Molecular Cloning and Function Characterization in Feeding of Neuropeptide Y in Gibel Carp, Carassius auratus gibelio.
Keywords: Gibel carp, neuropeptide Y, Cloning, Fasting, Feeding.
Feeding is a complicated behavior involving food ingestion and appetitive behavior, which reflects the motivation for food intake (Keen-Rhinehart et al., 2013; Simpson and Balsam, 2016). Furthermore, it is an important process in mammals (Valassi et al., 2008) and fish (Volkoff, 2016). Feeding is ultimately regulated by receiving and transducing endocrine signals from the central nervous system and periphery tissues (Begg and Woods, 2013; Keen-Rhinehart et al., 2013; Volkoff, 2016; Woods and Begg, 2016). To date, many appetite-regulating peptides have been identified in fish including cocaine, leptin (Zhang et al., 1994), ghrelin (GRLN) (Zhou et al., 2016), peptide YY (PYY) (Holzer et al., 2012), neuropeptide Y (NPY) (Wei et al., 2014; Volkoff, 2016).
Although lots of research on food intake in fish has progressed in the last few years, very little attention has been paid to the endocrine regulation mechanism of food intake. How to strengthen the production performance of fish through appetite regulation is still a hot research area.
Since neuropeptide Y (NPY) was first extracted from a mammalian brain in 1982 (Tatemoto et al., 1982), many studies have found that the npy mRNA is expressed in the central nervous system, peripheral nervous system and peripheral tissues of mammals and teleosts, with the highest expression in the brain (Chen and Li, 2005; Kehoe and Volkoff, 2007; Malmstrom, 2001; Murashita et al., 2009). NPY is a highly conserved neuroendocrine peptide (Hoyle, 1999), which is involved in the regulation of multiple physiological functions, such as circadian rhythms (Thorsell and Mathe, 2017), body temperature (Bouali et al., 1995), food intake (Wei et al., 2014), blood pressure (Dahlof et al., 1985) and sexual behavior (Clark et al., 1985; Inaba et al., 2016). In general, it is a multifunctional complicated hormone that governs various physiological processes in several animals.
In recent years, several researchers have reported that NPY and its related peptides are important in feeding in mammals and fish (Xu et al., 2015; Zhang et al., 2017). In Schizothorax prenanti, the npy expression level in fed fish was lower than in fasting fish (Wei et al., 2014). A similar result was found in other fish, such as Cyprinus carpio (Tang et al., 2014), Danio rerio (Dalmolin et al., 2015) and Seriola quinqueradiata (Hosomi et al., 2014), suggesting that NPY plays an orexigenic role in teleost fish. However, the npy expression level was elevated after feeding in Atlantic salmon (Valen et al., 2011). Differences in these studies could be due to sh species, age, size, and also to the physiological differences among different sh species (Chen et al., 2016; Fuentes et al., 2012; Volkoff et al., 2017). Therefore, further study is needed to validate the molecular mechanisms and biological function of NPY in feeding in fish.
Gibel carp (Carassius auratus gibelio), one of the major farmed fish species in China, has been subjected to major breeding efforts with high yield. So far, in gibel carp, most studies on the appetite and feeding modes have emphasized the effectiveness of the diet (Yin et al., 2017), but only little attention was given to the molecular regulation mechanism of food intake. Research on the biological function of NPY in feeding in gibel carp has not been described.
Here, we identified the gibel carp npy mRNA sequence and analyzed its expression patterns in different tissues. Furthermore, we analyzed the change in npy mRNA expression level between postprandial and fasting status using real-time quantitative PCR (RT-qPCR). This study provides the foundation for further investigation into the molecular mechanisms regulating food intake in gibel carp.
Materials and methods
Based on the Regulations for the Administration of Affairs Concerning Experimental Animals (Ministry of Science and Technology, China, revised in June 2004), all the research that involved animals was approved by the Institutional Animal Care and Use Committee in the College of Animal Science, Southwest University, Chongqing, China. The feeding conditions, including dissolved oxygen and temperature were under strict control.
