Estimating the Distance of Genetic Domestic Goats in Iran Inferred from D-Loop Region of Mitochondrial DNA Analysis and Origins of Candidate Native Goat Ancestor

Research Article

Austin J Vet Sci & Anim Husb. 2018; 5(3): 1048.

Estimating the Distance of Genetic Domestic Goats in Iran Inferred from D-Loop Region of Mitochondrial DNA Analysis and Origins of Candidate Native Goat Ancestor

Mohammadi SB¹*, Afshari KP¹ and Seyedabadi HR²

¹Department of Animal Science, Abhar Branch, Islamic Azad University, Abhar, Iran

²Department of Animal Biotechnology, Animal Science Research Institute of IRAN (ASRI), Agricultural Research Education and Extension Organization (AREEO), Karaj, Iran

*Corresponding author: Mohammadi SB, Department of Animal Science, Abhar Branch, Islamic Azad University, Abhar, Iran

Received: July 25, 2018; Accepted: September 10, 2018; Published: September 17, 2018

Abstract

The wild goat “bezoar” (Capra aegagrus) has been considered to be the strongest candidate for the ancestor of the domestic goats (C. hircus). This article describes the complete sequences of the mitochondrial DNA displacement loop (D-loop) region from Mahabadi goats. The control region (D-loop) is the most variable and non-coding portion of the mitochondrial genome. The genetic diversity and phylogenetic structure was analyzed in Mahabadi goat population by mitochondrial DNA sequences. It is estimated genetic distance between native goat and goat ancestor based on mtDNA. Recent analysis of the most of domestic goat individuals revealed a total of six different monophyletic mitochondrial DNA (mtDNA) haplogroups A, B, C, D, F, and G, with the A haplogroup representing >90% of individuals . Phylogenetic analysis was carried out using hyper variable region 1 (896 bp) obtained form 30 animals. All Mahabadi haplotypes were classified into a haplotype group and revealed remarkably high genetic distances within the population when compared with other goat populations from several places, indicating high genetic variation in the Mahabadi goat. After extracting DNA, displacement loop (D-loop) region of mtDNA was amplified with specific primers using PCR and after purification was sequenced. The phylogenic tree was drawn with the consensus sequence of other similar sequences of different goat’s breeds and wild goat “bezoar” (Capra aegagrus) obtained from GenBank. In the phylogenic tree, Mahabadi native goat was clustered with Switzerland, Romania, Austria, Cyprus, Jordan, Spain, Saudi Arabia, Albania, Turkey, Egypt, Kurdi Iran, Malaysia, Kyrgyzstan, Italya and ancestor of native goat breeds. The findings confirmed that Mahabadi goats was closed to Capra aegagrus compared to other domestic goats.

Keywords: Genetic Diversity; Capra Aegagrus; Mahabadi Goat; mtDNA; Phylogenetic; Genetic Distance

Introduction

Domesticated goats (Capra hircus) are among the most important farm animals in many parts of the world, particularly Africa and Asia. Goats were thought to have been domesticated in the ninth and eighth millennia BC during the Pre-Pottery Neolithic B (PPNB) period, specifically between 8700 and 6800 cal BC in the Zagros Mountains, it is Known for their hardiness, goats have adapted to many different habitats, including savannas, deserts, scrubs and mountain ranges, and are found in all types of ecological environments, particularly in tropical and dry regions, where other livestock species have difficulties surviving [1]. Goats are included in the entire range of production systems, from intensive production to small holders and nomadic human populations, and are raised around the world for their meat, milk, cheese, fiber and hides. Goats are also kept as pets or for entertainment or cultural and religious purposes. Angora goats appear in one color which is white to silver, but Mahabadi goats produce mohair in different natural colors which are a unique character of this breed. Keeping above in view in present study, the current phylogenetic status and genetic diversities of Mahabadi goat has been investigated in order to understand the genetic basis of this breed. Mitochondrial genome (mtDNA) analysis is a critical tool in the fields of evolutionary and population genetics, including molecular. The mitochondrial DNA (mtDNA) polymorphism, especially the displacement loop (D-loop) region, has been largely applied to understand phylogenetical relationships in many animal species, including cattle [2-9] previous studies on domestic goats identified at least four major mtDNA lineages [10-12]. Lineage A is the most diverse and widely distributed across all continents.

