猪Enho基因的分子克隆及其仔猪的组织分布

Molecular cloning, characterization and expression of the energy homeostasis-associated gene in piglet 猪 Enho 基因的分子克隆及其仔猪的组织分布 1 2 first-author 1 1 1 3 1 1 4 5 1 corresp ‡Corresponding Authors ‡Corresponding Authors †E-mail:zemengfeng2006@163.comfunfarm@126.com †E-mail:zemengfeng2006@163.comfunfarm@126.com zemengfeng2006@163.com 2 corresp ‡Corresponding Authors ‡Corresponding Authors †E-mail:zemengfeng2006@163.comfunfarm@126.com †E-mail:zemengfeng2006@163.comfunfarm@126.com zemengfeng2006@163.com Research Center of Healthy Breeding Livestock & Poultry, Hunan Engineering & Research Center of Animal & Poultry Science, Key Lab Agro-ecology Processing Subtropical Region, Scientific Observational and Experimental Station of Animal Nutrition and Feed Science in South-Central, Ministry of Agriculture, Institute of Subtropical Agriculture, Chinese Academy of Sciences, Changsha 410125, China Research Center of Healthy Breeding Livestock & Poultry, Hunan Engineering & Research Center of Animal & Poultry Science, Key Lab Agro-ecology Processing Subtropical Region, Scientific Observational and Experimental Station of Animal Nutrition and Feed Science in South-Central, Ministry of Agriculture, Institute of Subtropical Agriculture, Chinese Academy of Sciences, Changsha 410125, China Hunan Institute of Microbiology, Changsha 410009, China Hunan Institute of Microbiology, Changsha 410009, China Rice Research Institute of Sichuan Agricultural University, Chengdu 625014, China Rice Research Institute of Sichuan Agricultural University, Chengdu 625014, China Fujian Aonong Biotechnology Corporation, Xiamen 361007, China Fujian Aonong Biotechnology Corporation, Xiamen 361007, China Hubei Collaborative Innovation Center for Animal Nutrition and Feed Safety, Wuhan Polytechnic University, Wuhan 430023, China Hubei Collaborative Innovation Center for Animal Nutrition and Feed Safety, Wuhan Polytechnic University, Wuhan 430023, China The energy homeostasis-associated ( Enho ) gene encodes a secreted protein, adropin, which regulates the expression of hepatic lipogenic genes and adipose tissue peroxisome proliferator-activated receptor γ, a major regulator of lipogenesis. In the present study, the porcine ( Sus scrofa ) homologue of the Enho gene, which was named pEnho , was amplified by reverse transcriptase polymerase chain reaction (RT-PCR) using oligonucleotide primers derived from in silico sequences. The gene sequence was submitted into the GenBank of NCBI, and the access number is GQ414763. The pEnho encodes a protein of 76 amino acids which shows 75% similarity to Homo sapiens adropin. The expression profile of pEnho in tissues (liver, muscle, anterior jejunum, posterior jejunum, and ileum) was determined by quantitative real-time RT-PCR. pEnho was localized on porcine chromosome 10 and no introns were found. In conclusion, pEnho was cloned and analysed with the aim of increasing knowledge about glucose and lipid metabolism in piglets and helping to promote the health and growth of piglets through adropin regulation. 目的 2 通过 pEnho 基因的克隆，分析 pEnho 基因在仔猪相关组织的分布情况，增加仔猪糖脂代谢方面相关的知识，为通过调控adropin来促进仔猪的健康和生长提供理论基础。 创新点 2 首次克隆了猪 Enho 基因，命名为 pEnho ，其基因序列提交至美国国立生物技术信息中心（NCBI）（No.GQ414763）。 方法 2 通过实时荧光定量逆转录聚合酶链式反应（real-timeRT-PCR）方法获得猪Enho基因序列，并应用BLAST、ClustalW、PHYLIP、TMHMM、Helixturnhelix等生物信息学软件对其基因序列进行分析；通过荧光定量PCR方法检测了不同日龄（出生后1、7、14和21天）猪 Enho 基因的组织分布（肝脏、肌肉、空肠前端、空肠后端和回肠）。 结论 2 克隆得到 pEnho 基因序列；发现随着仔猪日龄的增加，其表达量有下降；在组织分布上，产后7天内pEnho在肠道（特别是回肠）的表达量较高，在第14天和第21天，各被检组织的表达量无显著差异。 Adropin Energy homeostasis-associated ( Enho ) gene Gene coloning Piglets RT-PCR Adropin Enho 基因克隆 仔猪 定量PCR Introduction 1 Adropin is a peptide hormone, which is encoded by the energy homeostasis-associated ( Enho ) gene, and is expressed differently in various tissues (Ganesh-Kumar et al., 2008 2008 ; Lovren et al., 2010 2010 ; Aydin et al., 2013a 2013a ; 2013b 2013b ; Kuloglu and Aydin, 2014 2014 ). The main function of adropin is to maintain energy homeostasis and insulin response (Ganesh-Kumar et al., 2008 2008 ). It has been reported that low plasma adropin levels are associated with obesity, obesity-associated insulin resistance, obesity-related non-alcoholic fatty liver disease, atherogenesis, diabetes, aging, child