scholarly journals On the Tetraploid Origin of the Maize Genome

2004 ◽  
Vol 5 (3) ◽  
pp. 281-284 ◽  
Author(s):  
Zuzana Swigonova ◽  
Jinsheng Lai ◽  
Jianxin Ma ◽  
Wusirika Ramakrishna ◽  
Victor Llaca ◽  
...  

Data from cytological and genetic mapping studies suggest that maize arose as a tetraploid. Two previous studies investigating the most likely mode of maize origin arrived at different conclusions. Gaut and Doebley [7] proposed a segmental allotetraploid origin of the maize genome and estimated that the two maize progenitors diverged at 20.5 million years ago (mya). In a similar study, using larger data set, Brendel and colleagues (quoted in [8]) suggested a single genome duplication at 16 mya. One of the key components of such analyses is to examine sequence divergence among strictly orthologous genes. In order to identify such genes, Lai and colleagues [10] sequenced five duplicated chromosomal regions from the maize genome and the orthologous counterparts from the sorghum genome. They also identified the orthologous regions in rice. Using positional information of genetic components, they identified 11 orthologous genes across the two duplicated regions of maize, and the sorghum and rice regions. Swigonovaet al. [12] analyzed the 11 orthologues, and showed that all five maize chromosomal regions duplicated at the same time, supporting a tetraploid origin of maize, and that the two maize progenitors diverged from each other at about the same time as each of them diverged from sorghum, about 11.9 mya.

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Guillermo Barturen ◽  
Stefanie Geisen ◽  
Francisco Dios ◽  
E. J. Maarten Hamberg ◽  
Michael Hackenberg ◽  
...  

Hypomethylated, CpG-rich DNA segments (CpG islands, CGIs) are epigenome markers involved in key biological processes. Aberrant methylation is implicated in the appearance of several disorders as cancer, immunodeficiency, or centromere instability. Furthermore, methylation differences at promoter regions between human and chimpanzee strongly associate with genes involved in neurological/psychological disorders and cancers. Therefore, the evolutionary comparative analyses of CGIs can provide insights on the functional role of these epigenome markers in both health and disease. Given the lack of specific tools, we developedCpGislandEVO. Briefly, we first compile a database of statistically significant CGIs for the best assembled mammalian genome sequences available to date. Second, by means of a coupled browser front-end, we focus on the CGIs overlapping orthologous genes extracted fromOrthoDB, thus ensuring the comparison between CGIs located on truly homologous genome segments. This allows comparing the main compositional features between homologous CGIs. Finally, to facilitate nucleotide comparisons, we lifted genome coordinates between assemblies from different species, which enables the analysis of sequence divergence by direct count of nucleotide substitutions and indels occurring between homologous CGIs. The resultingCpGislandEVOdatabase, linking together CGIs and single-cytosine DNA methylation data from several mammalian species, is freely available at our website.


PeerJ ◽  
2016 ◽  
Vol 4 ◽  
pp. e2627 ◽  
Author(s):  
Jean-Simon Brouard ◽  
Monique Turmel ◽  
Christian Otis ◽  
Claude Lemieux

