A Study on Differentially Expressed Genes in Reserve Mesenchyme of Male and Female Reindeer Antler Tip.
Reindeer is the only species in which the females carry antlers in Cervidae, and the differences between the antler tips of the two sexes are one of the most interesting scientific mysteries. The objective of this study was to isolate preliminarily differentially expressed genes in antler mesenchyme of both sexes. The genes were detected with three anchored primers and ten random primers using differential display reverse transcription PCR (DDRT-PCR). Five differentially expressed fragments were obtained through recovery, cloning and sequencing. Three of them (Af1, Ce1, Ci2) presented a higher expression in antler mesenchyme of female reindeer, but the other two (Ae1, Af3) were the opposite. The results of Blast in GenBank showed that they shared high homologies with SMAD5 (95%), COL6A3 (95%), SLC17A5 (93%), TPM4 (99%) and HMGB1 (98%), respectively.
Quantitative RT-PCR validation of gene COL6A3 showed that the expression in both sexes was consistent with the results of mRNA differential display, but there was no significant difference between the male and female.
Reindeer (Rangifer tarandus), Antler, Mesenchyme, mRNA differential display, RT-PCR.
Deer antlers are the only mammalian appendages capable of regeneration, represent one of the fastest rates of organogenesis in the animal kingdom, and provide a model for studying two unique processes: the development of a complete appendage that is delayed until puberty and mammalian organ regeneration. However, the reindeer (Rangifer tarandus) is the only species of deer in which both sexes normally produce antlers (Leader-Williams, 1979), and many gaps exist in morphology, growth period in antler of male and female reindeer. The early work mainly focused on the relationship with hormones and antler cycle of male and female reindeer to seek the differences between them. However, there is still a lack in understanding the interplay of differentially expressed genes involved in the antler growth of male and female reindeer. Here, we attempted to isolate and identify preliminarily the differentially expressed genes in antler mesenchyme between the both sexes of reindeer.
Given an outer fibrous perichondrium where type 1 collagen mRNA and protein are highly expressed and an inner, more cellular zone that cells are actively dividing (Price et al., 2005), the reserve mesenchyme, therefore, provides an ideal source for exploring the antler growth and may help in understanding the mechanism of the difference in antlers of male and female reindeer. Differential display reverse transcription PCR (DDRT-PCR), introduced firstly by Liang and Pardee (Liang and Pardee, 1992), can identify the total number of genes subject to up- or down-regulation in a particular setting and has been widely used to screen for genes that are differentially expressed (Breyne and Zabeau, 2001; Ahmed et al., 2000). Furthermore, Quantitative reverse transcription PCR was proved to eliminate the false positive rate to validate effectively the differential expression of genes.
To study its possible mechanism in response to the molecular machinery in the antlers between the male and female reindeer, we decided to perform a preliminary study to examine differences in the gene expression in relationship to antler mesenchyme of both sexes using the mRNA differential display method.
MATERIALS AND METHODS
Sample collection and preparation
The distal 5 cm from each antler was collected from two anaesthetized healthy reindeer at Grand Farm in Harbin, which were introduced from the Ewenki reindeer herding of Aoluguya, Inner Mongolia, China. The two reindeer are half-sib, the male is 6-year-old, and the female is 7-year-old. Following the established methods (Li et al., 2002), reserve mesenchyme was rapidly separated from five morphologically defined layers (dermis, reserve mesenchyme, precartilage, transition zone and cartilage; Fig. 1), and stored immediately in liquid nitrogen until further processing.
Extraction of RNA and synthesis of first-strand cDNA
Total RNA was isolated using Trizol reagent (Invitrogen) according to the manufacture's instructions. The RNA quality and integrity were examined with ultraviolet spectrophotometer and electrophoresed on 1.0% agarose gels. Three reverse transcription reactions were carried out for each RNA using three anchored primers. In each PCR tube, 4.0uL of total RNA (1ug/uL), 8.0uL 5x RTbuffer, 9.6uL dNTP (2.5mM), 0.5uL RNase inhibitor (10U/uL), 2.0uL anchored primer (10mM), 2.0uL M-MLV, (200U/uL, TOYOBO) were added, and ddH2O treated by diethypyrocarbonate (DEPC) was filled to the total volume of 40.0uL. The reverse transcription condition were 42degC for 20min, 99degC for 5min, and 4degC for 5min. The products of reverse transcription (cDNA) were detected with ultraviolet spectrophotometer, diluted to 1ug/uL and stored at -20degC for using as template for differential display PCR amplifications.
Each primer pair was composed of an anchored primer and a random primer (Table I, Invitrogen, Shanghai). PCR was carried out in a final reaction volume of 25uL containing 2.5uL 10 x buffer, 2.0uL MgCl2 (25mM), 2.0uL dNTP (2.5mM), 0.125uL rTaq DNA polymerase (5U/uL, TaRaKa, Japan), 4.0uL anchored primer (10mM), 0.8uL random primer (10mM), 2.0uL cDNA (1ug/uL), 11.575uL ddH2O. Amplifications were performed using the following PCR procedure: an initial denaturation step for 5 min at 94degC, followed by 40 cycles of 94degC for 30 s, 2min at 42degC and 1 min at 72degC, and a final elongation for 10 min at 72degC. PCR products were separated on 8% nondenaturing polyacrylamide gels.
