scholarly journals Determining the interaction status and evolutionary fate of duplicated homomeric proteins

2020 ◽  
Vol 16 (8) ◽  
pp. e1008145
Author(s):  
Saurav Mallik ◽  
Dan S. Tawfik
Keyword(s):  
Author(s):  
Vera S. Bogdanova ◽  
Natalia V. Shatskaya ◽  
Anatoliy V. Mglinets ◽  
Oleg E. Kosterin ◽  
Gennadiy V. Vasiliev

AbstractPlastids and mitochondria have their own small genomes which do not undergo meiotic recombination and may have evolutionary fate different from each other and nuclear genome, thus highlighting interesting phenomena in plant evolution. We for the first time sequenced mitochondrial genomes of pea (Pisum L.), in 38 accessions mostly representing diverse wild germplasm from all over pea geographical range. Six structural types of pea mitochondrial genome were revealed. From the same accessions, plastid genomes were sequenced. Bayesian phylogenetic trees based on the plastid and mitochondrial genomes were compared. The topologies of these trees were highly discordant implying not less than six events of hybridisation of diverged wild peas in the past, with plastids and mitochondria differently inherited by the descendants. Such discordant inheritance of organelles is supposed to have been driven by plastid-nuclear incompatibility, known to be widespread in pea wide crosses and apparently shaping the organellar phylogenies. The topology of a phylogenetic tree based on the nucleotide sequence of a nuclear gene His5 coding for a histone H1 subtype corresponds to the current taxonomy and resembles that based on the plastid genome. Wild peas (Pisum sativum subsp. elatius s.l.) inhabiting Southern Europe were shown to be of hybrid origin resulting from crosses of peas similar to those presently inhabiting south-east and north-east Mediterranean in broad sense.


2020 ◽  
Vol 2 (7A) ◽  
Author(s):  
Rama Bhatia ◽  
Hande Kirit ◽  
Jonathan Bollback

The evolutionary fate of a horizontal gene transfer (HGT) event is determined by its fitness on the recipient cell, i.e., whether it is beneficial, neutral or deleterious. The distribution of fitness effects (DFE), thus is a fundamental predictor of the outcome of an HGT event. The environment plays a considerable role in determining the fitness cost of a horizontally transferred gene. We have studied the fitness effects of genes transferred from Salmonella enterica serovar Typhimurium to Escherichia coli in six environments, that potentially represent the conditions experienced by the two species. The data suggests high variability of genes in different environments. Genes, whose fitness varies substantially between environments, may be able to persist in populations while being deleterious in one environment, they may be neutral or even beneficial in another environment, suggesting that environmental fluctuations may increase the likelihood of HGT. In addition to the in vitro environments, we are also looking at, how changes in the intrinsic environment of a cell, after an HGT event, could affect fitness. An increase in protein dosage due to functional similarity of the horizontally transferred gene to the endogenous gene can cause an imbalance in the cell, thereby leading to a negative fitness effect. By comparing the growth rates of each ortholog gene with the wild type strain, we can elucidate when gene dosage acts as a barrier to HGT.


1991 ◽  
Vol 147 ◽  
pp. 93-99
Author(s):  
Sheo S. Prasad

Chemical considerations and simplified dynamical modeling suggest that dark cloud cores may be incessantly evolving such that the time spent at high core densities decreases as the density increases. After reaching a high density, gravitationally contracting dark cloud cores may either form stars or expand to states of lower densities. Cloud mass and initial density are amongst the factors that may control the evolutionary fate of the core. This view is diametrically opposite of the common belief that dense cores may be in near mechanical equilibrium. Mutually consistent end-to-end modeling of the spectral line profiles and intensities is needed to discern the reality.


2017 ◽  
Vol 154 (6) ◽  
pp. 1294-1305 ◽  
Author(s):  
JIAN HAN ◽  
YAOPING CAI ◽  
JAMES D. SCHIFFBAUER ◽  
HONG HUA ◽  
XING WANG ◽  
...  

AbstractThe earliest fossil record of animal biomineralization occurs in the latest Ediacaran Period (c. 550 Ma).CloudinaandSinotubulitesare two important tubular taxa among these earliest skeletal fossils. The evolutionary fate ofCloudina-type fossils across the Ediacaran–Cambrian transition, however, remains poorly understood. Here we report a multi-layered tubular microfossilFeiyanella manicagen. et sp. nov. from a phosphorite interval of the lowest Cambrian Kuanchuanpu Formation, southern Shaanxi Province, South China. This newly discovered fossil is a conical tube with a ‘funnel-in-funnel’ construction, showing profound morphological similarities toCloudinaandConotubus. On the other hand, the outer few layers, and particularly the outermost layer, ofFeiyanellatubes are regularly to irregularly corrugated, a feature strikingly similar to the variably folded/wrinkled tube walls ofSinotubulites. TheFeiyanellatubes additionally exhibit two orders of dichotomous branching, similar to branching structures reported occasionally inCloudinaand possibly indicative of asexual reproduction. Owing to broad similarities in tube morphology, tube wall construction and features presumably indicative of asexual reproduction,Cloudina, Conotubus, Sinotubulitesand the here describedFeiyanellamay thus constitute a monophyletic group traversing the Ediacaran–Cambrian boundary. The tube construction and palaeoecological strategy ofFeiyanellaputatively indicate evolutionary continuity in morphology and palaeoecology of benthic metazoan communities across the Ediacaran–Cambrian transition.


2014 ◽  
Vol 106 (2) ◽  
pp. 657a
Author(s):  
Amy I. Gilson ◽  
Eugene I. Shakhnovich
Keyword(s):  

2017 ◽  
Vol 27 (2) ◽  
pp. 493-507 ◽  
Author(s):  
Pascal Milesi ◽  
Benoît S. Assogba ◽  
Célestine M. Atyame ◽  
Nicolas Pocquet ◽  
Arnaud Berthomieu ◽  
...  

2006 ◽  
Vol 103 (9) ◽  
pp. 3220-3225 ◽  
Author(s):  
N. Vinckenbosch ◽  
I. Dupanloup ◽  
H. Kaessmann

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