Unique gene expression profile of the proliferating Xenopus tadpole tail blastema cells deciphered by RNA-sequencing analysis

Organ regenerative ability depends on the animal species and the developmental stage. The molecular bases for variable organ regenerative ability, however, remain unknown. Previous studies have identified genes preferentially expressed in the blastema tissues in various animals, but transcriptome an...

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Veröffentlicht in:PloS one 2015-03, Vol.10 (3), p.e0111655-e0111655
Hauptverfasser: Tsujioka, Hiroshi, Kunieda, Takekazu, Katou, Yuki, Shirahige, Katsuhiko, Kubo, Takeo
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Kunieda, Takekazu
Katou, Yuki
Shirahige, Katsuhiko
Kubo, Takeo
description Organ regenerative ability depends on the animal species and the developmental stage. The molecular bases for variable organ regenerative ability, however, remain unknown. Previous studies have identified genes preferentially expressed in the blastema tissues in various animals, but transcriptome analysis of the isolated proliferating blastema cells has not yet been reported. In the present study, we used RNA-sequencing analysis to analyze the gene expression profile of isolated proliferating blastema cells of regenerating Xenopus laevis tadpole tails. We used flow cytometry to isolate proliferating cells, and non-proliferating blastema cells, from regenerating tadpole tails as well as proliferating tail bud cells from tail bud embryos, the latter two of which were used as control cells, based on their DNA content. Among the 28 candidate genes identified by RNA-sequencing analysis, quantitative reverse transcription-polymerase chain reaction identified 10 genes whose expression was enriched in regenerating tadpole tails compared with non-regenerating tadpole tails or tails from the tail bud embryos. Among them, whole mount in situ hybridization revealed that chromosome segregation 1-like and interleukin 11 were expressed in the broad area of the tail blastema, while brevican, lysyl oxidase, and keratin 18 were mainly expressed in the notochord bud in regenerating tails. We further combined whole mount in situ hybridization with immunohistochemistry for the incorporated 5-bromo-2-deoxyuridine to confirm that keratin 18 and interleukin 11 were expressed in the proliferating tail blastema cells. Based on the proposed functions of their homologs in other animal species, these genes might have roles in the extracellular matrix formation in the notochord bud (brevican and lysyl oxidase), cell proliferation (chromosome segregation 1-like and keratin 18), and in the maintenance of the differentiation ability of proliferating blastema cells (interleukin 11) in regenerating tadpole tails.
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The molecular bases for variable organ regenerative ability, however, remain unknown. Previous studies have identified genes preferentially expressed in the blastema tissues in various animals, but transcriptome analysis of the isolated proliferating blastema cells has not yet been reported. In the present study, we used RNA-sequencing analysis to analyze the gene expression profile of isolated proliferating blastema cells of regenerating Xenopus laevis tadpole tails. We used flow cytometry to isolate proliferating cells, and non-proliferating blastema cells, from regenerating tadpole tails as well as proliferating tail bud cells from tail bud embryos, the latter two of which were used as control cells, based on their DNA content. Among the 28 candidate genes identified by RNA-sequencing analysis, quantitative reverse transcription-polymerase chain reaction identified 10 genes whose expression was enriched in regenerating tadpole tails compared with non-regenerating tadpole tails or tails from the tail bud embryos. Among them, whole mount in situ hybridization revealed that chromosome segregation 1-like and interleukin 11 were expressed in the broad area of the tail blastema, while brevican, lysyl oxidase, and keratin 18 were mainly expressed in the notochord bud in regenerating tails. We further combined whole mount in situ hybridization with immunohistochemistry for the incorporated 5-bromo-2-deoxyuridine to confirm that keratin 18 and interleukin 11 were expressed in the proliferating tail blastema cells. Based on the proposed functions of their homologs in other animal species, these genes might have roles in the extracellular matrix formation in the notochord bud (brevican and lysyl oxidase), cell proliferation (chromosome segregation 1-like and keratin 18), and in the maintenance of the differentiation ability of proliferating blastema cells (interleukin 11) in regenerating tadpole tails.