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Int J Biol Sci 2007; 3(7):428-433. doi:10.7150/ijbs.3.428 This issue Cite

Research Paper

cDNA Cloning and Overexpression of Acidic Ribosomal Phosphoprotein P1 Gene (RPLP1) from the Giant Panda

Yu-Jie Du¹, Xiao-Yan Luo², Yan-Zhe Hao¹, Tian Zhang¹, Wan-Ru Hou¹

1. College of Life Science, China West Normal University, 44# Yuying Road, 637002, Nanchong, China
2. Northwest Plateau Institute of Biology, the Chinese Academy of Sciences, 59# Xinning Road, 810001, Xining, China

Abstract

RPLP1 is one of acidic ribosomal phosphoproteins encoded by RPLP1 gene, which plays an important role in the elongation step of protein synthesis. The cDNA of RPLP1 was cloned successfully for the first time from the Giant Panda (Ailuropoda melanoleuca) using RT-PCR technology, which was also sequenced, analyzed preliminarily and expressed in E.coli. The cDNA fragment cloned is 449bp in size, containing an open reading frame of 344bp encoding 114 amino acids. Alignment analysis indicated that the nucleotide sequence and the deduced amino acid sequence are highly conserved to other five species studied, including Homo sapiens, Mus musculus, Rattus norvegicus, Bos Taurus and Sus scrofa. The homologies for nucleotide sequences of Giant Panda PPLP1 to that of these species are 92.4%, 89.8%, 89.0%, 91.3% and 87.5%, while the homologies for amino acid sequences are 96.5%, 94.7%, 95.6%, 96.5% and 88.6%. Topology prediction showed there are three Casein kinase II phosphorylation sites and two N-myristoylation sites in the RPLP1 protein of the Giant Panda (Ailuropoda melanoleuca). The RPLP1 gene was overexpressed in E. coli and the result indicated that RPLP1 fusion with the N-terminally His-tagged form gave rise to the accumulation of an expected 18kDa polypeptide, which was in accordance with the predicted protein and could also be used to purify the protein and study its function.

Keywords: cDNA cloning, overexpression, RPLP1, acidic ribosomal phosphoprotein P1, the Giant Panda (Ailuropoda melanoleuca)

1. Introduction

Ribosome, a compact ribonucleoprotein (RNP) grain that catalyzes protein synthesis, consists of 4 RNA species and approximately 80 structurally distinct proteins [1, 2]. It can be dissociated into a small subunit and a large one whose shape and structure are irregular and asymmetric. The large ribosomal subunit has a distinct lateral protuberance called the stalk, which is an important and essential structure involved directly in the interaction of the elongation factors with ribosome during protein synthesis [3, 4]. In Saccharomyces cerevisiae, the ribosomal stalk is made of five components, the 32kDa P0 and four 12kDa acidic proteins, P1alpha, P1beta, P2alpha and P2beta [5]. These proteins are called A-proteins (acidic) or P-proteins (the phosphorylated eucaryotic A-proteins), which are generally present in multiple copies on the ribosome and have isoelectric points in the range of pH 3 to 5, in contrast to most ribosomal proteins which are single copy and basic [6].

There is only one type acidic protein in prokaryotes while two protein families are found in eukaryotes, phosphoproteins P1 and P2, which presumably have different roles and interact with each other participating in protein synthesis [7, 8]. The acidic ribosomal phosphoprotein P1 (RPLP1) is internally located while RPLP2 is more external in the stalk and the interaction between RPLP1 and RPLP2 is necessary for forming the stalk structure [7, 9-13]. RPLP1, also known as P1, RPP1, MGC5215, FLJ27448, is one of components constituting the large ribosomal subunit and is located in the cytoplasm. Together with RPLP0, RPLP2 and the conserved domain of 28S rRNA, it constitutes a major part of the GTPase-associated center in eukaryotic ribosomes [14, 15]. In addition, it can attach to ubiquitin and assists the ubiquitin in regulating numerous important cellular processes including apoptosis, transcription, and the progression of cell cycle [16].

