Dietary and Flight Energetic Adaptations in a Salivary Gland Transcriptome of an Insectivorous Bat
We hypothesized that evolution of salivary gland secretory proteome has been important in adaptation to insectivory, the most common dietary strategy among Chiroptera. A submandibular salivary gland (SMG) transcriptome was sequenced for the little brown bat, Myotis lucifugus. The likely secretory pr...
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Published in | PloS one Vol. 9; no. 1; p. e83512 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
14.01.2014
Public Library of Science (PLoS) |
Subjects | |
Online Access | Get full text |
ISSN | 1932-6203 1932-6203 |
DOI | 10.1371/journal.pone.0083512 |
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Abstract | We hypothesized that evolution of salivary gland secretory proteome has been important in adaptation to insectivory, the most common dietary strategy among Chiroptera. A submandibular salivary gland (SMG) transcriptome was sequenced for the little brown bat, Myotis lucifugus. The likely secretory proteome of 23 genes included seven (RETNLB, PSAP, CLU, APOE, LCN2, C3, CEL) related to M. lucifugus insectivorous diet and metabolism. Six of the secretory proteins probably are endocrine, whereas one (CEL) most likely is exocrine. The encoded proteins are associated with lipid hydrolysis, regulation of lipid metabolism, lipid transport, and insulin resistance. They are capable of processing exogenous lipids for flight metabolism while foraging. Salivary carboxyl ester lipase (CEL) is thought to hydrolyze insect lipophorins, which probably are absorbed across the gastric mucosa during feeding. The other six proteins are predicted either to maintain these lipids at high blood concentrations or to facilitate transport and uptake by flight muscles. Expression of these seven genes and coordinated secretion from a single organ is novel to this insectivorous bat, and apparently has evolved through instances of gene duplication, gene recruitment, and nucleotide selection. Four of the recruited genes are single-copy in the Myotis genome, whereas three have undergone duplication(s) with two of these genes exhibiting evolutionary 'bursts' of duplication resulting in multiple paralogs. Evidence for episodic directional selection was found for six of seven genes, reinforcing the conclusion that the recruited genes have important roles in adaptation to insectivory and the metabolic demands of flight. Intragenic frequencies of mobile- element-like sequences differed from frequencies in the whole M. lucifugus genome. Differences among recruited genes imply separate evolutionary trajectories and that adaptation was not a single, coordinated event. |
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AbstractList | We hypothesized that evolution of salivary gland secretory proteome has been important in adaptation to insectivory, the most common dietary strategy among Chiroptera. A submandibular salivary gland (SMG) transcriptome was sequenced for the little brown bat, Myotis lucifugus. The likely secretory proteome of 23 genes included seven (RETNLB, PSAP, CLU, APOE, LCN2, C3, CEL) related to M. lucifugus insectivorous diet and metabolism. Six of the secretory proteins probably are endocrine, whereas one (CEL) most likely is exocrine. The encoded proteins are associated with lipid hydrolysis, regulation of lipid metabolism, lipid transport, and insulin resistance. They are capable of processing exogenous lipids for flight metabolism while foraging. Salivary carboxyl ester lipase (CEL) is thought to hydrolyze insect lipophorins, which probably are absorbed across the gastric mucosa during feeding. The other six proteins are predicted either to maintain these lipids at high blood concentrations or to facilitate transport and uptake by flight muscles. Expression of these seven genes and coordinated secretion from a single organ is novel to this insectivorous bat, and apparently has evolved through instances of gene duplication, gene recruitment, and nucleotide selection. Four of the recruited genes are single-copy in the Myotis genome, whereas three have undergone duplication(s) with two of these genes exhibiting evolutionary ‘bursts’ of duplication resulting in multiple paralogs. Evidence for episodic directional selection was found for six of seven genes, reinforcing the conclusion that the recruited