TY - JOUR
T1 - Paramecium Genetics, Genomics, and Evolution
AU - Long, Hongan
AU - Johri, Parul
AU - Gout, Jean Francois
AU - Ni, Jiahao
AU - Hao, Yue
AU - Licknack, Timothy
AU - Wang, Yaohai
AU - Pan, Jiao
AU - Jiménez-Marín, Berenice
AU - Lynch, Michael
N1 - Publisher Copyright: Copyright © 2023 by the author(s).
PY - 2023/11/27
Y1 - 2023/11/27
N2 - The ciliate genus Paramecium served as one of the first model systems in microbial eukaryotic genetics, contributing much to the early understand-ing of phenomena as diverse as genome rearrangement, cryptic speciation, cytoplasmic inheritance, and endosymbiosis, as well as more recently to the evolution of mating types, introns, and roles of small RNAs in DNA processing. Substantial progress has recently been made in the area of com-parative and population genomics. Paramecium species combine some of the lowest known mutation rates with some of the largest known effective populations, along with likely very high recombination rates, thereby har-boring a population-genetic environment that promotes an exceptionally efficient capacity for selection. As a consequence, the genomes are extraordi-narily streamlined, with very small intergenic regions combined with small numbers of tiny introns. The subject of the bulk of Paramecium research, the ancient Paramecium aurelia species complex, is descended from two whole-genome duplication events that retain high degrees of synteny, thereby providing an ex-ceptional platform for studying the fates of duplicate genes. Despite having a common ancestor dating to several hundred million years ago, the known descendant species are morphologically indistinguishable, raising significant questions about the common view that gene duplications lead to the origins of evolutionary novelties.
AB - The ciliate genus Paramecium served as one of the first model systems in microbial eukaryotic genetics, contributing much to the early understand-ing of phenomena as diverse as genome rearrangement, cryptic speciation, cytoplasmic inheritance, and endosymbiosis, as well as more recently to the evolution of mating types, introns, and roles of small RNAs in DNA processing. Substantial progress has recently been made in the area of com-parative and population genomics. Paramecium species combine some of the lowest known mutation rates with some of the largest known effective populations, along with likely very high recombination rates, thereby har-boring a population-genetic environment that promotes an exceptionally efficient capacity for selection. As a consequence, the genomes are extraordi-narily streamlined, with very small intergenic regions combined with small numbers of tiny introns. The subject of the bulk of Paramecium research, the ancient Paramecium aurelia species complex, is descended from two whole-genome duplication events that retain high degrees of synteny, thereby providing an ex-ceptional platform for studying the fates of duplicate genes. Despite having a common ancestor dating to several hundred million years ago, the known descendant species are morphologically indistinguishable, raising significant questions about the common view that gene duplications lead to the origins of evolutionary novelties.
KW - Paramecium
KW - ciliates
KW - evolutionary cell biology
KW - gene duplication
KW - genome evolution
KW - population genomics
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U2 - 10.1146/annurev-genet-071819-104035
DO - 10.1146/annurev-genet-071819-104035
M3 - Review article
C2 - 38012024
SN - 0066-4197
VL - 57
SP - 391
EP - 410
JO - Annual review of genetics
JF - Annual review of genetics
ER -