Effect of Prokaryotic Expressed Nucleoplasmin on the Efficiency of Somatic Cell Nuclear Transfer in Banna Mini-pig Inbred Line

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PJZ_49_1_297-303

Effect of Prokaryotic Expressed Nucleoplasmin on the Efficiency of Somatic Cell Nuclear Transfer in Banna Mini-pig Inbred Line

Wenmin Cheng1,2*, Weirong Pan1,2, Yubo Qing1, Yingchao Liu1, Xingqin Zha1,2, Yan Huang2, Jige Xin1,2, Hongjiang Wei1 and Yangzhi Zeng2

1College of Animal Science and Technology, Yunnan Agricultural University, Kunming, Yunnan 650201, China

2Key Laboratory of Banna Mini-pig Inbred Line, Yunnan Agricultural University, Kunming, Yunnan 650201, China.

Wenmin Cheng and Weirong Pan contributed equally to this work.

ABSTRACT

Nucleoplasmin (Npm) is the most abundant protein in the nucleus of oocytes which can promote in vitro nucleosome formation. In this study, to improve the efficiency of SCNT in Banna Mini-pig Inbred Line (BMI), we obtained the recombinant nucleoplasmin (Npm) by using a prokaryotic expression system and compared the difference on the developmental effects between exogenous Npm and its structural analog, polyglutamic acid (PGA). We chose the pMD18-T vector for Npm expression and transformed E. coli BL21 (DE3) cells to construct a prokaryotic expression system. The results showed that the recombinant Npm protein of 32 kDa could be obtained. Recombinant Npm or PGA was injected into porcine oocytes at different concentrations. The results showed that the blastocyst rates in injection 560 ng/μL Npm and 1000 ng/μL PGA groups were higher than those of other groups. Moreover, the blastocyst rate was highest in injection 560 ng/μL Npm group and was lowest in injection 100 ng/μL PGA group. These data suggested that addition of recombinant Npm obtained by prokaryotic expression or PGA could improve the development of SCNT embryos in the BMI.

Article Information

Received 01 August 2015

Revised 15 September 2016

Accepted 21 September 2016

Available online 07 January 2017

Authors’ Contributions

WC conceived and designed the experiments. WC, WP, YQ, YL, YH, JX performed the experiments. WMC analyzed the data. XQC, YZZ contributed somatic cell. WC and WP wrote the paper. HW helped in preparation of manuscript.

Key words

Banna Mini-pig Inbred Line, Prokaryotic expression, Nucleoplasmin, Polyglutamic acid, Embryo development.

* Corresponding author: cheng_8097@163.com

0030-9923/2017/0001-0313 $ 9.00/0

DOI: http://dx.doi.org/10.17582/journal.pjz/2017.49.1.313.320

INTRODUCTION

Somatic cell nuclear transfer (SCNT) is an assisted reproductive technology that can be used in the farm animal production industry, drug production, regenerative medicine and conservation of invaluable genetic resources (Vajta, 2007; Oback, 2008). In addition, SCNT can provide unique and interesting experimental systems for genomic research to learn how the somatic cell genome is reprogrammed into an equivalent state to that of the fertilized oocyte (Gurdon and Wilmut, 2011). Since the birth of Dolly the sheep in 1996 (Campbell et al., 1996), many cloned animals have been produced in the cow (Kato et al., 1998), mouse (Wakayama et al., 1998), goat (Baguishi et al., 1999), pig (Polejaeva et al., 2000), rabbit (Chesné et al., 2002), cat (Shin et al., 2002), rat (Zhou et al., 2003), horse (Galli et al., 2003), mule (Woods et al., 2003), dog (Lee et al., 2005), ferret (Li et al., 2006), buffalo (Shi et al., 2007) and the camel (Wani et al., 2010).

Banna Mini-pig Inbred Line (BMI) has been bred since the 1980s from full and half siblings. As a unique, highly inbred pig line, BMI can be used in various biomedical studies, including disease models, transgenesis, genomics, and xenotransplantation for medical research (Crabbe et al., 2005).Although the cloned piglets of BMI had been obtained (Wei et al., 2013), the efficiency of nuclear transfer was between 0–2.5%, i.e., 0-5 live births after transfer of 200 cloned embryos. As with most cloning efforts, developmental defects, including abnormalities in cloned fetuses and placentas, high rates of pregnancy loss and neonatal death have often been encountered (Jiang et al., 2007). Reprogramming which is initiated by the oocyte following nuclear transfer (NT), continues during development may often be inefficient (Latham, 2004, 2005). So improving the efficiency of reprogramming may lead to greater cloning success (Blelloch et al., 2006).

