- THIS ARTICLE
- Full Text (PDF)
- Alert me when this article is cited
- Alert me if a correction is posted
- SERVICES
- Similar articles in this journal
- Similar articles in PubMed
- Alert me to new issues of the journal
- Download to citation manager
- Reprints & Permissions
- CITING ARTICLES
- Citing Articles via HighWire
- Citing Articles via Google Scholar
- GOOGLE SCHOLAR
- Articles by Walsh, J. B.
- Search for Related Content
- PUBMED
- PubMed Citation
- Articles by Walsh, J. B.
HOW MANY PROCESSED PSEUDOGENES ARE ACCUMULATED IN A GENE FAMILY?
James Bruce Walsh 1
1 Department of Molecular Genetics and Cell Biology, The University
of Chicago, Chicago, Illinois 60637
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
per gene and is countered by spontaneous deletion (at
rate
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(
/
), and the percentage
of functional genes in the gene family at equilibrium is 1/[1 + (
/
)].
/
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
is
sufficiently large relative to the per nucleotide mutation rate µ (
>
20µ), 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.
Anything produced by evolution is bound to be a bit of a messS. Brenner
Submitted on October 30, 1984Accepted on February 19, 1985
This article has been cited by other articles:
![]() |
A. Baumgarten, S. Cannon, R. Spangler, and G. May Genome-Level Evolution of Resistance Genes in Arabidopsis thaliana Genetics, September 1, 2003; 165(1): 309 - 319. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Dvornyk, O. Vinogradova, and E. Nevo Origin and evolution of circadian clock genes in prokaryotes PNAS, March 4, 2003; 100(5): 2495 - 2500. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Dvornyk, O. Vinogradova, and E. Nevo 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 PNAS, February 6, 2002; (2002) 261699498. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Lynch, M. O'Hely, B. Walsh, and A. Force The Probability of Preservation of a Newly Arisen Gene Duplicate Genetics, December 1, 2001; 159(4): 1789 - 1804. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Lynch and J. S. Conery The Evolutionary Fate and Consequences of Duplicate Genes Science, November 10, 2000; 290(5494): 1151 - 1155. [Abstract] [Full Text] |
||||
![]() |
M. Lynch and A. Force The Probability of Duplicate Gene Preservation by Subfunctionalization Genetics, January 1, 2000; 154(1): 459 - 473. [Abstract] [Full Text] |
||||
![]() |
R. Lum and M. L. Linial Retrotransposition of Nonviral RNAs in an Avian Packaging Cell Line J. Virol., May 1, 1998; 72(5): 4057 - 4064. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Dvornyk, O. Vinogradova, and E. Nevo 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 PNAS, February 19, 2002; 99(4): 2082 - 2087. [Abstract] [Full Text] [PDF] |
||||