genes have important roles in adaptation to insectivory and the metabolic demands of flight. Intragenic frequencies of mobile- element-like sequences differed from frequencies in the whole M. lucifugus genome. Differences among recruited genes imply separate evolutionary trajectories and that adaptation was not a single, coordinated event. We hypothesized that evolution of salivary gland secretory proteome has been important in adaptation to insectivory, the most common dietary strategy among Chiroptera. A submandibular salivary gland (SMG) transcriptome was sequenced for the little brown bat, Myotis lucifugus. The likely secretory proteome of 23 genes included seven (RETNLB, PSAP, CLU, APOE, LCN2, C3, CEL) related to M. lucifugus insectivorous diet and metabolism. Six of the secretory proteins probably are endocrine, whereas one (CEL) most likely is exocrine. The encoded proteins are associated with lipid hydrolysis, regulation of lipid metabolism, lipid transport, and insulin resistance. They are capable of processing exogenous lipids for flight metabolism while foraging. Salivary carboxyl ester lipase (CEL) is thought to hydrolyze insect lipophorins, which probably are absorbed across the gastric mucosa during feeding. The other six proteins are predicted either to maintain these lipids at high blood concentrations or to facilitate transport and uptake by flight muscles. Expression of these seven genes and coordinated secretion from a single organ is novel to this insectivorous bat, and apparently has evolved through instances of gene duplication, gene recruitment, and nucleotide selection. Four of the recruited genes are single-copy in the Myotis genome, whereas three have undergone duplication(s) with two of these genes exhibiting evolutionary 'bursts' of duplication resulting in multiple paralogs. Evidence for episodic directional selection was found for six of seven genes, reinforcing the conclusion that the recruited genes have important roles in adaptation to insectivory and the metabolic demands of flight. Intragenic frequencies of mobile- element-like sequences differed from frequencies in the whole M. lucifugus genome. Differences among recruited genes imply separate evolutionary trajectories and that adaptation was not a single, coordinated event.We hypothesized that evolution of salivary gland secretory proteome has been important in adaptation to insectivory, the most common dietary strategy among Chiroptera. A submandibular salivary gland (SMG) transcriptome was sequenced for the little brown bat, Myotis lucifugus. The likely secretory proteome of 23 genes included seven (RETNLB, PSAP, CLU, APOE, LCN2, C3, CEL) related to M. lucifugus insectivorous diet and metabolism. Six of the secretory proteins probably are endocrine, whereas one (CEL) most likely is exocrine. The encoded proteins are associated with lipid hydrolysis, regulation of lipid metabolism, lipid transport, and insulin resistance. They are capable of processing exogenous lipids for flight metabolism while foraging. Salivary carboxyl ester lipase (CEL) is thought to hydrolyze insect lipophorins, which probably are absorbed across the gastric mucosa during feeding. The other six proteins are predicted either to maintain these lipids at high blood concentrations or to facilitate transport and uptake by flight muscles. Expression of these seven genes and coordinated secretion from a single organ is novel to this insectivorous bat, and apparently has evolved through instances of gene duplication, gene recruitment, and nucleotide selection. Four of the recruited genes are single-copy in the Myotis genome, whereas three have undergone duplication(s) with two of these genes exhibiting evolutionary 'bursts' of duplication resulting in multiple paralogs. Evidence for episodic directional selection was found for six of seven genes, reinforcing the conclusion that the recruited genes have important roles in adaptation to insectivory and the metabolic demands of flight. Intragenic frequencies of mobile- element-like sequences differed from frequencies in the whole M. lucifugus genome. Differences among recruited genes imply separate evolutionary trajectories and that adaptation was not a single, coordinated event. |
Audience | Academic |
Author | Phillips, Carleton J. Lessa, Enrique P. Baker, Robert J. Tandler, Bernard Gannon, Michael R. Goecks, Jeremy Phillips, Caleb D. Sotero-Caio, Cibele G. |
