic and genomewide analyses suggest a functional relationship between kayak, the Drosophila fos homolog, and fig, a predicted protein phosphatase 2c nested within a kayak intron.

Stephanie G Hudson1, Matthew J Garrett, Joseph W Carlson, Gos Micklem, Susan E Celniker, Elliott S Goldstein, Stuart J Newfeld.   

Abstract

A gene located within the intron of a larger gene is an uncommon arrangement in any species. Few of these nested gene arrangements have been explored from an evolutionary perspective. Here we report a phylogenetic analysis of kayak (kay) and fos intron gene (fig), a divergently transcribed gene located in a kay intron, utilizing 12 Drosophila species. The evolutionary relationship between these genes is of interest because kay is the homolog of the proto-oncogene c-fos whose function is modulated by serine/threonine phosphorylation and fig is a predicted PP2C phosphatase specific for serine/threonine residues. We found that, despite an extraordinary level of diversification in the intron-exon structure of kay (11 inversions and six independent exon losses), the nested arrangement of kay and fig is conserved in all species. A genomewide analysis of protein-coding nested gene pairs revealed that approximately 20% of nested pairs in D. melanogaster are also nested in D. pseudoobscura and D. virilis. A phylogenetic examination of fig revealed that there are three subfamilies of PP2C phosphatases in all 12 species of Drosophila. Overall, our phylogenetic and genomewide analyses suggest that the nested arrangement of kay and fig may be due to a functional relationship between them.

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Year:  2007        PMID: 18039871      PMCID: PMC2147949          DOI: 10.1534/genetics.107.071670

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  30 in total

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Authors:  M Long
Journal:  Curr Opin Genet Dev       Date:  2001-12       Impact factor: 5.578

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Authors:  S J Newfeld; R G Wisotzkey; S Kumar
Journal:  Genetics       Date:  1999-06       Impact factor: 4.562

3.  Drosophila Fos mediates ERK and JNK signals via distinct phosphorylation sites.

Authors:  L Ciapponi; D B Jackson; M Mlodzik; D Bohmann
Journal:  Genes Dev       Date:  2001-06-15       Impact factor: 11.361

4.  The gene structure of the Drosophila melanogaster homolog of the human proto-oncogene fos.

Authors:  E Rousseau; E S Goldstein
Journal:  Gene       Date:  2001-07-11       Impact factor: 3.688

5.  Response of Djun and Dfos mRNA abundance to signal transduction pathways in cultured cells of Drosophila melanogaster.

Authors:  X Xia; E S Goldstein
Journal:  Mol Biol Rep       Date:  1999-08       Impact factor: 2.316

6.  Molecular cloning and characterization of a novel human protein phosphatase 2C cDNA (PP2C epsilon*).

Authors:  Feng Jin; Chaoneng Ji; Lingfeng Liu; Jianfeng Dai; Shaohua Gu; Xianfei Sun; Yi Xie; Yumin Mao
Journal:  Mol Biol Rep       Date:  2004-09       Impact factor: 2.316

7.  The gene structure of the Drosophila melanogaster proto-oncogene, kayak, and its nested gene, fos-intronic gene.

Authors:  Stephanie Gidget Hudson; Elliott S Goldstein
Journal:  Gene       Date:  2008-05-10       Impact factor: 3.688

8.  Rates and patterns of chromosomal evolution in Drosophila pseudoobscura and D. miranda.

Authors:  Carolina Bartolomé; Brian Charlesworth
Journal:  Genetics       Date:  2006-03-17       Impact factor: 4.562

9.  Drosophila puckered regulates Fos/Jun levels during follicle cell morphogenesis.

Authors:  L L Dobens; E Martín-Blanco; A Martínez-Arias; F C Kafatos; L A Raftery
Journal:  Development       Date:  2001-05       Impact factor: 6.868

