scholarly journals Inferences on the Evolutionary History of theDrosophila americanaPolymorphicX/4Fusion From Patterns of Polymorphism at theX-LinkedparalyticandelavGenes

Genetics ◽  
2003 ◽  
Vol 164 (4) ◽  
pp. 1459-1469 ◽  
Author(s):  
Cristina P Vieira ◽  
Paula A Coelho ◽  
Jorge Vieira

AbstractIn Drosophila there is limited evidence on the nature of evolutionary forces affecting chromosomal arrangements other than inversions. The study of the X/4 fusion polymorphism of Drosophila americana is thus of interest. Polymorphism patterns at the paralytic (para) gene, located at the base of the X chromosome, suggest that there is suppressed crossing over in this region between fusion and nonfusion chromosomes but not within fusion and nonfusion chromosomes. These data are thus compatible with previous claims that within fusion chromosomes the amino acid clines found at fused1 (also located at the base of the X chromosome) are likely maintained by local selection. The para data set also suggests a young age of the X/4 fusion. Polymorphism data on para and elav (located at the middle region of the X chromosome) suggest that there is no population structure other than that caused by the X/4 fusion itself. These findings are therefore compatible with previous claims that selection maintains the strong association observed between the methionine/threonine variants at fused1 and the status of the X chromosome as fused or unfused to the fourth chromosome.

2017 ◽  
Vol 153 (1) ◽  
pp. 29-35 ◽  
Author(s):  
Anthony J. Tosi ◽  
Hirohisa Hirai

A representative of Cercopithecus erythrotis was surveyed at a 9.3-kb region of the X chromosome. The data were compared against homologous sequences of closely related Cercopithecus monkeys including C. cephus, a species recently shown to have 2 polymorphic X-chromosomal lineages. Direct sequence comparisons and subsequent phylogenetic analyses revealed that synapomorphies in the first 4.3 kb cluster C. erythrotis with one C. cephus lineage, while synapomorphies in the latter 5.0 kb join it with the second C. cephus lineage. This pattern very likely reflects an ancestral episode of introgression from C. cephus into C. erythrotis followed by a recombination event. Similar groups of synapomorphies occur at different phylogenetic depths within the C. erythrotis/C. cephus/C. ascanius radiation and reveal new details in the evolutionary history of this 3-species clade.


2010 ◽  
Vol 76 (6) ◽  
pp. 1913-1925 ◽  
Author(s):  
Ping Lang ◽  
Tristan Lefebure ◽  
Wei Wang ◽  
Paulina Pavinski Bitar ◽  
Richard J. Meinersmann ◽  
...  

ABSTRACT The purpose of this work was to evaluate the evolutionary history of Campylobacter coli isolates derived from multiple host sources and to use microarray comparative genomic hybridization to assess whether there are particular genes comprising the dispensable portion of the genome that are more commonly associated with certain host species. Genotyping and ClonalFrame analyses of an expanded 16-gene multilocus sequence typing (MLST) data set involving 85 isolates from 4 different hosts species tentatively supported the development of C. coli host-preferred groups and suggested that recombination has played various roles in their diversification; however, geography could not be excluded as a contributing factor underlying the history of some of the groups. Population genetic analyses of the C. coli pubMLST database by use of STRUCTURE suggested that isolates from swine form a relatively homogeneous genetic group, that chicken and human isolates show considerable genetic overlap, that isolates from ducks and wild birds have similarity with environmental water samples and that turkey isolates have a connection with human infection similar to that observed for chickens. Analysis of molecular variance (AMOVA) was performed on these same data and suggested that host species was a significant factor in explaining genetic variation and that macrogeography (North America, Europe, and the United Kingdom) was not. The microarray comparative genomic hybridization data suggested that there were combinations of genes more commonly associated with isolates derived from particular hosts and, combined with the results on evolutionary history, suggest that this is due to a combination of common ancestry in some cases and lateral gene transfer in others.