BackgroundThe chloroplast genome sustained extensive changes in architecture during the evolution of the Chlorophyceae, a morphologically and ecologically diverse class of green algae belonging to the Chlorophyta; however, the forces driving these changes are poorly understood. The five orders recognized in the Chlorophyceae form two major clades: the CS clade consisting of the Chlamydomonadales and Sphaeropleales, and the OCC clade consisting of the Oedogoniales, Chaetophorales, and Chaetopeltidales. In the OCC clade, considerable variations in chloroplast DNA (cpDNA) structure, size, gene order, and intron content have been observed. The large inverted repeat (IR), an ancestral feature characteristic of most green plants, is present inOedogonium cardiacum(Oedogoniales) but is lacking in the examined members of the Chaetophorales and Chaetopeltidales. Remarkably, theOedogonium35.5-kb IR houses genes that were putatively acquired through horizontal DNA transfer. To better understand the dynamics of chloroplast genome evolution in the Oedogoniales, we analyzed the cpDNA of a second representative of this order,Oedocladium carolinianum.MethodsTheOedocladiumcpDNA was sequenced and annotated. The evolutionary distances separatingOedocladiumandOedogoniumcpDNAs and two other pairs of chlorophycean cpDNAs were estimated using a 61-gene data set. Phylogenetic analysis of an alignment of group IIA introns from members of the OCC clade was performed. Secondary structures and insertion sites of oedogonialean group IIA introns were analyzed.ResultsThe 204,438-bpOedocladiumgenome is 7.9 kb larger than theOedogoniumgenome, but its repertoire of conserved genes is remarkably similar and gene order differs by only one reversal. Although the 23.7-kb IR is missing the putative foreign genes found inOedogonium, it contains sequences coding for a putative phage or bacterial DNA primase and a hypothetical protein. Intergenic sequences are 1.5-fold longer and dispersed repeats are more abundant, but a smaller fraction of theOedocladiumgenome is occupied by introns. Six additional group II introns are present, five of which lack ORFs and carry highly similar sequences to that of the ORF-less IIA intron shared withOedogonium. Secondary structure analysis of the group IIA introns disclosed marked differences in the exon-binding sites; however, each intron showed perfect or nearly perfect base pairing interactions with its target site.DiscussionOur results suggest that chloroplast genes rearrange more slowly in the Oedogoniales than in the Chaetophorales and raise questions as to what was the nature of the foreign coding sequences in the IR of the common ancestor of the Oedogoniales. They provide the first evidence for intragenomic proliferation of group IIA introns in the Viridiplantae, revealing that intron spread in theOedocladiumlineage likely occurred by retrohoming after sequence divergence of the exon-binding sites.


The Auk ◽  
2001 ◽  
Vol 118 (4) ◽  
pp. 849-863 ◽  
Author(s):  
Jeremy J. Kirchman ◽  
Shannon J. Hackett ◽  
Steven M. Goodman ◽  
John M. Bates ◽  
R. Prum

Abstract We studied relationships of five extant members of the endemic Malagasy family Brachypteraciidae, the ground rollers, using several mitochondrial genes (cytochrome-b, NADH dehydrogenase 2, 12S ribosomal RNA, and cytochrome oxidase I). As outgroups, we used other coraciiforms including the Cuckoo Roller (Family Leptosomatidae, Leptosomus discolor), several true rollers (Corcaciidae) and a tody (Todidae). Partial sequences of the Long-tailed Ground Roller (Uratelornis chimaera) were obtained from toe pad samples taken off museum specimens. For a combined data set of all genes, Kimura two-parameter distances between sequences of the five ground roller species were high, averaging 11% divergence. For several species, samples were available from widely separated geographic regions and intraspecific sequence divergence was low (≤0.8%). Unweighted and weighted parsimony and maximum-likelihood analyses consistently recovered monophyly of the family, a sister relationship between Brachypteraciidae and Coraciidae, and monophyly of one of three currently recognized ground roller genera (Atelornis). At the base of the Brachypteraciidae clade, we could not fully resolve relationships between Uratelornis and two species currently placed in Brachypteracias. Because of the uncertainty of basal nodes in our phylogenetic reconstructions, we recommend returning B. squamigera to the monotypic genus Geobiastes. High levels of divergence among ground rollers are similar to levels found in other avian groups endemic to Madagascar. However, we suggest that molecular divergences appear far too low to be consistent with mid-Eocene fossils attributed to the family.


2014 ◽  
Vol 281 (1777) ◽  
pp. 20132174 ◽  
Author(s):  
Kevin P. Johnson ◽  
Julie M. Allen ◽  
Brett P. Olds ◽  
Lawrence Mugisha ◽  
David L. Reed ◽  
...  

The rate of DNA mutation and divergence is highly variable across the tree of life. However, the reasons underlying this variation are not well understood. Comparing the rates of genetic changes between hosts and parasite lineages that diverged at the same time is one way to begin to understand differences in genetic mutation and substitution rates. Such studies have indicated that the rate of genetic divergence in parasites is often faster than that of their hosts when comparing single genes. However, the variation in this relative rate of molecular evolution across different genes in the genome is unknown. We compared the rate of DNA sequence divergence between humans, chimpanzees and their ectoparasitic lice for 1534 protein-coding genes across their genomes. The rate of DNA substitution in these orthologous genes was on average 14 times faster for lice than for humans and chimpanzees. In addition, these rates were positively correlated across genes. Because this correlation only occurred for substitutions that changed the amino acid, this pattern is probably produced by similar functional constraints across the same genes in humans, chimpanzees and their ectoparasites.