All the gibel carp were purchased from a local nursery of fish in Chongqing, China, and then transported to the laboratory in the Aquaculture Department at Southwest University. Before the experiments, the fish were in a circulating aquarium system at 23 +- 2AdegC for 14 days and fed a commercial diet (6% fat and 40% crude protein, Haida, Guangzhou, China) once a day (17:00).
According to an overview about regulation of food intake in fish (Volkoff, 2016), npy is highly expressed in the brain. Therefore, for the cloning study, brain samples were collected from six fish with a mean body weight of 293.5 +- 17.56 g(1:1 gender ratio). For the tissue distribution study, 21 tissues were collected from six fish with a mean body weight of 316.33 +- 11.7 g (1:1 gender ratio; for more information about the 21 tissues see section 2.3).
To conduct the postprandial research, seven groups of weight-matched fish with a mean body weight of 308.7.36 +- 17.5 g (n = 15/group) were allowed to acclimate to the tank conditions (110 x 44 x 44 cm3). In terms of the feeding activity and behavior, no difference was observed between the tanks. The fish were sampled before the feeding (-3 h and -1 h), at commencement of feeding (0 h) and after feeding (+1 h and +3 h). For the unfed control groups, two unfed groups were sampled at +1 and +3 h. Six individuals were sampled for every sampling point and group.
For the long fasting study, fish with a mean body weight of 458.33 +- 20.1 g (n = 30 x 6, three tanks of unfed fish and three tanks of fed fish) were sampled. After 2 weeks of feeding, three groups' fish were endured fasting, while other three groups' fish were fed as before. The fasted group's fish were sampled severally on day 1, 3, 5 and 7. Six fish in the fed group were sampled at every sampling point. The fasted group was fed again on day 9 on a regular basis, and six fish were sampled on day 9, 11 and 14.
Tissue collection and RNA extraction
Before being sacrificed, fish were anesthetized with tricaine methanesulfonate (MS-222, 0.02%). Then, 21 tissues (telencephalon, hypothalamus, mesencephalon, cerebellum, myelencephalon, liver, spleen, heart, eye, skin, foregut, gill, white muscle, hindgut, midgut, red muscle, trunk kidney and gonad) were removed immediately and stored in liquid nitrogen. RNA was extracted from these tissues with TRIzol A+ reagent, according to the manufacturer's instructions (TaKaRa, Dalian, China). The concentration of all the RNA samples was determined by a photometer (Thermo Scientific, Dreieich, Germany) at 280 nm and 260 nm. Until further use, the total RNA was stored at -80AdegC.
RNA (around 2 ug) was used for first strand synthesis of cDNA with a Prime Script RT reagent Kit (TaKaRa, Dalian, China). The primers for npy fragment amplification were designed based on npy sequences of other fish species found in the NCBI GenBank.
SMART RACE cDNA Construction Kit (Clontech, USA) was used to synthesize the entire brain's first-strand cDNA with 3' or 5' adaptors for cDNA ends (RACE) PCR rapid amplification. 3' and 5' RACE PCR were conducted to obtain the sequence of the full-length gibel carp npy. The RACE PCR products were obtained from the nested RACE PCR for npy's 3' and 5' RACE. Based on the npy fragment, the primers for the gibel carp npy gene were designed. The PCR conditions were: 5 cycles of 94AdegC for 30 s and 72AdegC for 180 s; 5 cycles of 94AdegC for 30 s, 70AdegC for 30 s and 72AdegC for 180 s; 20 cycles of 94AdegC for 30 s, 68AdegC for 30 s and 72AdegC for 180 s. The PCR product was separated by agarose gel electrophoresis (1.5%). Next, the target bands were extracted by a Universal DNA Purification Kit (TIANGEN, Beijing, China). Subsequently, the PCR fragments were ligated to a pMDA(r)19-T plasmid (TaKaRa, Dalian, China).
The ligated plasmid was transformed into Escherichia coli DH5[alpha]. Colonies with inserts were cultured in LB medium at 37AdegC overnight. OMEGA Mini Plasmid Kit (TaKaRa, Dalian, China) was used to extract the plasmids from the colonies, which were then sequenced by an automated sequencing study.