AuthorAffiliation | 4 Departamento de Ecología y Evolución, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay 1 Department of Biological Sciences, Texas Tech University, Lubbock, Texas, United States of America Louisiana State University, United States of America 2 Department of Biology, Emory University, Atlanta, Georgia, United States of America 5 Department of Biological Sciences, School of Dental Medicine, Case Western Reserve University, Cleveland, Ohio, United States of America 3 Department of Math and Computer Science, Emory University, Atlanta, Georgia, United States of America 6 Department of Biology, Pennsylvania State University, Altoona College, Altoona, Pennsylvania, United States of America |
AuthorAffiliation_xml | – name: 2 Department of Biology, Emory University, Atlanta, Georgia, United States of America – name: 4 Departamento de Ecología y Evolución, Facultad de Ciencias, Universidad de la República, Montevideo, Uruguay – name: 6 Department of Biology, Pennsylvania State University, Altoona College, Altoona, Pennsylvania, United States of America – name: 3 Department of Math and Computer Science, Emory University, Atlanta, Georgia, United States of America – name: Louisiana State University, United States of America – name: 5 Department of Biological Sciences, School of Dental Medicine, Case Western Reserve University, Cleveland, Ohio, United States of America – name: 1 Department of Biological Sciences, Texas Tech University, Lubbock, Texas, United States of America |
Author_xml | – sequence: 1 givenname: Carleton J. surname: Phillips fullname: Phillips, Carleton J. – sequence: 2 givenname: Caleb D. surname: Phillips fullname: Phillips, Caleb D. – sequence: 3 givenname: Jeremy surname: Goecks fullname: Goecks, Jeremy – sequence: 4 givenname: Enrique P. surname: Lessa fullname: Lessa, Enrique P. – sequence: 5 givenname: Cibele G. surname: Sotero-Caio fullname: Sotero-Caio, Cibele G. – sequence: 6 givenname: Bernard surname: Tandler fullname: Tandler, Bernard – sequence: 7 givenname: Michael R. surname: Gannon fullname: Gannon, Michael R. – sequence: 8 givenname: Robert J. surname: Baker fullname: Baker, Robert J. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24454705$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1093_gbe_evaa151 crossref_primary_10_1093_icb_icx011 crossref_primary_10_1093_jmammal_gyaa149 crossref_primary_10_1093_gbe_evu204 crossref_primary_10_1093_nar_gkaa550 crossref_primary_10_1073_pnas_1814995116 crossref_primary_10_1073_pnas_2110647119 |
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Copyright | COPYRIGHT 2014 Public Library of Science 2014 Phillips et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2014 Phillips et al 2014 Phillips et al |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Competing Interests: The authors have declared that no competing interests exist. Conceived and designed the experiments: CJP RJB EPL. Performed the experiments: JG BT CDP CGS-C. Analyzed the data: CJP CDP CGS-C RJB. Contributed reagents/materials/analysis tools: BT JG MRG. Wrote the paper: CJP CDP BT RJB. Electron microscopy: BT. Bioinformatics: JG CDP CJP. Analysis of natural selection: EPL CDP. Moblile element: CJP CGS-C. |
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SubjectTerms | Adaptation Adaptation, Physiological - genetics Animal behavior Animals Apolipoprotein E Apolipoproteins Bats Bats (Animals) Bioinformatics Biological evolution Biological Transport Biology Chiroptera Chiroptera - genetics Chiroptera - metabolism Chiroptera - physiology Diet Dietary Fats - metabolism Energy Metabolism - genetics Enzymes Evolution Evolution, Molecular Flight Flight, Animal - physiology Forage Gastric mucosa Gene Dosage Gene Duplication Gene expression Gene sequencing Genes Genomes Genomics Histology Hydrolysis Hyperlipidemias - genetics Hypotheses Insects Insulin Insulin resistance Lipase Lipid metabolism Lipid Metabolism - genetics Lipids Mammals Metabolic syndrome Metabolism Morphology Muscles Myotis lucifugus Physiology Proteins Proteomes Proteomics Reproduction (copying) Rodents Salivary gland Secretion Submandibular Gland - metabolism Transcriptome Transport |
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Title | Dietary and Flight Energetic Adaptations in a Salivary Gland Transcriptome of an Insectivorous Bat |
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