The genomic landscape underlying phenotypic integrity in the face of gene flow in crows

The role of interspecific gene flow in species diversification has long been debated and is increasingly appreciated. However, the effect of gene introgression on phenotypic divergences and genome heterogeneity remain unclear in case of early speciation. To investigate these questions Poelstra and colleagues studied the hybrid zone between the all-black carrion crows (Corvus corone) and the gray-coated hooded crows (C. cornix). Indeed, the absence of neutral genetic diversity between these two species and successful back-crossing of hybrids strongly contrast with the plumage coloration polymorphism that remained stable in natural populations. Moreover, colour assortative mating has been observed suggesting a prezygotic isolation and ongoing speciation. To investigate the causes of this stable phenotypes the authors first analysed the effect of gene flow on genome heterogeneity and then tried to link the observed gene flow heterogeneity with gene expression and phenotypes. Genetic differentiation between hooded and carrion crows First, they assembled and annotated a high-quality reference genome of one hooded male crow and identified 20’794 protein-coding genes. This reference genome was then used to aligned 60 genomes of unrelated individuals from two populations of carrion and two populations of hooded crows (Fig. 1). They identified 8.44 million of SNPs among which 5.27 …

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Evolution at two levels of gene expression in yeast

Protein abundances mainly determined by the balance of transcriptional and translational regulation. Because of the limited technology for the translational research, however, gene expression evolution was based almost entirely on studies of transcriptional regulation. With the quickly development of ribosome profiling–isolating and sequencing short fragments of mRNA bound by actively translating ribosomes–now we can study translational regulation conveniently and efficiently. Simultaneous detection of regulatory divergence at two levels In this paper, firstly, in order to assess the relative contributions of regulatory elements evolution to the changes in mRNA abundance and translation rate, the authors applied ribosome profiling and RNAseq to two species of Saccharomyces yeast (S. cerevisiae and  S. paradoxus )and their interspecific hybrid (figure 1). Within hybrids, both alleles share the same trans-acting cellular environment. Therefore, different mRNA abundance or translation efficiency is caused by cis-regulatory divergence. By applied these methods, the authors showed cis-regulatory divergence in both transcription and translation are abundant, almost 35% orthologs have significant divergence in translational efficiency, as compared with 61% with significant divergence in mRNA abundance. Because they identified cis-regulatory elements change at two regulatory levels simultaneously, an interesting question will be asked is whether changes at the two levels could be reinforcing (acting at the same direction) or opposing (acting in opposite directions). Compared …

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Convergent evolution of the genomes of marine mammals

Convergent evolution is defined by the independent evolution of similar traits in different lineages, in order to adapt to similar environmental conditions. Examples of this phenomenon include adaptations to altitude in humans, independent evolution of flight in birds and bats or the multiple evolution of C4 carbon fixation in plants. Yet, the molecular bases of convergent evolution are often lacking. In this paper, authors shed light on the genomic basis of a classical example of convergent evolution, the adaptation to marine life. Mammals evolved multiple independent times to inhabit the marine environment (Fig 1). Species from three different clades share similar phenotypic adaptations involved in communication, locomotion, thermal regulation, buoyancy… Cetaceans (whales and dolphins) and sirenians (manatees) emerged during the Eocene while pinnipeds (walruses) appeared during Miocene. In this paper, Foote and colleagues investigated the convergent evolution of the genomes of marine mammals at two levels. First, they sought for protein coding genes evolving under positive selection across the three lineages. Second, they studied the convergence of amino acid substitutions within these positively selected genes. Detection of protein coding genes under positive selection The authors performed de novo assembly of the genomes of killer whale, manatee and walrus and completed …

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The African Genome Variation Project shapes medical genetics in Africa.