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0111655</identifier><identifier>PMID: 25775398</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Amphibians ; Animal species ; Animals ; Antigens ; Cell growth ; Cell Proliferation ; Cytokines ; Cytometry ; Deoxyribonucleic acid ; Developmental stages ; DNA ; DNA sequencing ; Embryos ; Experiments ; Extracellular matrix ; Flow cytometry ; Frogs ; Gene expression ; Gene Expression Profiling ; Gene sequencing ; Genes ; Genetic research ; Homology ; Hybridization ; Immunohistochemistry ; Interleukin 11 ; Keratin ; Larva - cytology ; Larva - genetics ; Larva - physiology ; Lymphocytes ; Lysyl oxidase ; Notochord ; Oxidase ; Polymerase chain reaction ; Regeneration - genetics ; Reverse transcription ; Ribonucleic acid ; RNA ; Rodents ; Science ; Sequence Analysis, RNA ; Studies ; T cell receptors ; Tail - cytology ; Tails ; Tissue engineering ; Xenopus ; Xenopus laevis ; Xenopus laevis - genetics ; Xenopus laevis - physiology</subject><ispartof>PloS one, 2015-03, Vol.10 (3), p.e0111655-e0111655</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Tsujioka et al. 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The molecular bases for variable organ regenerative ability, however, remain unknown. Previous studies have identified genes preferentially expressed in the blastema tissues in various animals, but transcriptome analysis of the isolated proliferating blastema cells has not yet been reported. In the present study, we used RNA-sequencing analysis to analyze the gene expression profile of isolated proliferating blastema cells of regenerating Xenopus laevis tadpole tails. We used flow cytometry to isolate proliferating cells, and non-proliferating blastema cells, from regenerating tadpole tails as well as proliferating tail bud cells from tail bud embryos, the latter two of which were used as control cells, based on their DNA content. Among the 28 candidate genes identified by RNA-sequencing analysis, quantitative reverse transcription-polymerase chain reaction identified 10 genes whose expression was enriched in regenerating tadpole tails compared with non-regenerating tadpole tails or tails from the tail bud embryos. Among them, whole mount in situ hybridization revealed that chromosome segregation 1-like and interleukin 11 were expressed in the broad area of the tail blastema, while brevican, lysyl oxidase, and keratin 18 were mainly expressed in the notochord bud in regenerating tails. We further combined whole mount in situ hybridization with immunohistochemistry for the incorporated 5-bromo-2-deoxyuridine to confirm that keratin 18 and interleukin 11 were expressed in the proliferating tail blastema cells. Based on the proposed functions of their homologs in other animal species, these genes might have roles in the extracellular matrix formation in the notochord bud (brevican and lysyl oxidase), cell proliferation (chromosome segregation 1-like and keratin 18), and in the maintenance of the differentiation ability of proliferating blastema cells (interleukin 11) in regenerating tadpole tails.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25775398</pmid><doi>10.1371/journal.pone.0111655</doi><oa>free_for_read</oa></addata></record>
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subjects Amphibians
Animal species
Animals
Antigens
Cell growth
Cell Proliferation
Cytokines
Cytometry
Deoxyribonucleic acid
Developmental stages
DNA
DNA sequencing
Embryos
Experiments
Extracellular matrix
Flow cytometry
Frogs
Gene expression
Gene Expression Profiling
Gene sequencing
Genes
Genetic research
Homology
Hybridization
Immunohistochemistry
Interleukin 11
Keratin
Larva - cytology
Larva - genetics
Larva - physiology
Lymphocytes
Lysyl oxidase
Notochord
Oxidase
Polymerase chain reaction
Regeneration - genetics
Reverse transcription
Ribonucleic acid
RNA
Rodents
Science
Sequence Analysis, RNA
Studies
T cell receptors
Tail - cytology
Tails
Tissue engineering
Xenopus
Xenopus laevis
Xenopus laevis - genetics
Xenopus laevis - physiology
title Unique gene expression profile of the proliferating Xenopus tadpole tail blastema cells deciphered by RNA-sequencing analysis
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