obstructive sleep apnea, and many other metabolic diseases, although some studies have come to inverse conclusions (Lovren et al., 2010 2010 ; Lian et al., 2011 2011 ; Butler et al., 2012 2012 ; Celik A. et al., 2013 2013 ; Celik E. et al., 2013 2013 ; Gozal et al., 2013 2013 ; Topuz et al., 2013 2013 ; Sayın et al., 2014 2014 ; Wu et al., 2014 2014 ; Zhang et al., 2014 2014 ). However, adropin has been confirmed as a potential, novel blood-based protein biomarker for several diseases (Lian et al., 2011 2011 ; Aydin et al., 2014 2014 ; Yildirim et al., 2014 2014 ; Yu et al., 2014 2014 ). It is significant that adropin also influences the regulation of food intake and body weight. Adropin controls the energy store, devoid of Enho- induced increased adiposity and insulin resistance in mice (Ganesh-Kumar et al., 2008 2008 ; 2012 2012 ). It also controls energy expenditure by regulating physical activity and motor coordination via the NB-3/Notch signaling pathway (Wong et al., 2014 2014 ). Adropin regulates muscle substrate preference under different nutritional states and promotes carbohydrate oxidation over fat oxidation (Gao et al., 2014 2014 ). Meat is the main source of protein in the human diet and pork accounts for more than one third of meat consumption (Zhang et al., 2012 2012 ; Henchion et al., 2014 2014 ). Thus, research into adropin and the energy balance of pigs has practical significance for the quality and quantity of pork production (Qiu et al., 2014 2014 ). Though the human, mouse, and bovine Enho genes have been cloned, the sequence of the porcine Enho was still unknown. In the present study, the porcine Enho ( pEnho ) was cloned and its expression profile determined. The results will promote energy balance regulation by adjusting diets via pEnho (Ganesh-Kumar et al., 2008 2008 ; St-Onge et al., 2014 2014 ). Pigs are considered to be a suitable animal model for studying human nutrition due to their apparent similarities with humans (van der Laan et al., 2010 2010 ; He et al., 2012 2012 ), and the cloning of the pEnho will also benefit the study of human metabolic diseases. Materials and methods 1 Animal raising and tissue sample collection 2 Twenty-four healthy piglets from six litters were purchased from Hunan Ground Biological Science and Technology Co., Ltd. (Changsha, China), and raised in the Laboratory Animal Center of the Institute of Subtropical Agriculture, Chinese Academy of Sciences (Changsha, China). All piglets were freely nursed by sows. At 1, 7, 14, and 21 d of age, all piglets were executed by jugular puncture under general anaesthesia via intravenous injection of 4% sodium pentobarbital solution (40 mg/kg body weight), and then immediately eviscerated (Yao et al., 2008 2008 ). The small intestines were separated and cleaned several times with ice-cold phosphate-buffered saline. Samples of liver, muscle, anterior jejunum, posterior jejunum, and ileum were collected and immediately frozen in liquid nitrogen, and stored at −70 °C until analysis. All procedures were approved by the Animal Care Committee at the Chinese Academy of Sciences (No. ISA2010007). RNA extraction and complementary DNA (cDNA) synthesis 2 Total RNA was extracted from samples using TRIzol® Reagent (Invitrogen-Life Technologies, CA, USA) following the manufacturer’s suggested protocol and dissolved in diethyl pyrocarbonate (DEPC)-treated water. The quality and concentration of extracted RNA were checked by 1.2% (0.012 g/ml) agarose gel electrophoresis and spectrophotometry using NanoDrop® ND2000 (NanoDrop Technologies Inc., DE, USA), respectively. Then, 1.0 μg of total sample RNA was incubated with DNase I (MBI Fermentas GMBH, St. Leon-Rot, Germany) and reverse-transcribed with mix primers using the Reverse Transcription System (Promega Co., WI, USA). Finally, the cDNAs were stored at −70 °C before further processing (Tan et al., 2011 2011 ). Cloning of the pEnho 2 Primers to recognize the pEnho cDNA sequence were designed with Primer 5.0 (Premier Biosoft International, CA, USA) based on the conserved nucleotide acid sequence of mouse and human Enho genes. The full-length cDNA of pEnho was amplified using the mixed cDNA from all tissues as a template. The primers used for cloning were 