RPLP1 gene was cloned and studied from many animals including Homo sapiens [17-19], Mus musculus [20], Rattus norvegicus [21, 22], Gallus gallus [23], Danio rerio [24], Bos Taurus [25], Anopheles gambiae [26], Drosophila melanogaster [27], Bombyx mori [28] etc. However, RPLP1 gene from the Giant Panda (Ailuropoda melanoleuca) has not been reported yet.

The Giant Panda living on the arrow bamboo is a rare species currently found only in China and has been endangered due to climatic changes and past hunting activities. Its population originally extended throughout most of southern and eastern China, northern Myanmar and northern Vietnam. But now it is limited to the west and the north of Sichuan province, the south of Gansu province, eastern Tibet and the southwest of Shanxi province. It is one of declining wild lives in the world and studies on it are increasingly concerned by the world community. For many years, studies on the Giant Panda have been mainly concentrated on fields such as breeding and propagation, ecology, morphology, taxology, physiology and pathological biochemistry. Recently, researches on the Giant Panda have been undergoing a change from the level of cell (mainly the chromosome level) to molecule. Most studies have focused on genetic diversity, parentage and phylogenesis etc, while reports on functional gene are handful [29-34]. It would further our understanding of this rare species by molecular studies of genes such as RPLP1.

This study was conducted using RT-PCR technique to amplify the cDNA sequence of RPLP1 gene from the total RNAs extracted from the skeleton muscle of the Giant Panda, and then analyzed the sequence characteristics of the protein encoded by the cDNA and compared it with those of human and other mammalian species reported. We also overexpressed it in E. coli using pET28a plasmids. The study provides scientific data for inquiring into the hereditary traits of the gene from Giant Panda and formulating the protective strategy for the Giant Panda.

2. Materials and methods

Materials and RNA isolation

Skeletal muscle was collected from a dead giant panda at the Wolong Conservation Center of the Giant Panda, Sichuan, China. The collected skeletal muscle was frozen in liquid nitrogen and then used for RNA isolation.

Total RNAs were isolated from about 400mg of muscle tissue using the Total Tissue/Cell RNA Extraction Kits (Waton Inc., Shanghai, China) according to the manufacturer's instructions. The total RNAs extracted were dissolved in DEPC (diethypyrocarbonate) water, and kept at -70°C.

Primers Design, RT-PCR, Cloning of RT-PCR Products and Sequencing

The PCR primers were designed by Primer Premier 5.0, basing on the mRNA sequence of RPLP1 from Homo sapiens (BC003369), Mus musculus (BC058685), Rattus norvegicus (BC058151), Sus scrofa (DQ629169) and Bos taurus (BC102695). The specific primers of RPLP1 are as follows: RPLP1-F: 5′-CTTCCGAGGAAGCTAAGGCCGCGTT-3′; RPLP1-R: 5′-AGAGGTTTAGTCAAAAAGACCAAAG-3′.

Total RNAs were synthesized into the first-stranded cDNAs using a reverse transcription kit with Oligo dT as the primers followed by PCR amplification according to the manufacturer's instructions (Promega). After amplification, PCR products were separated by electrophoresis in 1.5% agarose gel with 1× TAE buffer, stained with ethidium bromide and visualized under UV light. The expected fragments of PCR products were harvested and purified from gel using a DNA harvesting kit (Omega, China), and then ligated into a pUC18 vector at 22°C for 12 hours. The recombinant molecules were transformed into E. coli complete cells (JM109), and then spread on the LB-plate containing 50μg/mL ampicillin, 200mg/mL IPTG and 20mg/mL X-gal. Plasmid DNA was isolated and digested by PstI and ScaII to verify the insert size. Plasmid DNA was sequenced by Huada Zhongsheng Scientific Corporation (Beijing, China).

Construction of the Expression Vector and Overexpression of Recombinant RPLP1

PCR fragment corresponding to the RPLP1 polypeptide was amplified from the RPLP1 cDNA clone with the forward primer, 5'-TCT GGA TCC CTC GCC CGC ACC ATG -3' (BamHI) and reverse primer, 5'- CTC AAG CTT TTA GTC AAA AAG ACC AA-3' (HindIII), respectively. The PCR was performed at 94°C for 2 minutes; 35 cycles of 30s at 94°C, 45s at 55°C and 1 minute at 72°C; 7 minutes at 72°C. The amplified PCR product was cut and ligated into corresponding site of pET28a vector (Stratagen). The resulting construct was transformed into E.coli BL21(DE3) strain (Novagen) and used for the induction by adding IPTG (isopropyl-b-D-thiogalactopyranoside) at an OD600 of 0.6 and culturing further for 5 hours at 37°C, using the empty vector transformed BL21(DE3) as a control. The recombinant protein samples were induced after 1, 2 and hours, and then separated by SDS-PAGE (27) and stained with Coomassie Brilliant Blue dye.