Table I.- Anchored and random primer sequences for DDRT-PCR.
Recovery of differential fragments and their reamplifications
The differentially expressed bands were excised from the gel and washed two times. Then mashed the differentially expressed bands and added 25-35uL ddH2O to incubate at 100degC for 10 min. After that, the tubes were incubated for 5 min at room temperature and centrifuged at 5000 rpm for 5 min. We transferred DNA into a new PCR tube and stored at -20degC. The reamplification system was in 25uL volume being consistent with the differential display RT-PCR, except that the template was changed to the stored DNA. And PCR condition remained the same. The PCR products were electrophoresed on 1.0% agarose gels, then we carried out large scale amplification of the product with the same size to make the final product 80-100uL. The differentially expressed bands were excised from the gel and extracted by gel extraction kit (GALEN BIOPHARM).
Cloning and sequence analysis of differential fragments
The differential cDNA fragments were cloned into pMD 18-T vector (TaKaRa) according to the manufacture's instructions. The positive clones were sequenced by BGI (Beijing, China). The target sequences were obtained after the vector and primer sequences were kicked off. These target sequences were searched at http://blast.ncbi.nlm.nih.gov/Blast.cgi. The identity of the clones was determined from their similarity in the GenBank.
Quantitative RT-PCR verification of differential fragments
The reverse transcription condition was consistent with synthesis of first-strand cDNA, except that the anchored primer was Oligo dT (10mM). The cDNA was diluted ten times and stored at -20degC. The primer sequences of ss-actin (internal reference) and the differential fragments were designed with Primer Premiers 5.0 (Table II). The products of reverse transcription were used as the templates of another PCR reaction in a 25uL volume: 2uL template, 2.5uL 10 x PCR buffer, 2.5uL MgCl2 (25mM), 2uL dNTP (2.5mM), 0.125uL rTaq (5U/uL, TaKaRa), 2uL forward and reverse primers, and 15.375uL ddH2O. The PCR procedure was 94degC for 5 min, followed by 40 cycles of 94degC for 1 min, 1 min at 60degC and 72degC for 1.5 min, and a final elongation for 10 min at 72degC. The PCR products were inspected by electrophoresis on 1.0% agarose gels. PCR without template was performed as the negative control.
Table II.- Primer sequences used in RT-PCR.
Quantitative RT-PCR was performed with ABI 7500 and the reaction mixtures (10uL) consisted of 1uL cDNA, 5uL SYBR Premix Ex TaqTM (TaKaRa), 0.4uL forward and reversed primers, 3.6uL ddH2O. The PCR procedure was 95degC for 5 min, followed 40 cycles of 30s at 95degC, 1min at 60degC and 30s at 72degC, then dropped quickly to 60degC and heated up to 95degC slowly to establish the dissolution curve of products.
Final quantification was calculated by the comparative CT method (Martha et al., 2009). The CT for the target amplicon and the CT for the endogenous control were determined for each sample, and differences between them, called DCT, were calculated to normalize for the differences in the RNA extractions and the efficiency of the RT step. The difference between DCT for each experimental sample and DCT of the calibrator was called the DDCT value. Finally, the amount of target, normalized to the endogenous control and relative to the calibrator, was calculated by 2-DDCT. The differential genes were highly expressed as long as 2-DDCT[greater than or equal to]2 (P0.05, Table IV and Fig. 6).
Table III.- Differentially expressed fragments and their Blast results.
Differential###Primer###Gene/sequence in GenBank###Homology
Ae1###A/e###TPM4###NM_001101162###Bos taurus tropomyosin 4###99
Af1###A/f###SMAD5###XM_012178532###Ovis aries SMAD family member 5###95
Af3###A/f###HMGB1###BT030587###Bos taurus high-mobility group box1###98
Ce1###C/e###COL6A3###XM_005971413###Pantholops hodgsonii collagen, type VI, alpha 3###95
Ci2###C/i###SLC17A5###XM_005902349###Bos mutus solute carrier family 17###93
###(acidic sugar transporter), member 5
Table IV.- Differential expression of COL6A3 gene in antler mesenchyme of male and female reindeer.
###CT of gene COL6A3###CT of gene -actin###CT###CT###RQ###RQmin###RQmax
In our preliminary study, five differential expressed genes were isolated from mesenchyme in antlers of male and female reindeer using mRNA DDRT-PCR method, and they showed strong homology with genes of other species. Most of the genes indicated their alleged role related to the antler growth. Gene Ae1, Af1, Af3 and Ce1 were detected to be associated with the proliferation of antler tip, cellular transport and ossification mechanism, but gene Ci2 provides instructions for producing a protein called sialin that is located mainly on the membranes of lysosomes, compartments in the cell that digest and recycle materials, and further research remains to done to find the relationship with the antler molecular machinery. However, as one of the leading high-throughput technologies screening for changes in gene expression, differential display PCR has a shortcoming that it's not quantitative but qualitative.