5'-CGGGCTCAACTCAGGCTCAG-3' as forward primer and 5'-CCCTCTCATTATTGCCGTGGA-3' as reverse primer. The polymerase chain reaction (PCR) mixture (25 μl total volume) contained 12.5 μl of 2× Taq PCR master mix (Tiangen, Beijing, China), 8.5 μl of ddH 2 O, 2 μl of mixed cDNA, and l μl (10 nmol/L) of each primer. The PCR reaction was performed using Eppendorf Mastercycler (Eppendorf, Hamburg, Germany) with the following parameters: initial denaturation at 94 °C for 5 min; 35 cycles of denaturation at 94 °C for 60 s, annealing at 55 °C for 60 s, and elongation at 72 °C for 60 s; and final elongation at 72 °C for 10 min. PCR products (4 μl) were identified by electrophoresis at 12 V/cm for 50 min on a 1% (0.01 g/ml) agarose gel. The amplification products were extracted from the gel using Promega Wizard SV Gel and the PCR Clean-up System (Promega Corporation, WI, USA). Then, the purified PCR products were cloned into the PMD™18-T Vector (TaKaRa, Dalian, China) and sequenced at Invitrogen (Guangzhou, China) (Wang et al., 2009 2009 ; Geng et al., 2011 2011 ). Real-time quantitative reverse transcriptase-PCR (RT-PCR) expression analysis 2 The expression profile of pEnho was determined by real-time RT-PCR analysis. Primers were designed with Primer 5.0 (Premier Biosoft International, CA, USA) based on the pEnho cDNA sequence. The primers used for RT-PCR of pEnho were 5'-GCTGCTCTGGGTCATTCTCTG-3' as forward primer and 5'-CTTCATGGCTGGGCTTCTG-3' as reverse primer. GAPDH was used as a reference gene, and primers were 5'-GAAGGTCGGAGTGAACGGAT-3' as forward primer and 5'-CATGGGTAGAATCATACTGGAACA-3' as reverse primer. RT-PCR was performed on the ABI PRISM 7900HT (Life Technologies, Carlsbad, CA, USA) platform using SYBR® Premix Ex Taq™ II (TaKaRa, Dalian, China) following the suggested protocol. The results were analyzed by ABI 7900 SDS software (Version 2.3, Applied Biosystems). Bioinformatics analysis 2 The BLAST program was used to identify homologous sequences in the GenBank database. Sequences were aligned with the multiple alignment program Clustal W 1.83 ( http://www.clustal.org http://www.clustal.org ). The neighbor-joining method was used to construct a phylogenetic tree using the PHYLIP software package ( http://evolution.genetics.washington.edu/phylip http://evolution.genetics.washington.edu/phylip ). Prediction of transmembrane helices in AA sequence was analyzed by TMHMM Server v. 2.0 ( http://www.cbs.dtu.dk/services/TMHMM/ http://www.cbs.dtu.dk/services/TMHMM/ ). The most likely signal peptide cleavage site of adropin was predicted using neural network (NN) models and hidden Markov models (HMM) from the SignalP 3.0 Server ( http://www.cbs.dtu.dk/services/SignalP http://www.cbs.dtu.dk/services/SignalP ). Potential cleavage site for mitochondrial pre-sequence was predicted using the Gavel program (Gavel and von Heijne, 1990 1990 ). Motifs were predicted using the Motif Scan program ( http://myhits.isb-sib.ch/cgi-bin/motif_scan http://myhits.isb-sib.ch/cgi-bin/motif_scan ). Adropin’s sub-cellular localization was predicted using program NNCN discrimination and the k -NN Prediction program ( k =23) ( http://psort.hgc.jp http://psort.hgc.jp ). Protein secondary structure prediction was carried out using the Garnier program ( https://npsa-prabi.ibcp.fr/cgi-bin/npsa_automat.plpage=npsa_gor4.html https://npsa-prabi.ibcp.fr/cgi-bin/npsa_automat.plpage=npsa_gor4.html ). Helix-turn-helix, zinc finger, leucine zipper and helix-loop-helix motifs in porcine adropin were predicted using Helixturnhelix program (Helixturnhelix program). Statistical analysis 2 To determine the changes in pEnho mRNA expression, multiple comparisons of mRNA abundance among anterior jejunum, posterior jejunum, ileum, liver, and dorsal muscle at Days 1, 7, 14, and 21 were carried out using the Duncan test after analysis of variance (ANOVA) using SPSS 20.0 (SPSS Inc., Chicago, IL, USA). Data are presented as mean±standard error of the mean (SEM). Significance was determined at P < 0.05 level. Results 1 Identification and characterization of pEnho cDNA 2 Using PCR, a fragment of approximately 763 base pair (bp) was sequenced. The sequence analysis revealed that the fragment was homologous to none of the known porcine genes. It was then submitted