Data analysis

The sequence data were analyzed by GenScan soft­ware (http://genes.mit.edu/GENSCAN.html). Homology research of the Giant Panda RPLP1 com­pared with the gene sequences of other species ware performed using Blast 2.1 (http://www.ncbi.nlm.nih.gov/blast/). ORF of the DNA sequence was searched using ORF finder soft­ware (http://www.ncbi.nlm.nih.gov/gorf/gorf.html). Protein structure of the RPLP1 sequence cloned was deduced using PredictProtein software (http://cubic.bioc.columbia.edu/predictprotein/).

3. Results and discussion

Analysis of the cDNA of RPLP1 from the Giant Panda

A cDNA fragment of 448bp was amplified from the Giant Panda with primers RPLP1-F and RPLP1-R (Fig. 1). Blast research showed that the cDNA sequence cloned shares a high homology to the RPLP1 from some mammals reported, including Homo sapiens, Mus musculus, Rattus norvegicus, Bos Taurus and Sus scrofa. On the basis of the high identity, we concluded that we had cloned the cDNA encoding the Giant Panda RPLP1 protein. The RPLP1 sequence was submitted to Genbank (accession number: EF631972), containing the 5'- untranslated sequence in size of 97bp and the 3'-untranslated region in size of 7bp. An ORF of 344bp encoding 114 amino acids was found in the cDNA (Fig. 2).

 Fig 1 

Reverse Transcription Polymerase Chain Reaction Products of the Giant Panda RPLP1. M: Molecular ladder DL2000; 1: the amplified RPLP1

Analysis of the homologies for nucleotide sequences and amino acid sequences

The homologies for nucleotide sequences between the Giant Panda and five mammals studied, including Homo sapiens, Mus musculus, Rattus norvegicus, Bos Taurus and Sus scrofa, are 92.4%, 89.8%, 89.0%, 91.3% and 87.5%, and for amino acid sequences are 96.5%, 94.7%, 95.6%, 96.5% and 88.6% (Table 1), respectively. Among them, the Giant Panda shares the highest homology with the nucleotide sequence and amino acid sequence of Homo sapiens. Alignment analysis of RPLP1 among the Giant Panda and the five mammals indicated that the nucleotide sequence and the deduced amino acid sequence are highly conserved (Table 1 and Fig. 3).

 Fig 2 

Nucleotide Sequence of cDNA Encoding the Giant Panda RPLP1 and the Amino Acid Sequence Deduced from Its ORF. Nucleotides are numbered in the 5'-to-3' direction. The predicted amino acid sequence of the gene is shown under the nucleotide.

 Fig 3 

Comparison of the Amino Acid Sequence of RPLP1 Among the Giant Panda, Homo sapiens, Mus musculus, Rattus norvegicus and Bos Taurus. Sus: Sus scrofa; rat: Rattus norvegicus; bos: Bos Taurus; homo: Homo sapiens; mus: Mus musculus; panda: the Giant panda; __: casein kinase II phosphorylation site; ‗‗: N- myristoylation site

Prediction and analysis of protein functional sites in RPLP1 protein

Topology prediction revealed three N-glycosylation sites and two Casein kinase II phosphorylation sites in the RPLP1 protein. Our analysis indicated that there are three Casein kinase II phosphorylation sites and two N-myristoylation sites in the same locations in RPLP1 protein of the Giant Panda, Homo sapiens, Rattus norvegicus and Bos Taurus. Thus, in contrast with the topology prediction, there is one more N-myristoylation site in the RPLP1 from Mus musculus spanning amino acids 79-84 and one less N-myristoylation site in the RPLP1 from Sus scrofa spanning amino acids 57-62.