Nucleoplasmin (Npm), as a molecular chaperone, was found in the eggs of Xenopus laevis which facilitated sperm chromatin remodeling at fertilization (Leno et al., 1993). It can help load histones onto DNA during nucleosome assembly in vitro (Laskey et al., 1978). Previous studies showed that Npm could be located in bovine oocytes (Fair et al., 2001) and porcine embryos (Hyttel et al., 2000). In addition, it was suggested that Npm could improve development of nuclear transfer embryos by facilitating reprogramming of the somatic cell nucleus in bovine (Betthauser et al., 2006). The acidic polyanion, polyglutamic acid (PGA), can also mediate sperm decondensation and nucleosome assembly in vitro (Dean, 1983). However, Npm has not yet been tested to improve developmental competence of BMI nuclear transfer embryos. Moreover, whether PGA enhances the developmental ability of BMI nuclear transfer embryos is presently unknown.

The aim of this study was (i) to construct prokaryotic expression vector and obtain efficiently expressed Npm, and (ii) to examine the difference on the developmental effect between exogenous Npm and PGA.

MATERIALS AND METHODS

Materials

Escherichia coli strains DH5α, pCold II vector and LB medium were prepared at Invitrogen Shanghai Co. Ltd. (Shanghai, China). The pMD18-T vector was purchased from TaKaRa Biotechnology Co. Ltd. (Dalian, China). The BL21 (DE3) and pG-TF2 expression strain, platinum Taq DNA polymerase high fidelity, all restriction enzymes, DNA molecular mass markers and the PCR product purification kit used in this study were purchased from Life Technologies Corporation (Invitrogen, Carlsbad, California, USA). Chemicals and reagents used in oocyte and embryo culture, unless otherwise stated, were purchased from Sigma-Aldrich Co. (St. Louis, MO, USA).

Synthesis of the Npm2 gene

The full-length cDNA (GenBank accession No. NM_001195362.1) of Npm2 gene contains 660 nucleotides, which encodes a protein of 219 amino acid residues. Oligos of Npm2 gene were synthesized and assembled by PCR, containing Nde I and Hind III restriction sites. The reaction was carried out using the following reaction cycles: initial denaturation at 94°C for 5 min followed by 28 consecutive cycles of denaturation at 94°C for 20 sec, annealing for 30 sec at 55°C, extension at 72°C for 1 min, then final extension at 72°C for 10 min. The amplified Npm2 gene was gel-purified by highly pure PCR product purification kit. The purified product was inserted into the corresponding region of pMD18-T expression vector according to operation manual, transferred into the bacterium DH5α. After replication, recombinant plasmids were extracted, digested by the restriction enzyme (Nde I and Hind III) and sequenced. The correct recombinant prokaryotic expression vector was named as pMD18-T-Npm2.

Recombinant protein expression and purification

Expression of recombinant protein in E.coli BL 21 (DE3) and pG-TF2 expression strains followed with the transformation of the recombinant plasmid, pCold II-Npm2. The transformants were cultured in 3 mL of LB medium containing 50 μg/mL ampicillin and grew overnight at 37°C and centrifuged at 3.5×g until the optical density (OD600) of the cultured cells reached 0.5-0.6. Expression of the recombinant protein was induced with 0.5 mM isopropyl-β-D-thiogalactopyranoside (IPTG) at 37°C for 3 h or 0.1 mM IPTG at 16°C overnight, and identified on 15% SDS-PAGE.

The transformants of the recombinant plasmid, pCold II -Npm2 were cultured in 100 mL of LB medium containing 50 μg/mL ampicillin and grown overnight at 37°C. In the next step, it was transferred to 1 L XY1 medium containing 50 μg/mL ampicillin, and incubated until the optical density (OD600) of the cultured cells reached 2.0. Expression of the recombinant protein was induced with 0.5 mM IPTG at 37°C for 3 h and harvest bacteria liquid.

A chelating SFF Ni column was equilibrated with buffer medium containing 50 mM Tris, 500 mM NaCl (pH8.0), gradient eluted with medium containing 50 mM Tris, 500 mM NaCl, 500 mM Imidazole (pH8.0) and dialyzed with 20 mM PB, 500mM NaCl (pH7.4) after elution. Recombinant protein was concentrated and quantified.