Therefore, quantitative real-time PCR should be performed to validate the changes in differential expression. Comparing the relative gene expression identified by high throughput assays and real-time could determine if the gene was truly differentially expressed. For this purpose, we used SYBR green detection and product melting curve analysis to validate the results from differential display PCR technologies. Furthermore, we chose SYBR green detection rather than TaqMan probes aiming to increase the flexibility to quickly validate numerous genes identified by the high-throughput screen.
Gene Af1, presented a higher expression in antler mesenchyme of female reindeer than the male reindeer, was found to share a high homology (95%) with the Ovis aries SMAD family member 5 (SMAD5) that related to transforming growth factor (TGF-ss). Bone morphogenetic protein (BMP), as a member of TGF-ss superfamily, was found to induce the osteogenic activity. Besides, of the nine SMAD protein that were found, SMAD5 and SMAD1 are involved in the signal transduction of BMP (Hild et al., 2000). Previous study has reported that the BMP7- induced inhibition of TGF-ss-dependent profibrogenic activities in mesangial cells requires SMAD5 (Wang and Hirschberg, 2004). Then Retting and Buer reported that SMAD5 is required for endochondral bone formation (Retting et al., 2009).
In our study, we found that gene Af1 had a higher expression in antler mesenchyme of the female reindeer, probably due to the difference in antler ossification degree between the male and female reindeer when we sampled, in other words, the antler of female reindeer began to ossify and gene Af1 was up-regulated expression. Further research remains to done to explain the phenomenon.
Gene Ae1 was observed a higher expression in antler mesenchyme of male reindeer, and shared a high homology (99%) of Bos taurus tropomyosin 4 (TPM4), which is one of the four identified tropomyosin (TPM1, TPM2, TPM3, TPM4) involved in the regulation of muscle contraction and cell membrane transport (Spinner et al., 2002). It's reported that TMs may be broadly categorized into high- and low-Mr species depending on their size, and suppression of high-Mr tropomyosin (TM) occurs in malignant cells, suggesting a role for these proteins in neoplastic transformation (Raval et al., 2003). Besides, regulating the expression of TM could hinder the process of malignant transformation in cells (Prasad et al., 1999). We detected a higher expression of gene Ae1 in antler mesenchyme of male reindeer, and there were two conjectures: the male maybe need a higher expression of gene Ae1 to regulate cell carcinogenesis, and the antler of male reindeer may grow faster than the female.
The differentially expressed gene Af3 shared a high homology (98%) with Bos Taurus high-mobility group box1 (HMGB1), which is an important structural protein mainly distributed in mammalian cell nucleus (Suda et al., 2010). HMGB1 acts as a DNA chaperone, chromosome guardian, autophagy sustainer, and protector from apoptotic cell death inside of the cell, on the other hand, it's the prototypic damage associated molecular pattern molecule outside the cell (Rui et al., 2014). Therefore, the antler mesenchyme of male reindeer showed a higher expression of gene Af3, this may be one reason that the antler of male reindeer is obviously bigger than the female.
Gene Ce1 shared a high homology (95%) with Pantholops hodgsonii collagen, type VI, alpha 3 (COL6A3), whose primary role is in assembling collagen VI microfibrils (Te-Cheng et al., 2013). Collagen VI is the key component of bone and muscle, which mainly has the function of maintaining the integrity of the organization and guiding the signal transduction in the specific cell. Mutation in collagen VI genes cause congentital muscular dystrophy types Bethlem and Ullrich as well as intermediate phenotypes characterized by muscle weakness and connective tissue abnormalities. Collagen families were highly expressed in the antler tips using RNA-sequencing (Yang et al., 2015). In our study, gene COL6A3 presented a higher expression in antler mesenchyme of female reindeer, but there was no significant difference. Therefore, further studies to evaluate the function of COL6A3 gene related with antler growth regulation.
This study was designed for the identification of differentially expressed genes of antler mesenchyme between the male and female reindeer. We observed successfully the five differentially expressed genes and screened several candidate genes with respect to the regulatory genes of antler mesenchyme in both sexes reindeer. However, additional evidence is required in future.
This study was financially supported by the Fundamental Research Funds for the Central Universities (2572016AA42), and the Project for Field Rescue and Captive Breeding of Endangered Species of the State Forestry Administration of China (2013).
Statement of conflict of interest
Authors have declared no conflict of interest.
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|Author:||Zhai, Jiancheng; Gao, Li; Xia, Yanling; Li, Heping|
|Publication:||Pakistan Journal of Zoology|
|Date:||Jun 30, 2017|
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