bioRxiv Science⌕ Search

Biology subjects

Ochoa-Ochoa, L. M.

Publications and source records attributed to Ochoa-Ochoa, L. M..

3 recordsLinked to original sources

Whole-genome analyses point to new candidate genes underlying aestivation in amphibians

When amphibians invaded the terrestrial realm, a strategy such as aestivation may have helped them to survive water and oxygen stress in the novel environment. In fact, aestivation appears to be an ancestral state in amphibians. We conducted a literature review about the genes previously linked to aestivation and then we searched for additional candidate genes related to the aestivation phenotype by comparing evolutionary rates of 13,578 genes in 31 amphibian species, including 10 aestivating species and 21 non-aestivating species. Based on the assumption that aestivation has two main requirements - a) metabolic regulation needed to control transitions to/from dormancy, and b) cell preservation strategies needed to sustain biological processes over long-term dormancy - we expected to find distinct relative evolutionary rates (RER) in genes related to those traits. We identified 323 genes with accelerated or decelerated RERs; these genes were enriched for some processes overlapping with our predictions and with literature findings, such as different modes of ATP production. Other genes related to protein and membrane trafficking (TRAPP, SNARE, and Arp2/3 protein complexes) are newly associated with aestivation. RER patterns suggest that aestivation in amphibians relies on a set of highly conserved core processes and other auxiliary processes that have diversified across the phylogeny. Given the vast number and diversity of aestivating amphibian lineages, we predict that more in-depth molecular studies of amphibian aestivation will offer novel insight into hypometabolic processes that could inspire medical innovations to prevent organ atrophy, address problems with angiogenesis, and combat processes underlying cancer.

evolutionary biology↗

Slowing down: A macroevolutionary approach to the hypometabolic strategies of amphibians

The ability to survive harsh environmental conditions has probably been a key factor in the evolutionary success of organisms that cannot migrate long distances, such as amphibians. We expect that having a hypometabolic strategy (HS) --aestivation or hibernation-- to deal with severe climates, would be a plesiomorphic trait. We 1) inferred the ancestral state of a HS, using two phylogenies for amphibians, 2) tested if species with a HS have larger distributional ranges, and 3) explored how a HS may affect amphibian assemblage resilience using multiple models of climate change. Ancestral state reconstruction for the most recent common ancestor (MRCA) of Class Amphibia showed [~]50% probability of a HS. The probability was higher for the MRCA of each Order (>70%), suggesting a widespread HS in the ancestors of modern amphibians. Phylogenetic regressions showed no relation between the probability of having a HS and the distribution range size. Climate analyses predict that tropical zones will have the greatest change in climate, involving novel harsh seasonality. Since tropical amphibian assemblages have the lowest proportion of species with HS, they may be more vulnerable to climate change. It is probable that HS have been key for the evolutionary success in amphibians, and they will likely impact their future survival in the face of climate change. Despite the potential importance of the HS for amphibians, information was available for a diverse but only a small subset of species; we urge researchers to report data on aestivation or hibernation in amphibians to facilitate future studies.

evolutionary biology↗

Concordant yet unique neutral and adaptive genomic responses to anthropogenically modified landscapes in Rhinella horribilis

Anthropized environments are significantly challenging for wild species. Rapid adaptation to such habitats is thus key for their long-term persistence. Deciphering the environmental factors associated with species tolerance to modified habitats is fundamental for understanding the genetic and connectivity patterns of individuals and the local adaptation of their populations. We studied the Giant Toad, Rhinella horribilis, from two landscapes with distinct levels of anthropogenic habitat modification, assessed their genomic diversity, structure and connectivity with ddRAD-seq genomic data, identified potential outlier loci and their relationship with environmental and physicochemical water variables, and evaluated if populations from the two study sites showed signals of parallel adaptation. Both concordant and unique patterns were found regarding landscape factors and genotype-environment associations related with the degree of anthropic modification between landscapes. Genomic structure and connectivity were significantly associated with the presence of temporary water bodies, low vegetation cover, high humidity, solar radiation, and temperature. Notably, we identified both shared and distinct outlier SNPs and annotated functional genes for the two landscapes. Genes were enriched for biological processes and metabolic pathways, which were in turn correlated with environmental and physicochemical water variables. Genes and metabolic pathways were associated mainly with embryonic development, sexual maturation and immune responses. Studies such as this one, in an often-disregarded species, illustrate how parallel and un-parallel adaptive landscape genomic patterns arise in the stressful conditions of anthropized habitats.

evolutionary biology↗