Multiple sequence alignments were generated using the clustalx1.83. The cleavage site of the signal peptide was estimated using the SignalP Ver. 4.0 program (http://www.cbs.dtu.dk/services/SignalP/). A phylogenetic tree based on the amino acid sequences was constructed by the neighbor-joining method of the Clustal W (http://www.ddbj.nig.ac.jp/search/clustalw-e.html) (Thompson et al., 1994) and MEGA 5.1 programs (http://www.megasoftware.net/index.html) (Kumar et al., 2004).
Real-time quantitative PCR
Real-time quantitative PCR (qPCR) was used to evaluate the tissue distribution, postprandial variations and fasting effect on npy mRNA. According to the sequence information gained from cloning (Table I), gene-specific primers were designed for qPCR. SYBR Green (TaKaRa) was used to conduct the qPCR on npy with QuantStudio(tm) 3 Real-Time PCR (ABI) (TaKaRa). All the real-time qPCR reactions were carried out in triplicate. Every PCR reaction (total volume, 25 uL) included 9.5 uL of RNase-free H2O, 2.5 uL of cDNA, 0.5 uL of each primer and 12.5 uL of 2xSYBR Premix Ex TaqTM. To analyze the samples, the 2-IICt method was used to determine the mRNA abundance. The amplification reaction conditions were: 95AdegC for 30 s, followed by 45 cycles of 95AdegC for 5 s and 60AdegC for 30 s. In this research, 18S and [beta]-actin were used as housekeeping control genes.
The normality test was performed before the Student's t-test or one-way analysis of variance with SPSS 18.0 software (SPSS Inc., Chicago, IL, USA), to ensure that the t-test is suitable for data comparison. Data were expressed as means +- SEM. P < 0.05 was considered statistically significant.
Table I.- Primers used for sequences.
Primer name###Sequence (53)###Application
NPY3-F1###TGTCAGCACTGGACCTTTTGCCATACCT###NPY 3RACE outer
NPY3-F2###ACCCTTCCGTTAGAGTTCCCAAGCAGAC###NPY 3RACE inner
NPY5-F1###CTGCTTGGGAACTCTAACGGAAGGGTAT###NPY 5RACE outer
NPY5-F2###ATAACACGGCAGAGGTATGGCAAAAGGT###NPY 5RACE inner
NPY-F###CCTTCCTCTTGTTCGTCTGCT###Real time PCR
NPY-R###TGCCATACCTCTGCCGTGT###Real time PCR
[beta]-Actin-F###CGAGCTGTCTTCCCATCCA###Real time PCR
[beta]-Actin-R###TCACCAACGTAGCTGTCTTTCTG###Real time PCR
18s F###ACCACCCACAGAATCGAGAAA###Real time PCR
18s R###GCCTGCGGCTTAATTTGACT###Real time PCR
Sequence analysis of the gibel carp npy gene
The complete Open Reading Frame (ORF) of the gibel carp npy mRNA is 291 bp, encoding 96 amino acids including a 28-amino-acid signal peptide and a 36-amino-acid mature peptide (Fig. 1; GenBank accession No. MF805788).
Gibel carp NPY has a lower similarity to mammalian NPY (74% with Mus musculus) than to cyprinid NPY (98% with Carassius auratus and 99% with Schizothorax prenanti; Fig. 2). The phylogenetic analysis revealed that the gibel carp NPY was grouped with the Cyprinid fish cluster (Fig. 3).
Tissue distribution of npy in gibel carp
We investigated the expression level of npy mRNA in 21 tissues of gibel carp. As shown in Figure 4, the highest expression was found in the hypothalamus, eye and myelencephalon. The lowest expression of npy mRNA was observed in the liver, heart, gill, pituitary and hindgut.
The effect of food on npy mRNA expression in gibel carp
As shown in Figure 5, after 1 and 3 h of feeding, the npy mRNA expression in the hypothalamus was significantly lower in the fed group compared with the unfed group (P < 0.01). The npy mRNA expression of unfed group at +1h and +3h was significantly higher than the npy mRNA expression at -3h,-1h and 0h (P < 0.05).
The effect of long fasting on npy mRNA expression in gibel carp
As shown in Figure 6, on day 7, a significant change was detected between the fed group and the fasting group (P < 0.01). After refeeding, the expression of npy in the refed groups at 9, 11 and 14 days was significantly lower than that in the fed groups (P 0.05; Fig. 6).