This article describes the complete sequences of the mitochondrial DNA displacement loop (D-loop) region from domestic goats and several domestic goat and also native goat ancestor “Capra aegagrus”. The control region (D-loop) is the most variable and non-coding portion of the mitochondrial genome [13]. This region controls the mitochondrial DNA (mtDNA) replication by regulating the activities of various enzymes and proteins that are coded by the nuclear genes [14]. The sequences of the control region vary greatly in different mammalian species, however, preservation of several conserved regions indicate fundamental harmony in its function [15]. Because of their rapid evolution [16], the control region sequences are valuable for investigating the genetic diversity and evolutionary relationships among species [13]. The extent and pattern of genetic variability in livestock species will contribute to the conservation of livestock genetic resources. On the basis of the previously mentioned archaeological studies and bio-geography, it is likely that the molecular studies of diversity in Iranian goats will yield new understanding of the origin and process of goat domestication, and will contribute to the resolution of goat phylogeny. More than 20 breed of goats have been recognized in Iran, these small breeds of goat are distributed over the western and north-west of Iran near to the Turkey and Iraqi borders.

Three wild species of the genus Capra, the bezoar (C. aegagrus), markhor (C. falconeri) and ibex (C. ibex), are closely related to the domestic goat (C. hircus), and it has been suggested that these species contributed to the gene pool of domestic goats, possibly via early translocations of animals and feralization prior to the global spread of goats.

It is now widely agreed that C. aegagrus is the wild ancestor of domestic goats, and this finding has been confirmed by the presence of all “domestic” haplogroups in the current C. aegagrus populations. The bovid known as the Wild Goat (Capra aegagrus) was the progenitor of the Domestic Goat, although domestic goats have probably been hybridized with other wild goat species in Asia. Wild Goats are found in western Asia (since their introduction in 1970, a free-roaming population maintained by hunting at 500 to 1000 individuals has also existed in New Mexico USA). They live in rocky habitats associated with cliffs from sea level to around 4000m (but usually below 2500m). Although in Daghestan they inhabit some montane forests, in general Wild Goats are associated with deserts and semi-arid areas. Natural predators such as Gray Wolves (Canis lupus) and Leopards (Panthera pardus) have been extirpated in most areas now occupied by Wild Goats. The nucleotide sequence data reported in this paper will appear in the GenBank sequence database Capra aegagrus with the accession numbers AB004076.1. Recent analysis of 2,430 domestic goat individuals revealed a total of six different monophyletic mitochondrial DNA (mtDNA) haplogroups A, B, C, D, F, and G, with the A haplogroup representing >90% of individuals. The three goat (C. hircus) mtDNA haplogroups (A, B, and C) found by Luikart et al. (Figure 1) have been interpreted to indicate three distinct domestication events. By comparing the sequence obtained from district HVR1-of-breed goats Mahabad sequences of these six groups of haplotypes as a sequence of reference in the study by Nader et al in 2009 took the form of a table in the study that Mahabadi goats belonging to haplotype group A is based on the analysis (Figure 5).

Assuming a single haplotype domesticated per haplogroup and a coalescence time of 10,000 years for the most common a haplogroup, it was hypothesized that the domestication of B and C haplogroups occurred approximately 2,130 and 6,110 years ago, respectively. This result has been explained by some authors [11,17] because goat, owing to its moderate size and ability to adapt to different environments, well-suited to the intercontinental transportation in ancient times. Based on previous literatures, in this study, molecular analysis of Mahabadi goat population based on D-Loop region of mitochondrial DNA were investigated to develop molecular markers for breed identification .In this context, our Mahabadi goat objective was to better understand the domestication process through an extensive analysis of the mtDNA polymorphism,. More specifically, using extensive and well-controlled sampling in the field, we aimed to localize the putative domestication centers by finding the presentday wild populations bearing the closest genotypes when compared to the domestic populations [22]. All fragments of the three datasets were aligned and trimmed using Clustal W in MEGA6 Domestic goats (Capra hircus) have been selected to play an essential role in agricultural production systems, since being domesticated from their wild progenitor, bezoar (Capra aegagrus). A detailed understanding of the genetic consequences imparted by the domestication process remains a key goal of evolutionary genomics. We analyzed ten economic important native goat breeds with domestic goat ancestor.

