Molecular characterization of MHC-DRB cDNA in water buffalo (Bubalus bubalis)

Molecular characterization of MHC-DRB cDNA in water buffalo (Bubalus bubalis)

Soumen Naskar^I; Sitangsu M. Deb^II; Saket K. Niranjan^III; Subodh Kumar; Deepak Sharma^IV; Durgam Sakaram^V; Arjava Sharma^VI

^INational Research Centre on Pig, Guwahati, Assam, India

^IICentral Arid Zone Research Institute Regional Research Station, Pali-Marwar, Rajasthan, India

^IIINational Bureau of Animal Genetic Resources, Karnal, Haryana, India

^IVPt. Deen Dayal Upadhayaya Veterinary and Animal Sciences University, Mathura, Uttar Pradesh, India

^VSri Venkateswara Veterinary University, Hyderabad, Andhra Pradesh, India

^VIProject Directorate on Cattle, Meerut, Uttar Pradesh, India

^{Send correspondence to}

ABSTRACT

In the present study, water buffalo MHC (Bubu)-DRB cDNA was cloned and characterized. The 1022 base long-amplified cDNA product encompassed a single open reading frame of 801 bases that coded for 266 amino acids. The Bubu-DRB sequence showed maximum homology with the BoLA-DRB3*0101 allele of cattle. A total of seven amino acid residues were found to be unique for the Bubu-DRB sequence. The majority of amino acid substitutions was observed in the β₁ domain. Residues associated with important functions were mostly conserved. Water buffalo DRB was phylogenetically closer to goat DRB*A.

Key words: water buffalo, cDNA, DRB, MHC, phylogeny.

The major histocompatibility complex (MHC) plays a central role in the processing and presentation of antigens, and in discriminating between self and non-self. MHC class II molecules, after selectively binding different peptides derived from exogenous pathogens, present them to helper T cells (Brown et al., 1993). MHC class II molecules, located primarily on the surface of antigen-presenting cells, are heterodimer glycoproteins composed of two polymorphic transmembrane polypeptide chains, termed α and β. The DRB genes under the DR region of the MHC complex encode for the highly polymorphic β-chain (Ellis and Ballingall, 1999). Three bovine DRB genes have been reported. Of these, DRB3 appears to be highly expressed, DRB1 is a pseudogene, and DRB2 is transcribed at a very low level in lymphocyte tissues (Lewin et al., 1999). An extremely polymorphic second exon of the DRB gene encodes those peptide binding sites (PBS) responsible for antigen binding (Rask et al., 1985). Currently, more than 100 alleles of the DRB3 gene have been described (BoLA Nomenclature, ISAG; EMBL-EBI) in Bos taurus and Bos indicus cattle. Importantly, besides its association with several diseases, polymorphism at the DRB exon 2 region is also considered a potential candidate-marker gene.

Riverine buffalo (Bubalus bubalis), well adapted to a hot and humid tropical climate, seems to tolerate many common infectious diseases. Although already mapped on chromosome 2 (Rodrigues et al., 2008), water-buffalo MHC has been little studied, with the scarcity of data regarding diversity (De et al., 2002, Sena et al., 2003, Niranjan et al., 2009). Herein, DRB genes expressed in water buffalo were cloned and characterized.

