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A genetic polymorphism evolving in parallel in two cell compartments and in two clades

BACKGROUND: The enzyme phosphoenolpyruvate carboxykinase, PEPCK, occurs in its guanosine-nucleotide-using form in animals and a few prokaryotes. We study its natural genetic variation in Colias (Lepidoptera, Pieridae). PEPCK offers a route, alternative to pyruvate kinase, for carbon skeletons to mov...

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Autores principales: Watt, Ward B, Hudson, Richard R, Wang, Baiqing, Wang, Eddie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556304/
https://www.ncbi.nlm.nih.gov/pubmed/23311980
http://dx.doi.org/10.1186/1471-2148-13-9
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author Watt, Ward B
Hudson, Richard R
Wang, Baiqing
Wang, Eddie
author_facet Watt, Ward B
Hudson, Richard R
Wang, Baiqing
Wang, Eddie
author_sort Watt, Ward B
collection PubMed
description BACKGROUND: The enzyme phosphoenolpyruvate carboxykinase, PEPCK, occurs in its guanosine-nucleotide-using form in animals and a few prokaryotes. We study its natural genetic variation in Colias (Lepidoptera, Pieridae). PEPCK offers a route, alternative to pyruvate kinase, for carbon skeletons to move between cytosolic glycolysis and mitochondrial Krebs cycle reactions. RESULTS: PEPCK is expressed in both cytosol and mitochondrion, but differently in diverse animal clades. In vertebrates and independently in Drosophila, compartment-specific paralogous genes occur. In a contrasting expression strategy, compartment-specific PEPCKs of Colias and of the silkmoth, Bombyx, differ only in their first, 5(′), exons; these are alternatively spliced onto a common series of following exons. In two Colias species from distinct clades, PEPCK sequence is highly variable at nonsynonymous and synonymous sites, mainly in its common exons. Three major amino acid polymorphisms, Gly 335 ↔ Ser, Asp 503 ↔ Glu, and Ile 629 ↔ Val occur in both species, and in the first two cases are similar in frequency between species. Homology-based structural modelling shows that the variants can alter hydrogen bonding, salt bridging, or van der Waals interactions of amino acid side chains, locally or at one another(′)s sites which are distant in PEPCK(′)s structure, and thus may affect its enzyme function. We ask, using coalescent simulations, if these polymorphisms(′) cross-species similarities are compatible with neutral evolution by genetic drift, but find the probability of this null hypothesis is 0.001 ≤ P ≤ 0.006 under differing scenarios. CONCLUSION: Our results make the null hypothesis of neutrality of these PEPCK polymorphisms quite unlikely, but support an alternative hypothesis that they are maintained by natural selection in parallel in the two species. This alternative can now be justifiably tested further via studies of PEPCK genotypes(′) effects on function, organismal performance, and fitness. This case emphasizes the importance, for evolutionary insight, of studying gene-specific mechanisms affected by natural genetic variation as an essential complement to surveys of such variation.
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spelling pubmed-35563042013-01-30 A genetic polymorphism evolving in parallel in two cell compartments and in two clades Watt, Ward B Hudson, Richard R Wang, Baiqing Wang, Eddie BMC Evol Biol Research Article BACKGROUND: The enzyme phosphoenolpyruvate carboxykinase, PEPCK, occurs in its guanosine-nucleotide-using form in animals and a few prokaryotes. We study its natural genetic variation in Colias (Lepidoptera, Pieridae). PEPCK offers a route, alternative to pyruvate kinase, for carbon skeletons to move between cytosolic glycolysis and mitochondrial Krebs cycle reactions. RESULTS: PEPCK is expressed in both cytosol and mitochondrion, but differently in diverse animal clades. In vertebrates and independently in Drosophila, compartment-specific paralogous genes occur. In a contrasting expression strategy, compartment-specific PEPCKs of Colias and of the silkmoth, Bombyx, differ only in their first, 5(′), exons; these are alternatively spliced onto a common series of following exons. In two Colias species from distinct clades, PEPCK sequence is highly variable at nonsynonymous and synonymous sites, mainly in its common exons. Three major amino acid polymorphisms, Gly 335 ↔ Ser, Asp 503 ↔ Glu, and Ile 629 ↔ Val occur in both species, and in the first two cases are similar in frequency between species. Homology-based structural modelling shows that the variants can alter hydrogen bonding, salt bridging, or van der Waals interactions of amino acid side chains, locally or at one another(′)s sites which are distant in PEPCK(′)s structure, and thus may affect its enzyme function. We ask, using coalescent simulations, if these polymorphisms(′) cross-species similarities are compatible with neutral evolution by genetic drift, but find the probability of this null hypothesis is 0.001 ≤ P ≤ 0.006 under differing scenarios. CONCLUSION: Our results make the null hypothesis of neutrality of these PEPCK polymorphisms quite unlikely, but support an alternative hypothesis that they are maintained by natural selection in parallel in the two species. This alternative can now be justifiably tested further via studies of PEPCK genotypes(′) effects on function, organismal performance, and fitness. This case emphasizes the importance, for evolutionary insight, of studying gene-specific mechanisms affected by natural genetic variation as an essential complement to surveys of such variation. BioMed Central 2013-01-12 /pmc/articles/PMC3556304/ /pubmed/23311980 http://dx.doi.org/10.1186/1471-2148-13-9 Text en Copyright ©2013 Watt et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Watt, Ward B
Hudson, Richard R
Wang, Baiqing
Wang, Eddie
A genetic polymorphism evolving in parallel in two cell compartments and in two clades
title A genetic polymorphism evolving in parallel in two cell compartments and in two clades
title_full A genetic polymorphism evolving in parallel in two cell compartments and in two clades
title_fullStr A genetic polymorphism evolving in parallel in two cell compartments and in two clades
title_full_unstemmed A genetic polymorphism evolving in parallel in two cell compartments and in two clades
title_short A genetic polymorphism evolving in parallel in two cell compartments and in two clades
title_sort genetic polymorphism evolving in parallel in two cell compartments and in two clades
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556304/
https://www.ncbi.nlm.nih.gov/pubmed/23311980
http://dx.doi.org/10.1186/1471-2148-13-9
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