Preparation of donor cells

Fetuses (47 days old) isolated from the 22nd generation in the 133 families of BMI pigs were washed three times with phosphate-buffered saline. After removing the head, limbs, and viscera, the fetuses were minced and digested in Dulbecco’s modified Eagle’s medium (DMEM; Gibco) containing 20% fetal bovine serum (FBS; Hyclone), 1% penicillin-streptomycin, and 1 mg/mL collagenase IV for 4 h at 37°C. The cells were centrifuged at 30×g for 5 min, suspended in DMEM supplemented with 10% FBS and 1% penicillin-streptomycin, and then cultured in a flask until grown to 90% confluence. The cells were then passaged and frozen in DMEM containing 20% FBS and 10% dimethylsulfoxide for future use.

In vitro maturation of oocytes

Porcine ovaries were collected from a local slaughter house (Chenggong Ruide Food Co., Ltd, Kunming, Yunnan Province, China) with the permission to use animal parts for this study. The ovaries were transported to the laboratory at 25-30°C in 0.9 % (w/v) NaCl solution. The oocytes were obtained and cultured using the same method previously described (Wei et al., 2013). Porcine follicular fluid (pFF) was aspirated from 3- to 6-mm follicles of ovaries. The fluid was collected under sterile conditions and stored at -20°C. Prior to use, the follicular fluid was centrifuged at 1500×g for 30 min at 4°C, as described previously (Abeydeera et al., 1998).

Nuclear transfer

SCNT was performed as previously described (Wei et al., 2013). After culturing for 38 h to 42 h, oocytes with expanded cumulus cells were briefly treated with 0.1% (w/v) hyaluronidase and cumulus cells were removed using a fine glass capillary pipette. The oocytes were enucleated by aspirating the first polar body and adjacent cytoplasm using a beveled pipette (approximately 20 mm in diameter) in TLH-PVA (Wei et al., 2013). Fetal fibroblasts of the fourth to ninth passages were used as nuclear donor cells and injected to the peri-vitelline space of the oocytes. Donor cells were fused with the recipient cytoplasts with a single direct current pulse of 200 V/mm for 20 msec using an embryonic cell fusion system (ET3, Fujihira Industry Co. Ltd., Tokyo, Japan) in fusion medium (Wei et al., 2013). The reconstructed embryos were cultured and activated with a single pulse in an activation medium (Wei et al., 2013). The reconstructed embryos were equilibrated in PZM-3 supplemented with 5 mg/mL cytochalasin B for 2 h at 38.5°C in humidified atmosphere of 5% CO2, 5% O2, and 90% N2 (APM-30D, ASTEC, Japan).

Injection of remodeling factors

The SCNT-injection manipulation chamber contained a small drop (10 mL) of injection buffer (IB=70 mM KCl, 20 mM HEPES; pH 7.0) with (Npm or PGA) or without (control) remodeling factor. An injection tip approximately 8 mm diameter at the orifice was placed into the drop containing three different concentrations of Npm and four concentrations of PGA in IB. Approximately 0.4 nL remodeling factor was allowed to flow into the oocyte cytoplasm. Since the concentration of Npm in Xenopus egg extract was approximately 500 ng/μL (Mills et al., 1980), Npm was injected to an estimated final concentration of 560 ng/μL (1,680 ng/μL stock solution), 250 ng/μL (750 ng/μL stock solution), or 100 ng/μL (300 ng/μL stock solution). PGA was injected to an estimated final concentration of 100 ng/μL (300 ng/μL stock solution injected), 500 ng/μL (1,500 ng/μL stock solution), 1,000 ng/μL (3,000 ng/μL stock solution), or 2,500 ng/μL (7,500 ng/μL stock solution).

Culture of embryos

Reconstructed embryos were cultured in PZM-3 medium and then placed in an incubator supplied with 5% CO2, 5% O2, 90% N2 at 38.5°C in a humidified atmosphere. Cleavage and blastocyst formation were recorded on days 2 and 7, respectively. Cell numbers of blastocyst were carried out after staining with 10 mg/mL Hoechst 33342 under a laser scanning confocal microscope (TCS SP5II, LEICA, Germany).