Further analysis detected 15 polymorphic sites in the amino acid sequences of the six species compared. Among these polymorphic sites, four amino acid residues in the RPLP1 of the Giant Panda are different from those of Homo sapiens and other four mammals. These distinctive sites are respectively I (Ile) at the fifty-fourth site, T (Thr) at the eighty-fifth site, D (Asp) at the hundredth site, H (His) at the one hundred-fifth site. All the four distinctive sites result from the transversion or transition of the corresponding codons, but there is not any deletion and insertion of bases. Among the four distinctive sites, the one at the hundred-fifth site is located in a casein kinase II phosphorylation site, but it does not result in any differences from human and other four mammalian species in the functional site. The fact shows that the variation of sites has no affect on the structure and function of RPLP1 protein. However, what changes caused by other mutations outside the functional sites in the structure and the function of RPLP1 protein are poorly understood and further studies need conducting.

It was reported that the carboxy-terminal 17-amino-acid sequence KEESEESD(D/E)DMGFGLFD of RPLP1 protein is the basis of its immunological cross-reactivity [17, 35]. But for the RPLP1 protein from the Giant Panda, the 17-amino-acid sequence is KEDSEESHDDMGFGLFD. Within the area, there are two mutation sites, which have been underlined. One located at the one hundred-fifth site in a casein kinase II phosphorylation site changes from E to D, which is caused by its corresponding codon changing from GAT to CAT; the other one located at the hundredth site outside functional sites changes from D to H, which is caused by its corresponding codon changing from GA(A/G) to GAC. Further research needs to be conducted to explain whether the two mutation sites will lead to changes in the basis of its immunological cross-reactivity.

Prediction of the physical and chemical features of RPLP1 protein

The molecular weight of the RPLP1 protein from the Giant Panda is 11.566kDa and the theoretical pI is 4.40. Further analysis showed the molecular weight and theoretical pI of the putative protein among the Giant Panda and the five mammalians studied are very close (Table 2).

Overexpression of the RPLP1 gene in E. coli

Next, we intended to overexpress the RPLP1 gene in E. coli using pET28a plasmids carrying strong promoter and terminator sequences derived from phage T7. For this purpose, the RPLP1 gene was amplified individually by PCR and cloned in a pET28a plasmid, resulting in a gene fusion coding for a protein bearing a His-tag extension at the N terminus. Expression was tested by SDS-PAGE analysis of protein extracts from recombinant E. coli strains BL21 (Fig. 4). Data showed that the protein RPLP1 fusion with the N-terminally His-tagged form gave rise to the accumulation of an expected 18 kDa polypeptide that formed inclusion bodies. Apparently, the recombinant protein was expressed after half an hour of induction and then after 2 hours reached the highest level. These results suggested that the protein is active and it is just the protein encoded by the RPLP1 from the Giant Panda. The expression product obtained could be used to purify the protein and study its function further.

 Fig 4 

Protein extracts from recombinant E. coli strains were analyzed by SDS-PAGE gel stained with Coomassie blue. Numbers on right show the molecular weight, and the arrow indicates the recombinant protein bands induced by IPTG with 0, 0.5, 1, 2 and 4 hours (lane 1-5), respectively.

In Summary, the complete coding sequence of RPLP1 gene has been cloned using RT-PCR technology and the expression experiment in E.coli has been performed successfully. This is the first report on the RPLP1 gene from the Giant Panda. The data will not only enrich and supplement the information about RPLP1 but also allow the isolation of the structural gene from the Giant Panda. Further research on PRLP1 protein is desirable with a view of inquiring into the physiological function of the stalk structure. In addition, it will contribute to the protection for gene resources and the discussion of the genetic polymorphism of this “Treasure of China”, yet endangered species.

Acknowledgements

This work is supported by the Key Chinese National Natural Science Foundation (30470261), Application Technology Project in Sichuan Province (2006J13-057) and Key Discipline Construction Project in Sichuan Province (SZD0420).

Conflict of interest

The authors have declared that no conflict of interest exists.

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Author contact

Correspondence to: Wan-ru Hou, PhD, College of Life Science, China West Normal University, 44# Yuying Road, 637002, Nanchong, China. Phone/Fax: +86-0817-2314311. E-mail: hwr168com.cn.

Received 2007-9-19
Accepted 2007-10-18
Published 2007-10-26

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