  Despite being the world’s most genetically diverse continent, only a handful of studies attempted to understand the genetic risks for diseases of the African populations. This study shines light not only on the genetic diversity to help learn more about the variants that are associated with malaria and hypertension, but also on the population history across sub-Saharan African populations. Beside the comprehensive map of the African variants obtained from genotypes of 1,481 individuals and whole-genome sequences of 320 individuals, authors offered a design of the array suitable to capturing variants of African populations. Summary and comments of the paper Population structure in SSA. Comparing ~2.2 million variants of 18 ethno-linguistic groups from sub-Saharan Africa (SSA), authors found modest differentiation among SSA populations (mean pairwise Fst = 0.019) and among Niger-Congo language groups (mean pairwise Fst = 0.009). In the article, authors suggested that the modest differentiation among Niger-Congo language group showed evidence for ‘Bantu expansion’. However, the Fig1.a shows sample distribution mostly next to the Western, East and South African coasts, rather then inside of continent where the Bantu expansion occurred, therefore indicating the sampling bias. Furthermore, the authors found a high proportion of unshared and novel variants in …

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The genetics of monarch butterfly migration and warning colouration

The monarch butterfly (Danaus plexippus) has a large distribution worldwide. It occurs in North, Central, and South America, Caribbean, and it has recently dispersed to other locations, such as Oceania and Africa. Two traits of this butterfly are incredibly intriguing: their annual migration in North America, and their warning coloration. Among the populations spread out around the globe, only the population of North America has a migrant behavior. Monarchs migrate thousands of kilometers from northern United States and southern Canada to overwinter in Mexico. In Spring, they begin mating and flying back to the North. This long annual migration process happens throughout the life time of more than one generation. Regarding their warning coloration, what is intriguing about it is the occurrence of an intense polymorphism in this trait when compared to other butterflies of the same genus. Monarchs and other Danaus butterflies have by default bright orange wings. This bold coloration warns predators about their toxicity. However, in a monarch population from Hawaii, some butterflies have white instead of orange wings. In this paper, authors investigate, through comparative population genomics, the genetic base for such migration and color polymorphisms of the monarch butterfly. The migration of the monarchs By …

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Gibbon genome and the fast karyotype evolution of small apes

All contents refer to the original paper (Carbone et al. Nature. 2014 Sep 11;513(7517):195-201) Summary and personal comments This paper concerns a study of gibbon karyotype in the perspective of their divergent evolution from ancestral primates. Gibbons, small monkeys living in South-East Asia, differ from other primates, such as great apes and Old World monkeys, for a surprising number of chromosomal rearrangements. The authors aimed to study the mechanisms underlying such an important plasticity in gibbon genome gibbon. 1) The authors sequenced and assembled the genome of a white-cheeked gibbon female (Nomascus leucogenys), ordered in 26 chromosomes (against human reference), and analyzed gibbon-human synteny breakpoints (= rupture of synteny=physical co-localization of genetic loci on the same chromosome within gibbon and human). Fig 2a shows Oxford plots for human (axys y) versus other primates chromosomes (axys x), expressed in terms of collinear blocks of > 10 Mb. It is evident from the graphic that, when compared to other primates, gibbons present the highest rate of chromosome rearrangements, graphically visualized as a scattered instead of a linear plot (Fig2a), in particular large-scale reshuffling (as shown in Fig 2b, right part of the graphic). Examples of synteny breakpoints, such as chromosomal inversion, are shown in …

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The genetics of Mexico recapitulates Native American substructure and affects biomedical traits

Mexico, hosted many cultures such as the Olmec, the Toltec, the Maya and the Aztec, conquered and colonized by the Spanish Empire in 1521. The country harbors a large source of pre-Columbian diversity and their genetic contributions to today’s population. In a recent paper, Moreno-Estrada et al. 2014 performed a detailed genetic study of Mexican genetic diversity. The results showed the genetic stratification among indigenous populations and an association between subcontinental ancestry and lung function. In the first part of the study, to estimate the genetic diversity, researchers examined autosomal single-nucleotide polymorphisms for more than 500 Native Mexican individuals from all around Mexico. Statistical analysis of genomic data showed that some populations within Mexico are more differentiated than European and East Asian populations. This extreme differentiation thought to be a result of isolation followed by a bottleneck and small effective population sizes. The data was analyzed in various ways (ROH and IBD analysis, PCA etc.) and revealed the population substructure of Mexico. In all of the analysis, the results confirmed that Seri (northernmost) and Lacandon (southernmost) have the highest level of differentiation. Also, the differentiation between Seri and Lacandon was greater than average differentiation between human populations. The relationships between …