RESULTS

Recombinant protein

The synthesized nucleotides sequence encoding Npm2 was amplified by PCR and detected by 2% agarose gel electrophoresis. The location of the resulting DNA fragment is about 660bp on an agarose gel (Fig. 1). Subsequently, the PCR product was ligated into the pMD18-T vector and transformed into the competent E. coli DH5α cells. The clone was identified by PCR and restriction analysis, and then a positive clone was sequenced and the result confirmed the Npm2 gene in frame with C-terminal His6 tag in the pMD18-T multiple cloning sites.

The confirmed recombinant vector was transformed into E. coli BL21 (DE3) cells and pG-TF2. In order to make the recombinant protein expressed maximally, we compared the expression conditions as described in “Materials and Methods”. SDS-PAGE result showed that the recombinant plasmid pCold II-INPM2 were transformed into BL21 (DE3) expression strains and induced with 0.5 mM IPTG at 37°C for 3 h or 0.1 mM IPTG at 16°C overnight. Correct recombinant protein with molecular weight of 32 kDa was obviously expressed in the transformed E. coli BL21 (DE3) cells (Fig. 2A, B) and this protein was almost absent transformed into pG-TF2 expression strains (Fig. 3 A, B).

As shown in Figure 4, recombinant protein containing His6tag was separated and purified by chelating SFF (Ni) column. Recombinant protein product was obtained by dialyzing and concentrating and protein purity was 90% by SDS-PAGE detection (Fig. 5). Finally, the protein concentration we obtained was 1680 ng/μL.

Statistical analysis

An analysis of variance (ANOVA, PROC GLM) was performed using the SAS statistical package (SAS Institute Inc., Cary, NC, USA). All percentage data were subjected to arcsine transformation before statistical analysis. P<0.05 was considered to be statistically significant.

Table I.- Effect of different exogenous Npm or PGA on the efficiency of BMI somatic cell nuclear transfer.

Concentration (ng/μL)	Replicate	Oocytes	Cleavage rate (%)	Blastocyst rate (%)	Cell numbers of blastocyst
560 (Npm)	3	103	71.88±9.28a	25.29±6.36a	42.33±2.52a
250 (Npm)	3	108	76.71±7.71a	16.51±6.37ab	34.67±1.15ab
100 (Npm)	3	115	78.08±6.13a	18.82±4.94ab	35.00±2.65ab
2500 (PGA)	3	71	68.71±7.60ab	11.79±4.28bc	29.67±4.04b
1000 (PGA)	3	74	72.97±3.10a	17.41±2.13ab	27.00±7.07b
500 (PGA)	3	72	57.46±4.29b	11.91±4.12bc	29.00±8.19b
100 (PGA)	3	69	56.97±6.08b	6.82±3.10c	30.56±1.90b
Control	6	182	72.06±6.58a	13.84±5.66bc	34.00±7.21ab

Npm, nucleoplasmin; PGA, polyglutamic acid; BMI, Banna Mini-pig Inbred Line.

Data are expressed as mean±S.D. a, b, c Values with different superscript letters within a column differ significantly (P<0.05).

Effect of exogenous Npm or PGA on the developmental competence of somatic cell nuclear transfer embryos in BMI pig. The developmental competence of BMI somatic cell nuclear transfer embryos injected with exogenous Npm or PGA are summarized in Table I.

The results showed that the cleavage rate of embryos injected with 500 ng/μL and 100 ng/μL PGA were significantly lower than those of other groups (P<0.05). No significant differences were observed in other groups (P>0.05). The blastocyst rate in the 560 ng/μL Npm injected group was significantly higher than those injected with 2500 ng/μL, 500 ng/μL, 100 ng/μL PGA groups and control group (P<0.05). Moreover, the blastocyst rate was highest in the 560 ng/μL Npm injected group (25.29±6.36%) and was lowest in the 100 ng/μL PGA injected group (6.82±3.10%). Cell numbers of blastocysts injected with different concentration of PGA groups were significantly lower than those injected with 560 ng/μL Npm group (P<0.05).

DISCUSSION

Nucleoplasmin is the most abundant protein in the nucleus of Xenopus laevis oocytes, and its molecular mass is about 30 kD and forms a stable pentamer in vivo (Earnshaw et al., 1980). Npm could promote in vitro nucleosome formation, also participate in the decondensation process that the highly compacted sperm chromatin undergoes after fertilization (Loyola and Almouzni, 2004). Similarly, if somatic cell nuclei are injected into the cytoplasm of an egg, for instance during cloning procedures, they also underwent a remodeling process that results intranscriptional reprogramming of the transplanted nucleus (Wade and Kikyo, 2002). In the mouse, three Npm proteins have been identified. Mammalian NPM2 is crucial for histone deacetylation and heterochromatin formation surrounding nucleoli in oocytes and early zygotes (Burns et al., 2003).