to the GenBank datebase (GenBank accession No. GQ414763). The open reading frame (ORF) of pEnho cDNA of 231 bp encoded a 76-amino acid (AA) polypeptide (Fig. 1 1 ). Hydrophobicity analysis of the AA sequence showed there was one putative trans-membrane helix between the 10th and the 32nd AAs (if the AA number of the helix is larger than 18, it is very likely to be a trans-membrane protein or have a signal peptide). The 1st to the 9th AAs lie outside the cell membrane and the 33rd to 76th lie inside the cell membrane (Fig. 1 1 ). Signal peptide analysis of the AA sequence showed that the most likely cleavage site was between positions 33 and 34 using NN models, and between positions 38 and 39 using HMM from the SignalP 3.0 Server (Fig. 1 1 ). Using the Gavel program, there is a potential cleavage site for mitochondrial presequence at SRS-AN (Fig. 1 1 ). Using the Motif Scan program, there are an N -myristoylation patter (MGAAISQ), a casein kinase II phosphorylation site (positions 43–46, SLSE), and a tyrosine kinase phosphorylation site (positions 65–72, KPSHEQSY) (Fig. 1 1 ). Program NNCN discrimination and the k -NN Prediction program ( k =23) were used to predict adropin’s sub-cellular localization. The results indicated that adropin can enter the nucleus with 94.1% and 100% probability, respectively. Phylogenetic analyses of the gene and AA sequence were performed, and the resulting neighbor-joining tree showed that the pEnho had a closer relationship to the bovine than the human and mouse genes (Fig. 2 2 ). Analysis of gene homology indicated that the pEnho was 98% similar to the bovine gene, 94% similar to the human gene, and 93% similar to the mouse gene (Fig. 3 3 ). Analysis of protein homology indicated that there was only one AA difference between bovine and pig adropin. Human and mouse adropin share the same AA sequence (Fig. 4 4 ). Protein secondary structure prediction was carried out using the Garnier program. The result indicated that human, pig, bovine, and mouse adropin share similar protein secondary structure (Fig. 5 5 ). The numbers on the right refer to the positions of the nucleotides. The stop codon is indicated by “*”. In the amino acid sequence, the potential N -myristoylation site (light gray boxed area), tyrosine kinase phosphorylation site (empty boxed area), casein kinase II phosphorylation site (ellipse area) and potential cleavage site for mitochondrial preseq (black boxed area) are indicated. A signal peptide sequence or a trans-membrane domain is indicated by “_” The unrooted tree was constructed using the neighbor-joining (NJ) method based on the alignment of the complete AA sequences (a) and gene sequences (b) of known vertebrate Ehno genes. Bootstrap values (1000 replicates) indicating the occurrence of nodes are reported above each branch in the figure Multiple sequence alignment was generated using Clustal W 1.83 Multiple sequence alignment was generated using Clustal W 1.83. The resulting alignment file was analyzed with Version 3.21 of BOXSHADE Protein secondary structure prediction was made using the Garnier program Relative abundance of pEnho mRNA at different ages and in different tissues 2 The tissue distribution of pEnho is shown in Table 1 1 . pEnho transcript expression was detected in all tissues including liver, muscle, jejunum, and ileum. To investigate the expression profile of pEnho in the porcine small intestine, the pEnho mRNA levels in three segments were compared by quantitative RT-PCR. The ileum has the highest pEnho expression. The developmental change in the relative abundance of pEnho mRNA is shown in Table 1 1 . The amount of pEnho mRNA in all tissues was highest at Day 7. The abundance of pEnho mRNA at Days 1 and 7 was greater than that at Days 14 and 21 (Fig. 6 6 ). All results were normalized using GAPDH mRNA as an internal control in each real-time PCR. The relative abundances of pEnho transcript expression in liver, muscle, proximate jejunum, distal jejunum, and ileum were analyzed by the 2 −ΔΔ C T method. Values are expressed as mean and SEM ( n =6). Values not sharing common superscript letters are significantly different at P < 0.05 2 Tissue 4 Relative abundance 2 SEM 2 P -value Day 1 Day 7 Day 14 Day 21 Liver 1.057 b 3.863 