In our research, we isolated from gibel carp a 291-bp ORF of npy, encoding 96 amino acids. Using multiple sequences alignment and phylogeny evolution analysis, we found that the sequence of this gene is highly homologous with other species, especially cyprinid fish. The results indicated that the gibel carp npy gene is highly conserved within teleost species.
To explore the gene's expression profile in gibel carp, npy mRNA was investigated in peripheral and central tissues by qPCR. The results showed that npy mRNA was highly expressed in the brain, especially in the hypothalamus, which is consistent with reports on other fish species, such as S. prenanti (Wei et al., 2014) and Atlantic salmon (Murashita et al., 2009). The hypothalamic neuronal circuitry is critical for the regulation of feeding behavior in vertebrates (Berthoud, 2002; Carr et al., 2002; Nuria and Thrur, 2001; Saper et al., 2002; Volkoff et al., 2005). Thus, it can be inferred from the results that npy may play a role in feeding regulation. Interestingly, we also found a high expression level in the eye. Similar result was also reported in the Sparus aurata L. (Pirone et al., 2008). We speculated that npy may be involved in modulating neurotransmitter release.
However, research on npy function in the eye is still inadequate and remains to be explored. In addition, npy was detected in the heart, foregut, ovary and testis. These results indicate that npy may be involved in a wide range of biological functions in gibel carp such as cardiac function (Xiang, 1994), gastrointestinal processes (Kehoe and Volkoff, 2007; MacDonald and Volkoff, 2009; Montpetit et al., 2005) and sexual behavior (Gaikwad et al., 2005; Peng et al., 1994).
Previous studies have demonstrated that npy is an important appetite-regulating hormone in mammals (Clark et al., 1984) and fish (Wei et al., 2014). The obtained data of the current study showed that 1 and 3 h after feeding, the npy mRNA expression in the hypothalamus was significantly lower in the fed group compared with the unfed group (P < 0.01). This result is consistent with previous studies on other fish. In goldfish, the brain npy mRNA levels sharply decreased at +1h and +3h after feeding (Narnaware et al., 2000). In S. prenanti, the expression level of npy in fed fish was significantly lower than that in unfed fish at 0.5, 1.5, 3 and 9 h after feeding (Wei et al., 2014). The npy mRNA expression of fasted fish at day 7 was significantly higher compared with the fed group (P < 0.01). On days 9, 11 and 14, the npy mRNA expression was significantly lower in the refed group than in the fed group (Fig. 6; P < 0.01).
These results are consistent with previous research on other species. In zebrafish, the npy mRNA expression in the hypothalamus was significantly increased after 7 days of fasting (Yokobori et al., 2012). In Chinook salmon and coho salmon, npy mRNA expression in the hypothalamus increased after fasting for 2-3 weeks (Silverstein et al., 1998). In Brazilian flounder, the npy mRNA expression in the brain after 2 weeks of fasting was higher than in fed fish (Campos et al., 2010). In summary, these results indicated that npy has an orexigenic role in gibel carp. Nevertheless, fasting did not affect the npy mRNA expression in Atlantic salmon (Murashita et al., 2009), suggesting that not all fish are alike in the endocrine regulation of feeding.
In our study, the npy gene was first identified from gibel carp. We found that it is highly expressed in the brain, especially in the hypothalamus. Furthermore, fasting caused its mRNA expression to change in gibel carp, suggesting that npy may have orexigenic activity in gibel carp. Our findings offer an essential foundation for future research on the regulating mechanisms and functions that underlie the role of npy in feeding in teleosts.
This study was supported by the Fundamental Research Funds for the Central Universities (No. XDJK2018C053) and the Youth Foundation of Southwest University Rongchang Campus (No. 132030/20700946) and the Ecological Fishery Industry Technology System of Chongqing (No. 134030/40800115).
Statement of conflict of interest
The authors declare no conflict of interest.
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|Author:||Lei, Luo; Deng, Xingxing; Yuan, Dengyue; Zheng, Zonglin; Zhu, Chengke; Luo, Hui; Li, Baohai; Ye, Hua|
|Publication:||Pakistan Journal of Zoology|
|Date:||Jun 30, 2019|
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