Author(s):  
Wagner Hugo Bonat

Abstract: We present a general statistical modelling framework for handling multivariate mixed types of outcomes in the context of quantitative genetic analysis. The models are based on the multivariate covariance generalized linear models, where the matrix linear predictor is composed of an identity matrix combined with a relatedness matrix defined by a pedigree, representing the environmental and genetic components, respectively. We also propose a new index of heritability for non-Gaussian data. A case study on house sparrow (Passer domesticus) population with continuous, binomial and count outcomes is employed to motivate the new model. Simulation of multivariate marginal models is not trivial, thus we adapt the NORTA (Normal to anything) algorithm for simulation of multivariate covariance generalized linear models in the context of genetic data analysis. A simulation study is presented to assess the asymptotic properties of the estimating function estimators for the correlation between outcomes and the new heritability index parameters. The data set and R code are available in the supplementary material.


2019 ◽  
Vol 37 (1) ◽  
pp. 260-279 ◽  
Author(s):  
Carina F Mugal ◽  
Verena E Kutschera ◽  
Fidel Botero-Castro ◽  
Jochen B W Wolf ◽  
Ingemar Kaj

Abstract The ratio of nonsynonymous over synonymous sequence divergence, dN/dS, is a widely used estimate of the nonsynonymous over synonymous fixation rate ratio ω, which measures the extent to which natural selection modulates protein sequence evolution. Its computation is based on a phylogenetic approach and computes sequence divergence of protein-coding DNA between species, traditionally using a single representative DNA sequence per species. This approach ignores the presence of polymorphisms and relies on the indirect assumption that new mutations fix instantaneously, an assumption which is generally violated and reasonable only for distantly related species. The violation of the underlying assumption leads to a time-dependence of sequence divergence, and biased estimates of ω in particular for closely related species, where the contribution of ancestral and lineage-specific polymorphisms to sequence divergence is substantial. We here use a time-dependent Poisson random field model to derive an analytical expression of dN/dS as a function of divergence time and sample size. We then extend our framework to the estimation of the proportion of adaptive protein evolution α. This mathematical treatment enables us to show that the joint usage of polymorphism and divergence data can assist the inference of selection for closely related species. Moreover, our analytical results provide the basis for a protocol for the estimation of ω and α for closely related species. We illustrate the performance of this protocol by studying a population data set of four corvid species, which involves the estimation of ω and α at different time-scales and for several choices of sample sizes.


2020 ◽  
Vol 49 (D1) ◽  
pp. D274-D281 ◽  
Author(s):  
Michael Y Galperin ◽  
Yuri I Wolf ◽  
Kira S Makarova ◽  
Roberto Vera Alvarez ◽  
David Landsman ◽  
...  

Abstract The Clusters of Orthologous Genes (COG) database, also referred to as the Clusters of Orthologous Groups of proteins, was created in 1997 and went through several rounds of updates, most recently, in 2014. The current update, available at https://www.ncbi.nlm.nih.gov/research/COG, substantially expands the scope of the database to include complete genomes of 1187 bacteria and 122 archaea, typically, with a single genome per genus. In addition, the current version of the COGs includes the following new features: (i) the recently deprecated NCBI’s gene index (gi) numbers for the encoded proteins are replaced with stable RefSeq or GenBank\ENA\DDBJ coding sequence (CDS) accession numbers; (ii) COG annotations are updated for >200 newly characterized protein families with corresponding references and PDB links, where available; (iii) lists of COGs grouped by pathways and functional systems are added; (iv) 266 new COGs for proteins involved in CRISPR-Cas immunity, sporulation in Firmicutes and photosynthesis in cyanobacteria are included; and (v) the database is made available as a web page, in addition to FTP. The current release includes 4877 COGs. Future plans include further expansion of the COG collection by adding archaeal COGs (arCOGs), splitting the COGs containing multiple paralogs, and continued refinement of COG annotations.


The Auk ◽  
2000 ◽  
Vol 117 (2) ◽  
pp. 355-365 ◽  
Author(s):  
Beth Slikas ◽  
Isaac B. Jones ◽  
Scott R. Derrickson ◽  
Robert C. Fleischer