10.  The genome sequence of Drosophila melanogaster.

Authors:  M D Adams; S E Celniker; R A Holt; C A Evans; J D Gocayne; P G Amanatides; S E Scherer; P W Li; R A Hoskins; R F Galle; R A George; S E Lewis; S Richards; M Ashburner; S N Henderson; G G Sutton; J R Wortman; M D Yandell; Q Zhang; L X Chen; R C Brandon; Y H Rogers; R G Blazej; M Champe; B D Pfeiffer; K H Wan; C Doyle; E G Baxter; G Helt; C R Nelson; G L Gabor; J F Abril; A Agbayani; H J An; C Andrews-Pfannkoch; D Baldwin; R M Ballew; A Basu; J Baxendale; L Bayraktaroglu; E M Beasley; K Y Beeson; P V Benos; B P Berman; D Bhandari; S Bolshakov; D Borkova; M R Botchan; J Bouck; P Brokstein; P Brottier; K C Burtis; D A Busam; H Butler; E Cadieu; A Center; I Chandra; J M Cherry; S Cawley; C Dahlke; L B Davenport; P Davies; B de Pablos; A Delcher; Z Deng; A D Mays; I Dew; S M Dietz; K Dodson; L E Doup; M Downes; S Dugan-Rocha; B C Dunkov; P Dunn; K J Durbin; C C Evangelista; C Ferraz; S Ferriera; W Fleischmann; C Fosler; A E Gabrielian; N S Garg; W M Gelbart; K Glasser; A Glodek; F Gong; J H Gorrell; Z Gu; P Guan; M Harris; N L Harris; D Harvey; T J Heiman; J R Hernandez; J Houck; D Hostin; K A Houston; T J Howland; M H Wei; C Ibegwam; M Jalali; F Kalush; G H Karpen; Z Ke; J A Kennison; K A Ketchum; B E Kimmel; C D Kodira; C Kraft; S Kravitz; D Kulp; Z Lai; P Lasko; Y Lei; A A Levitsky; J Li; Z Li; Y Liang; X Lin; X Liu; B Mattei; T C McIntosh; M P McLeod; D McPherson; G Merkulov; N V Milshina; C Mobarry; J Morris; A Moshrefi; S M Mount; M Moy; B Murphy; L Murphy; D M Muzny; D L Nelson; D R Nelson; K A Nelson; K Nixon; D R Nusskern; J M Pacleb; M Palazzolo; G S Pittman; S Pan; J Pollard; V Puri; M G Reese; K Reinert; K Remington; R D Saunders; F Scheeler; H Shen; B C Shue; I Sidén-Kiamos; M Simpson; M P Skupski; T Smith; E Spier; A C Spradling; M Stapleton; R Strong; E Sun; R Svirskas; C Tector; R Turner; E Venter; A H Wang; X Wang; Z Y Wang; D A Wassarman; G M Weinstock; J Weissenbach; S M Williams; K C Worley; D Wu; S Yang; Q A Yao; J Ye; R F Yeh; J S Zaveri; M Zhan; G Zhang; Q Zhao; L Zheng; X H Zheng; F N Zhong; W Zhong; X Zhou; S Zhu; X Zhu; H O Smith; R A Gibbs; E W Myers; G M Rubin; J C Venter
Journal:  Science       Date:  2000-03-24       Impact factor: 47.728

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  4 in total

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Journal:  Dev Biol       Date:  2015-07-21       Impact factor: 3.582

3.  Family size and turnover rates among several classes of small non-protein-coding RNA genes in Caenorhabditis nematodes.

Authors:  Paul Po-Shen Wang; Ilya Ruvinsky
Journal:  Genome Biol Evol       Date:  2012-03-30       Impact factor: 3.416

4.  2mit, an intronic gene of Drosophila melanogaster timeless2, is involved in behavioral plasticity.

Authors:  Francesca Baggio; Andrea Bozzato; Clara Benna; Emanuela Leonardi; Ottavia Romoli; Moira Cognolato; Silvio C E Tosatto; Rodolfo Costa; Federica Sandrelli
Journal:  PLoS One       Date:  2013-09-30       Impact factor: 3.240

  4 in total

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