Having spent many years in working through the Cretaceous Cribrimorph material in the British Museum, and, consequently, the literature of the subject, I was forced to the conclusion that various Cribrimorph stocks had independently arisen over and over again from Membranimorph ancestors, had run through a more or less similar evolution, and, finally, become extinct; so that the many forms described under Cribrilina, Membraniporella , and other Recent genera were really in no way closely related to these, and the Cretaceous Cribrimorph forms, in consequence, needed at lea st a generic nomenclature of their own. These Cretaceous forms fell under ten main stocks, between which no direct relationship could be discovered, and whose common ancestor must be sought far back among the primitive Membranimorphs; so that it did not seem too much to claim for each of these main stocks the status of a family. Within certain families were several well-defined groups, which, nevertheless, in each case had features in common, rendering it possible for all to have been derived from a common Cribrimorph ancestor; it seem ed permissible, therefore, to regard these groups as subfamilies. Thus a complete evolutionary classification was drawn up for the Cretaceous Cribrimorphs, and this, in the tersest possible form, was published in the ‘Annals and Magazine of Natural History (Lang, 1916). Since the whole evolutionary scheme was implicit in the tabular analysis, it was hoped that this would be lucid enough to be acceptable without further explanation. From, various criticisms, it appears that this is not so, and the opportunity has been taken in this essay to select one subfamily and expand the condensed account into a fuller statement. The subfamily Pelmatoporinæ was chosen partly because of its large size, and partly because it illustrates so fully the principles of evolution exhibited by the Cretaceous Cribrimorphs generally; but other subfamilies would serve the same purpose nearly as well. The morphology of the group is the first consideration; and since it is founded on the structure of the species Pelmatopora calceata , which closely approximates to the supposed ancestral form, this radical species is considered in some detail. Then, after examining the evolutionary aim of Cretaceous Cribrimorphs as a whole, we are in a position to appreciate the general evolutionary history of each character of the radical species, as it proceeds from the less to the more complex forms in the several lineages. Next, peculiar modifications of certain characters are described, giving the criteria for generic distinctions; then the evolution of forms within each genus. The results are compared with those obtained by W. K. Spencer in his work on Cretaceous Asteroidea. Next, the stratigraphical distribution of the forms is examined to see how far this corroborates the relationships established on morphic evidence; and, finally, the evidence of recapitulation, as shown in the colonial development (Astogeny), is brought to bear in connection with the other two criteria of relationships already examined.


2019 ◽  
Author(s):  
Ryan Bracewell ◽  
Doris Bachtrog

The Drosophila obscura species group shows dramatic variation in karyotype, including transitions among sex chromosomes. Members of the affinis and pseudoobscura subgroups contain a neo-X chromosome (a fusion of the X with an autosome), and it was shown that ancestral Y genes of Drosophila have become autosomal in species that contain the neo-X. Detailed analysis in species of the pseudoobscura subgroup revealed a translocation of ancestral Y genes to the small dot chromosome of that group. Here, we show that the Y-dot translocation is restricted to the pseudoobscura subgroup, and translocation of Y genes in the affinis subgroup followed a different route. We find that most ancestral Y genes moved independently to autosomal or X-linked locations in different taxa of the affinis subgroup, and we propose a dynamic model of sex chromosome formation and turnover in the obscura species group. Our results show that Y genes can find unique paths to escape an unfavorable genomic environment.


2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Dario Karmeinski ◽  
Karen Meusemann ◽  
Jessica A. Goodheart ◽  
Michael Schroedl ◽  
Alexander Martynov ◽  
...  

Abstract Background The soft-bodied cladobranch sea slugs represent roughly half of the biodiversity of marine nudibranch molluscs on the planet. Despite their global distribution from shallow waters to the deep sea, from tropical into polar seas, and their important role in marine ecosystems and for humans (as targets for drug discovery), the evolutionary history of cladobranch sea slugs is not yet fully understood. Results To enlarge the current knowledge on the phylogenetic relationships, we generated new transcriptome data for 19 species of cladobranch sea slugs and two additional outgroup taxa (Berthella plumula and Polycera quadrilineata). We complemented our taxon sampling with previously published transcriptome data, resulting in a final data set covering 56 species from all but one accepted cladobranch superfamilies. We assembled all transcriptomes using six different assemblers, selecting those assemblies that provided the largest amount of potentially phylogenetically informative sites. Quality-driven compilation of data sets resulted in four different supermatrices: two with full coverage of genes per species (446 and 335 single-copy protein-coding genes, respectively) and two with a less stringent coverage (667 genes with 98.9% partition coverage and 1767 genes with 86% partition coverage, respectively). We used these supermatrices to infer statistically robust maximum-likelihood trees. All analyses, irrespective of the data set, indicate maximal statistical support for all major splits and phylogenetic relationships at the family level. Besides the questionable position of Noumeaella rubrofasciata, rendering the Facelinidae as polyphyletic, the only notable discordance between the inferred trees is the position of Embletonia pulchra. Extensive testing using Four-cluster Likelihood Mapping, Approximately Unbiased tests, and Quartet Scores revealed that its position is not due to any informative phylogenetic signal, but caused by confounding signal. Conclusions Our data matrices and the inferred trees can serve as a solid foundation for future work on the taxonomy and evolutionary history of Cladobranchia. The placement of E. pulchra, however, proves challenging, even with large data sets and various optimization strategies. Moreover, quartet mapping results show that confounding signal present in the data is sufficient to explain the inferred position of E. pulchra, again leaving its phylogenetic position as an enigma.


2020 ◽  
Vol 12 (2) ◽  
pp. 3878-3889 ◽  
Author(s):  
Eduard Ocaña-Pallarès ◽  
Zaida Vergara ◽  
Bénédicte Desvoyes ◽  
Manuel Tejada-Jimenez ◽  
Ainoa Romero-Jurado ◽  
...  