Abstract Using mitochondrial sequence data, we estimated phylogenetic relationships and genetic divergence among selected species of white-eyes (Zosteropidae). We focused on taxa endemic to islands in Micronesia, specifically Zosterops conspicillatus, Z. semperi, Z. hypolais, Rukia oleaginea, and Cleptornis marchei. We also included in our data set five additional species of Zosterops from the Indo-Australian region and three species from Africa, as well as additional passerine outgroups. Our mitochondrial sequence data revealed substantial genetic divergence (5.7 to 7.3%) among Z. conspicillatus, Z. semperi, and Z. hypolais, three taxa that formerly were treated as a single species. In addition, a sequence divergence of 6.5 ± SE of 1.7% was found between the population of Z. conspicillatus from Rota and “conspecific” populations on Guam, Tinian, and Saipan. The distinctiveness of the Rota population suggests that this taxon should be recognized as a distinct species, a result that bears on the conservation of this population because it has been declining dramatically in recent years. All optimal trees based on analysis of the mitochondrial sequence data place Rukia oleaginea within the genus Zosterops. In all optimal trees, Cleptornis marchei positions as the sister taxon to a clade including all other zosteropids included in this study. The trees based on our data strongly contradict the traditional classification of Cleptornis as a honeyeater (family Meliphagidae). Our data cannot resolve with any confidence the sister relationships of the insular endemic white-eyes, although the optimal trees suggest multiple colonizations of Micronesia by more than one white-eye lineage.


2021 ◽  
Author(s):  
Alec Brown ◽  
Matthew E Mead ◽  
Jacob L. Steenwyk ◽  
Gustavo Goldman ◽  
Antonis Rokas

Invasive aspergillosis is a deadly fungal disease; more than 400,000 patients are infected worldwide each year and the mortality rate can be as high as 50-95%. Of the ~450 species in the genus Aspergillus only a few are known to be clinically relevant, with the major pathogen Aspergillus fumigatus being responsible for ~50% of all invasive mold infections. Genomic comparisons of A. fumigatu to other Aspergillus species have historically focused on protein-coding regions. However, most A. fumigatus genes, including those that modulate its virulence, are also present in non-pathogenic close relatives of A. fumigatus. Our hypothesis is that differential gene regulation - mediated through the non-coding regions upstream of genes' transcription start sites - contributes to A. fumigatus pathogenicity. To begin testing this, we compared non-coding regions up to 500 base pairs upstream of the first codon of single-copy orthologous genes from the two A. fumigatus reference strains Af293 and A1163 and eight closely related Aspergillus section Fumigati species. We found that non-coding regions showed extensive sequence variation and lack of homology across species. By examining the evolutionary rates of both protein-coding and non-coding regions in a subset of orthologous genes with highly conserved non-coding regions across the phylogeny, we identified 418 genes, including 25 genes known to modulate A. fumigatus virulence, whose non-coding regions exhibit a different rate of evolution in A. fumigatus. Examination of sequence alignments of these non-coding regions revealed numerous instances of insertions, deletions, and other types of mutations of at least a few nucleotides in A. fumigatus compared to its close relatives. These results show that closely related Aspergillus species that vary greatly in their pathogenicity exhibit extensive non-coding sequence variation and identify numerous changes in non-coding regions of A. fumigatus genes known to contribute to virulence.


2009 ◽  
Vol 100 (3) ◽  
pp. 263-272 ◽  
Author(s):  
A. Skoracka ◽  
M. Dabert

AbstractThe cereal rust mite Abacarus hystrix (Nalepa), a significant pest of grasses, has been regarded as one of a few exceptions among eriophyoid mites with reference to the pattern of host plant utilization. At least 60 grass species have been recorded as its hosts. Thus, the mite has long been considered as a host generalist in which host specialization would not be likely to evolve. However, recent studies have revealed that host-associated specialization is possible in A. hystrix. Here, we aimed to discriminate between the three populations of A. hystrix associated with the different hosts (namely quackgrass, ryegrass and smooth brome) on the basis of mitochondrial (COI) and nuclear (D2 region of 28S rDNA) DNA sequences. The phylogenetic trees obtained with the maximum likelihood analysis of both COI and D2 region data sets showed that host-adapted strains of A. hystrix form distinct clades. Furthermore, on the COI nucleotide tree, the quackgrass- and brome-associated strains were internally divided each into two well-supported monophyletic clusters. The nucleotide D2 region data set tree showed that brome-associated strain is polyphyletic in origin. There is clear co-variation of DNA results with earlier morphological and ecological traits, as well as the results of crossing experiments. We showed that reproductively incompatible strains of A. hystrix exhibit more than 20% sequence divergence in the COI gene and 0.2% sequence divergence in the D2 28S rDNA. Our results did not confirm the placement of three host-associated strains of A. hystrix within one, ostensibly generalist, species.


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