Venous blood was collected from a randomly selected and healthy Indian Murrah water buffalo. Total RNA was extracted from a lymphocyte culture with total RNA minipreps super kit (Biogene, USA). RT-PCR was carried out with a RevertAid first strand cDNA kit (MBI Fermentas). Both strands of DRB cDNA were produced by PCR, using Forward - 5'-GACTTGCCTGCTCCTCTCAC TCTC-3' and Reverse - 5'-AGGGTGGGGGTGACTGAG AAAAC-3' primers, with design based on the cattle DRB3 sequence (Accession No. AY125893). PCR amplification was in a total volume of 25 µL with 6 µL of first strand cDNA, 1x PCR buffer, 1.5 mM of MgCl₂, 200 µM of each dNTPs, 30 pmol of each primer and 1 unit of Taq DNA polymerase. The polymerase chain reaction (PCR) was carried out in a thermal cycler (DNA Engine PTC200, M.J. Research) under the following conditions: initial denaturation at 94 °C for 3 min, followed by 35 cycles of 94 °C for 1 min, 60 °C for 1 min and 72 °C for 1.5 min, and a final extension at 72 °C for 10 min. The amplified cDNA product of DRB was purified using the QIAquick gel extraction kit (Qiagen). The purified product was ligated into a pGEM-T Easy vector system (Promega). After confirmation by colony PCR, and the release of inserts from plasmids by digestion with EcoRI, positive clones were subjected to double stranded sequencing by primer walking in an automated DNA sequencer. The obtained sequence was annotated and submitted to NCBI GenBank (Acc. no. DQ057985). The nucleotide and deduced amino acid sequences of water buffalo DRB cDNA were compared with those from other species.

Based on the DRB cDNA sequences of the water buffalo and other species, the neighbor-joining method together with the MEGA 4 programme (Tamura et al., 2007) was applied for defining a phylogenetic tree. Bootstrap values were obtained using 500 replicates. Evolutionary divergence (base substitution/site) was computed by the bootstrap procedure (500 replicates) using the Kimura 2-parameter method based on a nucleotide model (Kimura, 1980) from the MEGA 4 programme (Tamura et al., 2007).

The amplified 1022-nucleotide-long cDNA sequence of the water buffalo DRB gene contained the complete coding region of 801 nucleotides. The annotated Bubu-DRB sequence was highly similar to orthologous DRB sequences of other species. Homology with various cattle alleles varied between 89.9% (BoLA-DRB3*3101) and 92.1% (BoLA-DRB3*0101). Homologies with sheep, goat, pig and human alleles were 89.8, 89.1, 77.5 and 79%, respectively.

The resultant Bubu-DRB amino acid sequence was 266 amino acids long. Six exons encoding six different domains, a characteristic feature of MHC class II molecules, were confirmed (Russel et al., 1997). The sizes of various domains, viz., signal peptide, β₁, β₂, connecting peptide (CP), transmembrane (TM) and cytoplasmic (CY) domains, were analogous to the DRB sequences of other species (Figure 1). A total of seven amino acid residues (3, 29, 66, 79, 150, 153 and 227) were unique to the Bubu-DRB sequence, six of which were otherwise highly conserved. Importantly, one of the residues (position 66) was associated with an antigen binding site (ABS). When compared with the closest cattle allele, DRB3*0101, 20 residue substitutions with maximum numbers (11) in the β₁ domain of Bubu-DRB were observed. The water buffalo sequence showed 22, 26, 57 and 51 residue-differences with those of sheep, goats, pigs and humans, respectively. As expected, most of the substitutions were observed in the β₁ domain when compared across species. Alleles at the BoLA-DRB3 locus gave evidence of over-dominant selection, with the peptide binding site (PBS) region presenting a higher proportion of mutations compared to non-PBS regions (Sena et al., 2003).

169 residues (SP-13, β₁-49, β₂-70, CP-8, TM-15 and CY-14) were noted to be completely conserved across the species. Among these, 49 were found to be specific to ruminants, but not to pig and human. Out of the 24 residues associated with ABS (Brown et al., 1993), in water buffalo, 17 were found to be conserved, and those at positions 40, 42, 61, 66, 100, 107 and 115 to be different. Valine (115), essential in creating a deep pocket at PBS surrounded by predominantly nonpolar residues of both the α₁ and β₁ domains, was found substituted by phenylalanine in water buffalo. Interspecies variability of this residue is great. The dominant 'anchoring' peptide residue binds to the hydrophobic pocket of Phe (115), along with α₂₆ and α₃₁. One of the residues (84) associated with CD4 binding (Brown et al., 1988), was found to be substituted in water buffalo DRB. Highly conserved Asn (111), which supposedly forms the hydrogen bond through its Γ amide group with the main chain peptide, was invariant in water buffalo. Mutation at this position affects intracellular transport and cell-surface expression of class II molecules in mice. Similarly, the residue Trp (90), apparently conserved across species, is placed in such a way that its indole nitrogen is capable of donating a hydrogen bond to the main chain carbonyl group of a bound peptide, in exact homology to the location and function of Trp (147) of class I. Polymorphic residue Asp (86) forms a salt bridge with a conserved Arg (76) of the α chain under the existing peptide (Nydam et al., 1998). This residue (β₅₇) of HLA-DQ has been found associated with insulin-dependent diabetes mellitus (IDDM) in humans (Brown et al., 1993). In addition to any possible effect on peptide binding, polymorphism at this residue may affect either the stability or structure of the αβ heterodimer, since nearby residues Glu (81) and Arg (84) form part of the interface of the dimer (Brown et al., 1988).

