Global gene expression patterns of grass carp following compensatory growth

被引:35
作者
He, Libo [1 ]
Pei, Yongyan [1 ,2 ]
Jiang, Yao [1 ,2 ]
Li, Yongming [1 ]
Liao, Lanjie [1 ]
Zhu, Zuoyan [1 ]
Wang, Yaping [1 ]
机构
[1] Chinese Acad Sci, Inst Hydrobiol, State Key Lab Freshwater Ecol & Biotechnol, Wuhan 430072, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
来源
BMC GENOMICS | 2015年 / 16卷
基金
中国国家自然科学基金;
关键词
Grass carp; Compensatory growth; Transcriptome analysis; RNA sequencing; Fasting; Re-feeding; Differentially expressed genes; RNA-SEQ; MOLECULAR CHARACTERIZATION; BINDING-PROTEIN; UBIQUITIN LIGASE; FACTOR-I; INSULIN; MUSCLE; MYOSIN; IDENTIFICATION; ACTIVATION;
D O I
10.1186/s12864-015-1427-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Compensatory growth is accelerated compared with normal growth and occurs when growth-limiting conditions are overcome. Most animals, especially fish, are capable of compensatory growth, but the mechanisms remain unclear. Further investigation of the mechanism of compensatory growth in fish is needed to improve feeding efficiency, reduce cost, and explore growth-related genes. Results: In the study, grass carp, an important farmed fish in China, were subjected to a compensatory growth experiment followed by transcriptome analysis by RNA-sequencing. Samples of fish from starved and re-feeding conditions were compared with the control. Under starved conditions, 4061 and 1988 differentially expressed genes (DEGs) were detected in muscle and liver tissue when compared the experimental group with control group, respectively. After re-feeding, 349 and 247 DEGs were identified in muscle and liver when the two groups were compared. Moreover, when samples from experimental group in starved and re-feeding conditions were compared, 4903 and 2444 DEGs were found in muscle and liver. Most of these DEGs were involved in metabolic processes, or encoded enzymes or proteins with catalytic activity or binding functions, or involved in metabolic and biosynthetic pathways. A number of the more significant DEGs were subjected to further analysis. Under fasting conditions, many up-regulated genes were associated with protein ubiquitination or degradation, whereas many down-regulated genes were involved in the metabolism of glucose and fatty acids. Under re-feeding conditions, genes participating in muscle synthesis and fatty acid metabolism were up-regulated significantly, and genes related to protein ubiquitination or degradation were down-regulated. Moreover, Several DEGs were random selected for confirmation by real-time quantitative PCR. Conclusions: Global gene expression patterns of grass carp during compensatory growth were determined. To our knowledge, this is a first reported for a teleost fish. The results will enhance our understanding of the mechanism of compensatory growth in teleost fish.
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页数:18
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