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Gibbon genome and the fast karyotype evolution of small apes

Gibbons are small apes living in southeast Asia that diverged between Old Monkeys and great apes and whose most distinctive feature is the high rate of evolutionary chromosomal rearrangement. The aim of this study was threefold: First, the authors looked into the mechanisms that could explain the extraordinary rate of chromosomal rearrangement of gibbons. Second, they explored their evolutionary history to shed light into the timing and order of splitting of the gibbon genera. Third, they looked into the functional evolution of genes that might be associated with gibbon-specific adaptations. To do so, they sequenced and assembled the genome of the white-cheeked gibbon (Nomascus leucogenys), showing that the quality and statistics of the assembled genome was comparable to that of other primates (Table 1 and Fig.S1).   Chromosomal rearrangement and LAVA insertions Chromosomal rearrangement was confirmed by comparing the karyotype of the assembled Gibbon genome (Nleu1.0) to that of human. Figure 2A shows the extraordinarily high number of rearrangements compared to other primates. Furthermore these reshuffling events affect long stretches of chromosomes (displayed in Fig.2A are collinear blocks larger than 10Mb), whereas short-scale rearrangement events occur at levels comparable to other primates (Fig.2B). Since the four Gibbon genera of this …

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Electrogenic fish – what’s in charge of the charge?

Electric organs – organs that are capable of creating and discharging electricity – have evolved independently in at least six different lineages of fish (Torpediniformes, Rajiformes, Mormyroidea, Euteleostei, Siluriformes, Gymnotiformes) and play an important role in communication, navigation, defense and predation. To investigate whether the convergent evolution of these organs has a common genetic basis, Jason Gallant and his coworkers studied the transcriptome of five species of electrogenic fish in three different lineages: Electrophorus electricus, Sternopygus macrurus, Eigenmannia virescens (Gymnotiforme), Malapterurus electricus (Siluriforme) and Brienomyrus brachyistius (Mormyroidea). Electric organs are comprised of arrays of electrocytes – asymmetric cells that are enriched in cation-specific ion channels on one and sodium pumps on the opposing side. The resulting ion flux slowly charges the electrocyte membrane and upon activation by a neuronal stimulus, the voltage is discharged, generating an electrical pulse from the fish. Although the morphology of electric organs and electrocytes varies substantially amongst these species, they are all muscle-derived tissue and originate developmentally from muscle progenitor cells. Since this evolution of muscular to electrogenic tissue has occurred several times independently, the authors investigated, whether the underlying genetic mechanisms are shared. To address this question, Gallant et al. first sequenced and assembled …

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Population Genomics Reveal Recent Speciation and Rapid Evolutionary Adaptation in Polar Bears

The polar bear (Ursus maritimus) is a carnivorous species which is closely related to the brown bear (Ursus arctos) and is adapted to the severe living conditions of the High Arctic due to the great physiological changes happened during evolutionary speciation. Despite numerous researches it is still unclear when exactly this two species diverged. That’s why, Liu with colleagues in their work tried to determine a reliable divergence time of polar bear and brown bear populations and investigated demographic history as well as selection and adaptation of polar bears. Summary By applying a population genomic framework the authors analyzed 89 complete nuclear genomes of polar bears and brown bears. They showed that two species diverged 479-343 thousand years ago (kya) and found 16 genes under strong positive selection on the polar bear in comparison with the brown bear. They analyzed more precisely nine of these genes that are known to be associated with high risk of cardiomyopathy and vascular diseases in humans. However, in polar bears these genes are responsible for an important reorganization of the cardiovascular system which allowed them to survive in extreme life’s conditions within Arctic Circle (e.g. very low temperatures, high physical activity in cold water, high …

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