Abstract The conservation of orthologs of most subunits of the origin recognition complex (ORC) has served to propose that the whole complex is common to all eukaryotes. However, various uncertainties have arisen concerning ORC subunit composition in a variety of lineages. Also, it is unclear whether the ancestral diversification of ORC in eukaryotes was accompanied by the neofunctionalization of some subunits, for example, role of ORC1 in centriole homeostasis. We have addressed these questions by reconstructing the distribution and evolutionary history of ORC1-5/CDC6 in a taxon-rich eukaryotic data set. First, we identified ORC subunits previously undetected in divergent lineages, which allowed us to propose a series of parsimonious scenarios for the origin of this multiprotein complex. Contrary to previous expectations, we found a global tendency in eukaryotes to increase or decrease the number of subunits as a consequence of genome duplications or streamlining, respectively. Interestingly, parasites show significantly lower number of subunits than free-living eukaryotes, especially those with the lowest genome size and gene content metrics. We also investigated the evolutionary origin of the ORC1 role in centriole homeostasis mediated by the PACT region in human cells. In particular, we tested the consequences of reducing ORC1 levels in the centriole-containing green alga Chlamydomonas reinhardtii. We found that the proportion of centrioles to flagella and nuclei was not dramatically affected. This, together with the PACT region not being significantly more conserved in centriole-bearing eukaryotes, supports the notion that this neofunctionalization of ORC1 would be a recent acquisition rather than an ancestral eukaryotic feature.


2020 ◽  
Vol 37 (9) ◽  
pp. 2616-2629 ◽  
Author(s):  
Ming-Shan Wang ◽  
Sheng Wang ◽  
Yan Li ◽  
Yadvendradev Jhala ◽  
Mukesh Thakur ◽  
...  

Abstract Genetic introgression not only provides material for adaptive evolution but also confounds our understanding of evolutionary history. This is particularly true for canids, a species complex in which genome sequencing and analysis has revealed a complex history of admixture and introgression. Here, we sequence 19 new whole genomes from high-altitude Tibetan and Himalayan wolves and dogs and combine these into a larger data set of 166 whole canid genomes. Using these data, we explore the evolutionary history and adaptation of these and other canid lineages. We find that Tibetan and Himalayan wolves are closely related to each other, and that ∼39% of their nuclear genome is derived from an as-yet-unrecognized wolf-like lineage that is deeply diverged from living Holarctic wolves and dogs. The EPAS1 haplotype, which is present at high frequencies in Tibetan dog breeds and wolves and confers an adaptive advantage to animals living at high altitudes, was probably derived from this ancient lineage. Our study underscores the complexity of canid evolution and demonstrates how admixture and introgression can shape the evolutionary trajectories of species.


2019 ◽  
Vol 45 (6) ◽  
pp. 1119-1141
Author(s):  
Venla Oikkonen

The study of ancient DNA (aDNA) has gained increasing attention in science and society as a tool for tracing hominin evolution. While aDNA research overlaps with the history of population genetics, it embodies a specific configuration of technology, temporality, temperature, and place that, this article suggests, cannot be fully unpacked with existing science and technology studies approaches to population genetics. This article explores this configuration through the 2010 discovery of the Denisovan hominin based on aDNA retrieved from a finger bone and tooth in Siberia. The analysis explores how the Denisovan was enacted as a technoscientific object through the cool and even temperatures of Denisova Cave, assumptions about the connection between individual and population, the status of populations as evolutionary entities, and underlying colonialist and imperialist imaginaries of Siberia and Melanesia. The analysis sheds light on how aDNA research is changing the parameters within which evolutionary history is imagined and conceptualized. Through the case study, it also outlines some ways in which the specific technoscientific and cultural entanglements of aDNA can be critically explored.


2020 ◽  
Vol 12 (5) ◽  
pp. 494-505
Author(s):  
Ryan Bracewell ◽  
Doris Bachtrog

Abstract The Drosophila obscura species group shows dramatic variation in karyotype, including transitions among sex chromosomes. Members of the affinis and pseudoobscura subgroups contain a neo-X chromosome (a fusion of the X with an autosome), and ancestral Y genes have become autosomal in species harboring the neo-X. Detailed analysis of species in the pseudoobscura subgroup revealed that ancestral Y genes became autosomal through a translocation to the small dot chromosome. Here, we show that the Y-dot translocation is restricted to the pseudoobscura subgroup, and translocation of ancestral Y genes in the affinis subgroup likely followed a different route. We find that most ancestral Y genes have translocated to unique autosomal or X-linked locations in different taxa of the affinis subgroup, and we propose a dynamic model of sex chromosome formation and turnover in the obscura species group. Our results suggest that Y genes can find unique paths to escape unfavorable genomic environments that form after sex chromosome–autosome fusions.


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