» Articles » PMID: 10331254

Evidence for Genetic Drift in Endosymbionts (Buchnera): Analyses of Protein-coding Genes

Overview
Journal Mol Biol Evol
Specialty Biology
Date 1999 May 20
PMID 10331254
Citations 65
Authors
Affiliations
Soon will be listed here.
Abstract

Buchnera, the bacterial endosymbionts of aphids, undergo severe population bottlenecks during maternal transmission through their hosts. Previous studies suggest an increased effect of drift within these strictly asexual, small populations, resulting in an increased fixation of slightly deleterious mutations. This study further explores sequence evolution in Buchnera using three approaches. First, patterns of codon usage were compared across several homologous Escherichia coli and Buchnera loci, in order to test the prediction that selection for the use of optimal codons is less effective in small populations. A chi 2-based measure of codon bias was developed to adjust for the overall A + T richness of silent positions in the endosymbionts. In contrast to E. coli homologues, adaptive codon bias across Buchnera loci is markedly low, and patterns of codon usage lack a strong relationship with gene expression level. These data suggest that codon usage in Buchnera has been shaped largely by mutational pressure and drift rather than by selection for translational efficiency. One exception to the overall lack of bias is groEL, which is known to be constitutively overexpressed in Buchnera and other endosymbionts. Second, relative-rate tests show elevated rates of sequence evolution of numerous protein-coding loci across Buchnera, compared to E. coli. Finally, consistently higher ratios of nonsynonymous to synonymous substitutions in Buchnera loci relative to the enteric bacteria strongly suggest the accumulation of nonsynonymous substitutions in endosymbiont lineages. Combined, these results suggest a decreased effectiveness of purifying selection in purging endosymbiont populations of slightly deleterious mutations, particularly those affecting codon usage and amino acid identity.

Citing Articles

A new lysine biosynthetic enzyme from a bacterial endosymbiont shaped by genetic drift and genome reduction.

Gilkes J, Frampton R, Board A, Hudson A, Price T, Morris V Protein Sci. 2024; 33(7):e5083.

PMID: 38924211 PMC: 11201819. DOI: 10.1002/pro.5083.


Comparative genomic analysis of symbiotic and free-living strains provides insights into the evolutionary origins of obligate -bacterial endosymbioses.

Wang R, Meng Q, Wang X, Xiao Y, Sun R, Zhang Z Appl Environ Microbiol. 2024; 90(3):e0190023.

PMID: 38334408 PMC: 10952467. DOI: 10.1128/aem.01900-23.


Coordination of host and endosymbiont gene expression governs endosymbiont growth and elimination in the cereal weevil Sitophilus spp.

Galvao Ferrarini M, Vallier A, Vincent-Monegat C, DellAglio E, Gillet B, Hughes S Microbiome. 2023; 11(1):274.

PMID: 38087390 PMC: 10717185. DOI: 10.1186/s40168-023-01714-8.


Selective advantages favour high genomic AT-contents in intracellular elements.

Dietel A, Merker H, Kaltenpoth M, Kost C PLoS Genet. 2019; 15(4):e1007778.

PMID: 31034469 PMC: 6519830. DOI: 10.1371/journal.pgen.1007778.


Evolution of the Natural Transformation Protein, ComEC, in Bacteria.

Pimentel Z, Zhang Y Front Microbiol. 2019; 9:2980.

PMID: 30627116 PMC: 6299819. DOI: 10.3389/fmicb.2018.02980.