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Title: Molecular mechanisms of extensive mitochondrial gene rearrangementin plethodontid salamanders

Journal Article · · Molecular Biology and Evolution

Extensive gene rearrangement is reported in the mitochondrial genomes of lungless salamanders (Plethodontidae). In each genome with a novel gene order, there is evidence that the rearrangement was mediated by duplication of part of the mitochondrial genome, including the presence of both pseudogenes and additional, presumably functional, copies of duplicated genes. All rearrangement-mediating duplications include either the origin of light strand replication and the nearby tRNA genes or the regions flanking the origin of heavy strand replication. The latter regions comprise nad6, trnE, cob, trnT, an intergenic spacer between trnT and trnP and, in some genomes, trnP, the control region, trnF, rrnS, trnV, rrnL, trnL1, and nad1. In some cases, two copies of duplicated genes, presumptive regulatory regions, and/or sequences with no assignable function have been retained in the genome following the initial duplication; in other genomes, only one of the duplicated copies has been retained. Both tandem and non-tandem duplications are present in these genomes, suggesting different duplication mechanisms. In some of these mtDNAs, up to 25 percent of the total length is composed of tandem duplications of non-coding sequence that includes putative regulatory regions and/or pseudogenes of tRNAs and protein-coding genes along with otherwise unassignable sequences. These data indicate that imprecise initiation and termination of replication, slipped-strand mispairing, and intra-molecular recombination may all have played a role in generating repeats during the evolutionary history of plethodontid mitochondrial genomes.

Research Organization:
Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
USDOE Director. Office of Science. Office of Biological andEnvironmental Research; National Science Foundation Fellowship, NationalScience Foundation doctoral dissertation improvement grant0105824,National Institutes of Health Grant, National Science FoundationAmphiliaTree Project EF-0334939
DOE Contract Number:
DE-AC02-05CH11231
OSTI ID:
860912
Report Number(s):
LBNL-58173; R&D Project: 626849; BnR: KP1103010; TRN: US200524%%365
Journal Information:
Molecular Biology and Evolution, Vol. 22; Related Information: Journal Publication Date: 2005
Country of Publication:
United States
Language:
English