Literature DB >> 2408963

How many processed pseudogenes are accumulated in a gene family?

J B Walsh.   

Abstract

A simple kinetic model is developed that describes the accumulation of processed pseudogenes in a functional gene family. Insertion of new pseudogenes occurs at rate v per gene and is countered by spontaneous deletion (at rate delta per DNA segment) of segments containing processed pseudogenes. If there are k functional genes in a gene family, the equilibrium number of processed pseudogenes is k(v/delta), and the percentage of functional genes in the gene family at equilibrium is 1/[1 + (v/delta)]. v/delta values estimated for five gene families ranged from 1.7 to 15. This fairly narrow range suggests that the rates of formation and deletion of processed pseudogenes may be positively correlated for these families. If delta is sufficiently large relative to the per nucleotide mutation rate mu (delta greater than 20 mu), processed pseudogenes will show high homology with each other, even in the absence of gene conversion between pseudogenes. We argue that formation of processed pseudogenes may share common pathways with transposable elements and retroviruses, creating the potential for correlated responses in the evolution of processed pseudogenes due to direct selection for control of transposable elements and/or retroviruses. Finally, we discuss the nature of the selective forces that may act directly or indirectly to influence the evolution of processed pseudogenes.

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Year:  1985        PMID: 2408963      PMCID: PMC1202568     

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


  45 in total

Review 1.  The tubulins: from DNA to RNA to protein and back again.

Authors:  D W Cleveland
Journal:  Cell       Date:  1983-09       Impact factor: 41.582

2.  A straight LINE story.

Authors:  J Rogers
Journal:  Nature       Date:  1983 Nov 10-16       Impact factor: 49.962

3.  Non-Alu family interspersed repeats in human DNA and their transcriptional activity.

Authors:  L Sun; K E Paulson; C W Schmid; L Kadyk; L Leinwand
Journal:  Nucleic Acids Res       Date:  1984-03-26       Impact factor: 16.971

4.  Selfish DNAs with self-restraint.

Authors:  W F Doolittle; T B Kirkwood; M A Dempster
Journal:  Nature       Date:  1984 Feb 9-15       Impact factor: 49.962

5.  The human c-Ha-ras2 is a processed pseudogene inactivated by numerous base substitutions.

Authors:  J Miyoshi; M Kagimoto; E Soeda; Y Sakaki
Journal:  Nucleic Acids Res       Date:  1984-02-24       Impact factor: 16.971

6.  Transposable element IS50 improves growth rate of E. coli cells without transposition.

Authors:  D L Hartl; D E Dykhuizen; R D Miller; L Green; J de Framond
Journal:  Cell       Date:  1983-12       Impact factor: 41.582

7.  A processed human immunoglobulin epsilon gene has moved to chromosome 9.

Authors:  J Battey; E E Max; W O McBride; D Swan; P Leder
Journal:  Proc Natl Acad Sci U S A       Date:  1982-10       Impact factor: 11.205

8.  Tissue-specific expression of a chicken calmodulin pseudogene lacking intervening sequences.

Authors:  J P Stein; R P Munjaal; L Lagace; E C Lai; B W O'Malley; A R Means
Journal:  Proc Natl Acad Sci U S A       Date:  1983-11       Impact factor: 11.205

9.  A large interspersed repeat found in mouse DNA contains a long open reading frame that evolves as if it encodes a protein.

Authors:  S L Martin; C F Voliva; F H Burton; M H Edgell; C A Hutchison
Journal:  Proc Natl Acad Sci U S A       Date:  1984-04       Impact factor: 11.205

10.  Evaluating the conditions of patients with congestive heart failure by exercise testing.

Authors:  D A Weiner
Journal:  Arch Intern Med       Date:  1983-10
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  9 in total

1.  Long-term microclimatic stress causes rapid adaptive radiation of kaiABC clock gene family in a cyanobacterium, Nostoc linckia, from "Evolution Canyons" I and II, Israel.

Authors:  Volodymyr Dvornyk; Oxana Vinogradova; Eviatar Nevo
Journal:  Proc Natl Acad Sci U S A       Date:  2002-02-12       Impact factor: 11.205

2.  Origin and evolution of circadian clock genes in prokaryotes.

Authors:  Volodymyr Dvornyk; Oxana Vinogradova; Eviatar Nevo
Journal:  Proc Natl Acad Sci U S A       Date:  2003-02-25       Impact factor: 11.205

3.  Genome-level evolution of resistance genes in Arabidopsis thaliana.

Authors:  Andrew Baumgarten; Steven Cannon; Russ Spangler; Georgiana May
Journal:  Genetics       Date:  2003-09       Impact factor: 4.562

4.  Specificity of retroviral RNA packaging.

Authors:  R Aronoff; M Linial
Journal:  J Virol       Date:  1991-01       Impact factor: 5.103

5.  Retrotransposition of nonviral RNAs in an avian packaging cell line.

Authors:  R Lum; M L Linial
Journal:  J Virol       Date:  1998-05       Impact factor: 5.103

6.  Population genetics of an expanding family of mobile genetic elements.

Authors:  T Ohta
Journal:  Genetics       Date:  1986-05       Impact factor: 4.562

7.  Variable Rates of Simple Satellite Gains across the Drosophila Phylogeny.

Authors:  Kevin H-C Wei; Sarah E Lower; Ian V Caldas; Trevor J S Sless; Daniel A Barbash; Andrew G Clark
Journal:  Mol Biol Evol       Date:  2018-04-01       Impact factor: 16.240

8.  Evolution of cytochrome c genes and pseudogenes.

Authors:  C I Wu; W H Li; J J Shen; R C Scarpulla; K J Limbach; R Wu
Journal:  J Mol Evol       Date:  1986       Impact factor: 2.395

9.  Sequence-dependent gene conversion: can duplicated genes diverge fast enough to escape conversion?

Authors:  J B Walsh
Journal:  Genetics       Date:  1987-11       Impact factor: 4.562

  9 in total

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