a 0.400 c 0.243 c 0.187 0.001 Muscle 1.143 bc 2.487 a 1.560 ab 0.313 c 0.517 0.018 Proximate jejunum 2.410 a 2.947 a 0.373 b 0.437 b 0.541 0.002 Distal jejunum 3.080 a 2.420 a 0.517 b 0.367 b 0.559 0.003 Ileum 5.337 b 7.967 a 0.347 c 0.367 c 0.516 0.001 All samples were normalized using GAPDH . Data are expressed as mean±SEM ( n =6). * P < 0.05, * * P < 0.01, *** P < 0.001 Discussion 1 We cloned the pEnho gene and found it similar in size (231 bp) to Enho genes reported in other animals (Fig. 3 3 ). Porcine adropin cloned by the pEnho shows high overall identity (98%–99%) with other known adropins (Fig. 4 4 ) and clusters with bovine adropin in the reconstructed phylogenetic tree for either the gene or protein (Fig. 2 2 ). TMHMM 2.0 program analysis revealed a putative trans-membrane or signal peptide in porcine adropin. However, using the NNCN program (Reinhardt’s method for Cytoplasmic/Nuclear discrimination) and the k -NN Prediction program, we found the porcine adropin predictive sub-cellular localization site in the nucleus with 94.1% and 100% reliability, respectively. So, we infer the existence of a nuclear, rather than trans-membrane, localization signal in porcine adropin. After processing and modification, porcine adropin enters the nucleus with the signal peptide, the signal peptide is then cleaved at SRS-AN and the residue of porcine adropin enters the nucleus where it functions. We then used the Helixturnhelix program to predict if helix-turn-helix motifs exist in porcine adropin. The result indicated that there were no helix-turn-helix motifs, nor zinc finger, leucine zipper nor helix-loop-helix motifs in porcine adropin (Fig. 5 5 ). This means that porcine adropin may not be a transcription factor (regulating the relative genes’ expression after directly combining with the nucleus). Using the Motif Scan program, we found the presence of N -myristoylation patter MGAAISQ, a casein kinase II phosphorylation site (positions 43–46, SLSE) and a tyrosine kinase phosphorylation site (positions 65–72). Thus, porcine adropin could be a secreted protein with a nuclear localization signal, which could regulate the expression of some genes as an adaptor molecule in some signal paths. Our results indicated that the abundance of pEnho mRNA was higher in 7-d-old piglets than in 1-d-old piglets in the liver, muscle, and ileum (Table 1 1 ). Ganesh-Kumar et al. ( 2008 2008 ) found that pEnho transcription in the liver was reduced with fasting and stimulated by food intake. The increase of pEnho transcription in piglets after birth may be associated with milk intake. Qiu et al. ( 2014 2014 ) found that adropin concentration was significantly correlated with gestational age at birth and cord blood adropin levels were positively correlated with gestational age. We speculate that age may be another factor for the increase of pEnho mRNA from Day 1 to Day 7 after birth in the tissues of piglets. Milk fat is significantly important for animals in the suckling period, especially in the early newborn period (Neel, 1962 1962 ), as it provides most of the energy for young animals. Milk, especially colostrum, contains a lot of fat. Many studies have shown that the transcription of pEnho mRNA increases with fat intake (Ganesh-Kumar et al., 2008 2008 ; Aydin et al., 2013b 2013b ). The fat in colostrum may increase the expression of adropin in piglets after birth. Also, we observed that the abundance of pEnho mRNA decreased rapidly from Day 7 after birth in all tissues (Table 1 1 ). The content of fat in colostrum is higher than in milk, and the percentage of fat in milk gradually decreases during the suckling period (Oosterveer et al., 2009 2009 ; Aydin et al., 2013b 2013b ). The reducing milk fat content may be responsible for the significant decrease in the abundance of pEnho mRNA in tissues from Days 7 to 21 after birth. At the same time, adropin levels in the colostrum of healthy mothers were shown to be higher than those in the mature milk (Aydin et al., 2013b 2013b ), and adropin levels correlate negatively with age ( r =−0.263, P =0.003) (Butler et al., 2012 2012 ). These factors also play important roles in pEnho mRNA abundance and adropin expression. The tissue distribution of Enho has been