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Biology subjects

Morran, L. T.

Publications and source records attributed to Morran, L. T..

3 recordsLinked to original sources

Reduced signatures of gene duplication and non-random gene organization in shaping stage-specific patterns of gene expression across a relatively simple life cycle

Complex eukaryotes generally experience some degree of ecological transition as they develop, which is usually accompanied by the expression of different traits across their ontogeny. Theory suggests the evolution of differentiation between life stages is facilitated by the expression of different genes at different points throughout ontogeny, which alleviates pleiotropic evolutionary constraints. Therefore, ascertaining what contributes to specialized patterns of gene expression across ontogeny is fundamental to understanding the evolution of ontogenetic complexity. Expression divergence between duplicate genes and gene organization on chromosomes have been identified as important features of relatively complex ontogenies. Therefore, one could predict that their link to transcriptional specialization across ontogeny may be weaker in relatively simpler life cycles. Here, we investigated the links between gene duplication, gene organization, and stage-specific patterns of expression across the relatively simple Caenorhabditis elegans life cycle. We found that signatures of stage-biased chromosomal regions were weaker in C. elegans than what has been previously described in organisms with more complex ontogenies. Furthermore, we found the extent that duplicate genes varied in ontogenetic expression pattern was more constrained in C. elegans. Overall, our findings add to a body of evidence that suggests a link between gene duplication and gene organization and the evolution of complex ontogenies.

evolutionary biology↗

Evaluating the role of coevolution in a horizontally transmitted mutualism

Mutualism depends on the alignment of host and symbiont fitness. Horizontal transmission can readily decouple fitness interests, yet horizontally transmitted mutualisms are common in nature. We hypothesized that pairwise coevolution and specialization in host-symbiont interactions underlies the maintenance of cooperation in a horizontally transmitted mutualism. Alternatively, we predicted selection by multiple host species may select for cooperative traits in a generalist symbiont through diffuse coevolution. We tested for signatures of pairwise coevolutionary change between the squash bug Anasa tristis and its horizontally acquired bacterial symbiont Caballeronia spp. by measuring local adaptation. We found no evidence for local adaptation between sympatric combinations of A. tristis squash bugs and Caballeronia spp. across their native geographic range. To test for diffuse coevolution, we performed reciprocal inoculations to test for specialization between three Anasa host species and Caballeronia spp. symbionts isolated from conspecific hosts. We observed no evidence of specialization across host species. Our results demonstrate generalist dynamics underlie the interaction between Anasa insect hosts and their Caballeronia spp. symbionts. Specifically, diffuse coevolution between multiple host species with a shared generalist symbiont may maintain cooperative traits despite horizontal transmission.

evolutionary biology↗

The evolution of parasite host range in genetically diverse host populations

Parasites vary enormously in their host range. Why are some parasites specialists and others generalists? We tested the hypothesis that genetically diverse host populations select for parasites with broader host ranges than genetically homogeneous host populations. To do so, we selected for increased killing ability of the bacterial parasite Serratia marcescens in populations of the host Caenorhabditis elegans that were either diverse (50% mix of genotypes N2 and LTM1) or homogenous (100% N2 or LTM1). We found mixed support for the hypothesis. After 20 generations of selection, parasites selected in diverse host populations maintained a broad host range, as shown by the retention of high killing ability of a novel host genotype. Parasites selected in diverse populations killed N2 hosts equally well as parasites selected in homogenous populations of N2. However, N2-selected parasites lost killing ability against the novel host, consistent with the evolution of narrow host ranges in homogenous environments. In contrast, parasites selected in homogenous LTM1 populations did not specialize: they did not increase in their killing ability on LTM1 and did not lose killing ability against the novel host. Our results argue that the evolution of host range depends upon both the identity and diversity of hosts that a parasite encounters.

evolutionary biology↗