Distinct expression profiles of LncRNAs between brown adipose tissue and skeletal muscle

•Expression profiles of LncRNAs between brown adipose tissue and skeletal muscle.•704 up-regulated and 896 down-regulated lncRNAs were identified.•Analysis of dysregulated LncRNAs.•AK003288 may affect energy metabolism.•Find new therapeutic target for combatting obesity. Both brown adipose tissue an...

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Veröffentlicht in:Biochemical and biophysical research communications 2014-01, Vol.443 (3), p.1028-1034
Hauptverfasser: Zhang, Jun, Cui, Xianwei, Shen, Yahui, Pang, Lingxia, Zhang, Aiqing, Fu, Ziyi, Chen, Jiantao, Guo, Xirong, Gan, Weihua, Ji, Chenbo
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container_issue 3
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container_title Biochemical and biophysical research communications
container_volume 443
creator Zhang, Jun
Cui, Xianwei
Shen, Yahui
Pang, Lingxia
Zhang, Aiqing
Fu, Ziyi
Chen, Jiantao
Guo, Xirong
Gan, Weihua
Ji, Chenbo
description •Expression profiles of LncRNAs between brown adipose tissue and skeletal muscle.•704 up-regulated and 896 down-regulated lncRNAs were identified.•Analysis of dysregulated LncRNAs.•AK003288 may affect energy metabolism.•Find new therapeutic target for combatting obesity. Both brown adipose tissue and skeletalmuscle have abundant mitochondria and energy consumption capacity. They are similar in origin and gain different potential of energy metabolism after differentiation and maturation. The mechanism that cause the difference is not yet fully understood. Long non-coding RNAs (lncRNAs) which comprise the bulk of the human non-coding transcriptome have been proved to play key roles in various biological processes. Whether they will have a function on the differentiation and energy metabolism between BAT and skeletalmuscle is still unknown. To identify the cellular long noncoding RNAs (lncRNAs) involved in the progress, we used the next generation transcriptome sequencing and microarray techniques, and investigated 704 up-regulated and 896 down-regulated lncRNAs (fold-change >3.0) in BAT by comparing the expression profile. Furthermore, we reported AK003288 associated with junctophilin 2 (Jph2) gene which may affect energy metabolism. This study show distinct expression profiles of LncRNAs between brown adipose tissue and skeletal muscle which provide information for further research on differentiation of adipocyte and transdifferentiation between BAT and skeletalmuscle that will be helpful to find a new therapeutic target for combatting obesity.
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Both brown adipose tissue and skeletalmuscle have abundant mitochondria and energy consumption capacity. They are similar in origin and gain different potential of energy metabolism after differentiation and maturation. The mechanism that cause the difference is not yet fully understood. Long non-coding RNAs (lncRNAs) which comprise the bulk of the human non-coding transcriptome have been proved to play key roles in various biological processes. Whether they will have a function on the differentiation and energy metabolism between BAT and skeletalmuscle is still unknown. To identify the cellular long noncoding RNAs (lncRNAs) involved in the progress, we used the next generation transcriptome sequencing and microarray techniques, and investigated 704 up-regulated and 896 down-regulated lncRNAs (fold-change &gt;3.0) in BAT by comparing the expression profile. Furthermore, we reported AK003288 associated with junctophilin 2 (Jph2) gene which may affect energy metabolism. 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Both brown adipose tissue and skeletalmuscle have abundant mitochondria and energy consumption capacity. They are similar in origin and gain different potential of energy metabolism after differentiation and maturation. The mechanism that cause the difference is not yet fully understood. Long non-coding RNAs (lncRNAs) which comprise the bulk of the human non-coding transcriptome have been proved to play key roles in various biological processes. Whether they will have a function on the differentiation and energy metabolism between BAT and skeletalmuscle is still unknown. To identify the cellular long noncoding RNAs (lncRNAs) involved in the progress, we used the next generation transcriptome sequencing and microarray techniques, and investigated 704 up-regulated and 896 down-regulated lncRNAs (fold-change &gt;3.0) in BAT by comparing the expression profile. Furthermore, we reported AK003288 associated with junctophilin 2 (Jph2) gene which may affect energy metabolism. 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Both brown adipose tissue and skeletalmuscle have abundant mitochondria and energy consumption capacity. They are similar in origin and gain different potential of energy metabolism after differentiation and maturation. The mechanism that cause the difference is not yet fully understood. Long non-coding RNAs (lncRNAs) which comprise the bulk of the human non-coding transcriptome have been proved to play key roles in various biological processes. Whether they will have a function on the differentiation and energy metabolism between BAT and skeletalmuscle is still unknown. To identify the cellular long noncoding RNAs (lncRNAs) involved in the progress, we used the next generation transcriptome sequencing and microarray techniques, and investigated 704 up-regulated and 896 down-regulated lncRNAs (fold-change &gt;3.0) in BAT by comparing the expression profile. Furthermore, we reported AK003288 associated with junctophilin 2 (Jph2) gene which may affect energy metabolism. 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subjects Adipose Tissue, Brown - metabolism
Animals
Brown adipose tissue
Computational Biology
Gene Expression Profiling
Gene Expression Regulation
Gene Ontology
Humans
Long non-coding RNA
Mice
Mice, Inbred C57BL
Microarray
Muscle, Skeletal - metabolism
Oligonucleotide Array Sequence Analysis
Real-Time Polymerase Chain Reaction
RNA, Long Noncoding - genetics
RNA, Long Noncoding - metabolism
Signal Transduction - genetics
Skeletal muscle
title Distinct expression profiles of LncRNAs between brown adipose tissue and skeletal muscle
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