examined previously in several adult mammals, but few studies have investigated the distribution of Enho in developing animals, especially during lactation. The tissue distribution of Enho has been examined previously for humans, where Enho mRNA is more abundantly expressed in the liver than in the kidney and brain (Ganesh-Kumar et al., 2008 2008 ). Surprisingly there are no data about the expression of Enho in intestine. Adropin is synthesized in many tissues, including renal, heart, pancreas (Kuloglu and Aydin, 2014 2014 ), and liver tissue (Aydin et al., 2013b 2013b ) as well as milk, cheese whey, plasma (Aydin, 2013 2013 ), umbilical vein (Lovren et al., 2010 2010 ), and salivary glands (Butler et al., 2012 2012 ), but it is primarily synthesized and secreted from the liver where it changes the expression of lipogenesis genes (Ganesh-Kumar et al., 2008 2008 ). However, our data indicate that pEnho mRNA was higher in the intestine than in the liver for 1-d-old and 7-d-old piglets (Fig. 6 6 ). The mRNA can enter colostrum by exocytosis (Izumi et al., 2012 2012 ), the reason may be that colostrum contains pEnho mRNA at a higher level than in the liver of newborn piglets. Some researches have indicated that normal adropin concentration in human blood varies between (3.1±1.3) ng/ml (Celik E. et al., 2013 2013 ), 3.4–4.5 ng/ml (Butler et al., 2012 2012 ), and around 10 ng/ml (Aydin et al., 2013b 2013b ), and in human milk varies from approximately 9 to 14.5 ng/ml (Aydin et al., 2013b 2013b ). That means there is more adropin in milk than in blood. Adropin in blood mainly comes from the liver. We infer that the adropin content of milk is more than the amount of hepatic adropin synthesis. Further, pEnho mRNA abundance in milk is much higher than that in liver. The intestine absorbs the pEnho mRNA from colostrum, so, the level of pEnho mRNA is higher in the intestine than in the liver. The adropin content of the milk may be so high because it performs important functions, for example, promoting proliferation, migration, and capillary-like tube formation of endothelial cells (Lovren et al., 2010 2010 ), regulating the postnatal growth and development of different organs in the newborn (Qiu et al., 2014 2014 ), or reducing metabolic and oxidative stress in the lactating sow (Ganesh-Kumar et al., 2008 2008 ; 2012 2012 ; Celik E. et al., 2013 2013 ). The pEnho mRNA level in the liver, muscle, and ileum is higher for 7-d-old than 1-d-old piglets perhaps because the liver enhances the expression of pEnho mRNA during the first 7 d of a piglet’s life. Our results from PCR and quantitative RT-PCR analyses revealed that in 1-d-old piglets Enho abundance was low in the liver and muscle and high in small intestine; in 7-d-old piglets Enho abundance was low in the muscle and jejunum and high in the liver and ileum (Fig. 6 6 ). There were no significant differences of pEnho expression among all tissues in 14-d-old and 21-d-old piglets (Fig. 6 6 ). Developmental changes in intestinal function occur in the perinatal period of many species. For pigs and other mammals, the period between birth and weaning is characterized by rapid growth of the intestine, with energy utilization rate exceeding that measured at other stages of development. After birth, the developing piglet small intestine faces major changes in the functional demands that are placed on it. Adropin could influence the regulation of metabolic pathways and the postnatal growth and development of different organs in the newborn. 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All institutional and national guidelines for the care and use of laboratory animals were followed. 10.1631/jzus.B1400260 Project supported by the National Natural Science Foundation of China (No. 31302003), the Key Program of Hunan Province Scientific and Technology Planning Project (No. 2100CK2006), the Special Fund for Innovative and Entrepreneurship Talents of Changsha City (No. K1307006-21), and the Key Program of Changsha Scientific and Technology Planning Project (No. K1201108-21), China 2014-09-26 2015-05-13 2015-03-12 2022-01-05 Copyright © Zhejiang University and Springer-Verlag Berlin Heidelberg 2015 2015 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 06 16