Two salt bridges from Glu (81) to Arg (84) on the neighboring molecule are conserved in HLA-DR1, which forms the first of four interfaces between DR1 molecules in dimers. However, residue Arg (84) was found to be substituted by Gln in water buffalo. Three more salt bridges, i.e., His (140), Glu (191) and His (141) of the β₂ domain, with the α₂ domain residues Glu (158), His (177) and Glu (179), respectively, were found to be conserved across the species. The T-cell coreceptor molecule, CD4, is thought to bind to the residues, Gln (139), Glu (166), Ala (169), Gly (170) and Val (171). With the exception of residue Ala (169) in humans (Ala → Thr), total conservation across species was observed in these positions. Apart from a partial affinity for Gln (139), residues Gly (170) and Val (171) are very important for CD4 binding.

In the mechanism by which MHC molecules tightly bind several peptides, the role of clusters of conserved residues in the class II molecules, Trp (91) (except Arg in pig) and Asn (111) (along with α₆₂ Asn, α₆₉ Asn and α₇₆ Arg), are spaced so as to bind at intervals to the extended main chain of bound peptides, thereby providing an independent peptide side chain component to the affinity (Brown et al., 1988). The disulphide linked Cys residues at positions 44 and 108 of the β₁ domain, and at positions 146 and 202 of the β₂, were conserved across species. The N-glycosylation region, or the -CHO site at residue positions 48-50 (Asn-Gly-Thr), was completely conserved in all the species compared.

Phylogenetic analysis based on complete cDNA using the Neighbor-Joining method (Nucleotide: Kimura 2-parameter model), revealed the gathering of several ruminant DRB alleles into a single group (Figure 2). The clustering of different ruminant sequences along with those of water buffalo seems to have arisen from trans-species evolution, a feature common to MHC genes, where the clusters had possibly ensued from primordial sequences in a common ancestor (Klein, 1986). Similarly, the sharing of common types of pathogens among the ruminants is also indicated (Hickford et al., 2004). Nevertheless, Bubu-DRB seems to be closer to the goat DRB sequence than to those of cattle. Evolutionary divergence of Bubu-DRB based on base substitution per site was the lowest (0.036) with BoLA-DRB3*0101 (0.036) and the highest (0.139) in pig (Table 1).

Thus, it is apparent that Bubu-DRB is expressed, and that there is considerable similarity with other ruminant species, not only as to cDNA sequences, but also functionally important conserved residues. Nevertheless, high genetic variation corresponding to the exon 2 region of cDNA, possibly supplementary to antigen repertoire properties, was revealed.

Acknowledgments

The authors wish to thank the Director of the Indian Veterinary Research Institute, Izatnagar, for the use of facilities. Financial assistance provided by the Department of Biotechnology (Government of India) is duly acknowledged.

Internet Resources

Received: July 13, 2011

Accepted: October 26, 2011.

Associate Editor: Bertram Brenig

License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Animal Genetics Division, Indian Veterinary Research Institute, Izatnagar, Uttar Pradesh, India

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Publication Dates

• Publication in this collection
  02 Feb 2012
• Date of issue
  2012

History

• Received
  13 July 2011
• Accepted
  26 Oct 2011