Eukaryotic expression systems are frequently employed for the production of recombinant proteins as therapeutics as well as research tools. However, the most appropriate vector and host system must be carefully considered for eukaryotic expression systems. In addition, eukaryotic expression is much more complex and often relies on various feedback mechanisms, developmental processes and environmental factors. Prokaryotic expression systems are widely used because it is simple and effective. In this study, we chose pMD18-T vector to facilitate the following purification. This vector carried a C-terminal His6-Tag, thus, the recombinant protein of Npm should carry a His6 fragment in its C-terminus. The comparatively high level of expression could be achieved with 0.5 mM IPTG at 37°C for 3 h or 0.1mM IPTG at 16°C overnight. At the best expression condition, cells of E. coli BL21 transformed with recombinant vector could produce a recombinant protein of 32 kDa. The molecular weight of the resulting protein was inconsistent with the theoretical value (about 30 kDa) calculated from sequence of the recombinant protein. It can be used to latter experiment.

The data presented in this manuscript suggested that both Npm and PGA could facilitate the in vitro development of porcine NT embryos. The ability of nucleoplasmin to decondense sperm is shared by other highly charged polyanionic molecules such as polyglutamic acid, but only nucleoplasmin can cause decondensation at a physiological rate and at a physiological concentration (Philpott et al., 1991; Ohsumi and Katagiri, 1991). The physiological concentration of Npm found within cytoplasmic extracts derived from activated Xenopus eggs was 500 ng/μL (Philpott and Leno, 1992).The acidic polyanion, PGA, could also mediate sperm decondensation and nucleosome assembly in vitro (Dean, 1983). However, in spite of the fact that PGA has a greater overall negative charge than Npm, remodeling of sperm chromatin requires a higher concentration of PGA than Npm (Philpott et al., 1991). Previous studies showed that addition of chromatin remodeling factors to the bovine oocytes may improve development of NT embryos by facilitating reprogramming of the somatic nucleus (Betthauser et al., 2006).

In our studies, the results showed that injection of 560 ng/μL exogenous Npm could improve the blastocyst rate of NT embryos in BMI. Its concentration was similar to the physiological concentration of Npm derived from activated Xenopus laevis eggs. This may be because of exogenous injection Npm upregulating gene expression related to embryo development and reflecting a global depression of transcription associated with Npm-driven remodeling of somatic chromatin (Betthauser et al., 2006). This remodeling might include the removal of somatic histone H1 and other linker-binding proteins from chromatin (Ramos et al., 2005), and/or facilitated transcription factor binding concomitant with the removal of nucleosome core particles from the DNA (Chen et al., 1994). Compared with injection of Npm, injection of PGA at 1000 ng/μL could improve the developmental ability of BMI pig NT embryos. However, injecting a high concentration of PGA decreased the developmental competence of NT embryos. This result was similar to previous studies (Betthauser et al., 2006). This may be due to a remodeling factor-dependent developmental ‘‘threshold’’ and concentrations of Npm above this threshold facilitate blastocyst development, while similar concentrations of PGA inhibit development (Betthauser et al., 2006). These results may indicate that Npm and PGA operate through different mechanisms even though Npm contains several acidic tracts within its structure (Dingwall and Laskey, 1990; Prado et al., 2004), and PGA can mimic Npm’s decondensation and nucleosome core assembly activities in vitro (Dean, 1983). However, Npm-dependent chromatin remodeling does not appear to be mediated through its acidic tracts alone. So, the mechanism of Npm expression, regulation and function need to be further studied.

CONCLUSION

In conclusion, we successfully obtained the recombinant nucleoplasmin by prokaryotic expression system. Moreover, addition of recombinant Npm or PGA could further improve the development of SCNT embryos in the BMI pig. Further studies will be required to understand the mechanism of Npm expression and regulation.

ACKNOWLEDGEMENTS

This study was supported by the National Natural Science Foundation of China (Grant No. 30800785). These authors are grateful to Professor Peter M Jobst (Virginia Polytechnic Institute and State University) for their critical reading and comments on this manuscript.

Statement of conflict of interest

The authors declare that there is no conflict of interest.

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