All of the studied are phenotypically distinct from each other and have very different geographic ranges. The genetic diversity and distribution of mitochondrial haplogroups among these breeds were examined, and the level of maternal introgression of goat populations from different putative domestication centers was also assessed. Finally, to support our genetic data and initiate a detailed documentation of Capra biodiversity in Iran, the hypothesis that C. aegagrus is the wild progenitor of the Mahabadi domestic goat was evaluated. Domestic Goats are sometimes referred to as Capra aegagrus hircus, but Valdez (2011) treats the Domestic Goat as a distinct species, Capra hircus. Feral Domestic Goats have a far wider distribution around the world than do true Wild Goats. The endemic goats on Crete and nearby islands, which are often referred to as C. aegagrus cretica, look similar to wild C, aegagrus, but genetic analyses have indicated that in fact they are actually, as some researchers have suspected, feral domestic goats descended from a very early introduction (Bar-Gal et al. 2002; Masseti 2009).

Materials and Methods

We collected blood samples of native goat from Mahabadi goat. Blood samples (5ml in EDTA Containing tubes) randomly collected from 20 animals and stored at -20°C until used at biotechnology laboratory. We amplified a 598-bp fragment of the mitochondrial hyper variable region 1 (HVR1) between positions 15,653 and 16,250 in the reference goat mitochondrial genome AF533441 [24]. DNA extraction, PCR amplification and sequencing.

We collected blood samples of native goat from Mahabadi goat. Blood samples (5ml in EDTA Amplification and sequencing the complete HVR1 region was amplified by using forward primer HVR1-F: 5'-CTATCAACACACCCAAAGCTGAA-3' and reverse primer HVR1-R: 5'-CGGAGCGAGAAGAGGGAT-3'. The forward and reverse primers were designed sequences of the mtDNA genome (GenBank accession no. V00654). Polymerase chain reaction (PCR) was carried out in a total volume of 25ul, containing 10ug of genomic DNA, 2.5ul of 10ul buffer, 0.2mM of dNTP, 10pM of each primer and 1.5 units of Taq polymerase (TaKaRa, Japan). Therminal cycling was performed on a PTC-200 thermocycler (MJ Research Inc.) under the following conditions; 2 minute denaturation at 94°C, followed by 35 cycles of 30 s at 94°C, 30 s at 60°C, 60 s at 72°C, and a final 5 min at 72°C before cooling to 4°C for 10 min. The amplified products were separated by electrophoresis on 1% Agarose gels, and were visualized under UV illumination after staining with Ethidium Bromide. The PCR products were purified using QIA quick PCR purification Kit (Qiagen, USA), and were directly sequenced on an ABI 3130xl Genetic Analyzer (PE Applied Biosystems, USA) Statistical and phylogenetic analyses. The sequences of the HVR1 region from different breeds were aligned in CLUSTAL W (Thompson et al., 1994). Numbers of nucleotide polymorphic sites (S) and haplotype (h), nucleotide diversity (Pi), haplotype diversity (Hd) and nucleotide divergence (Dxy) were performed in DNA sequence polymorphism Version 5.1 [18]. The Neighbor-joining (NJ) tree [19] among haplotypes based on the HVR1 region sequences was reconstructed in MEGA 5.05 package (Tamura et al., 2011), with the reliability of the tree topology assessed by 1,000 bootstrap replications (Felsenstein, 1985). The NJ tree among breeds was constructed in MEGA 5.05 package on the basis of divergence distances.

Phylogenetic reconstruction

The sequences obtained were compared by alignment to the international Gene Bank data-base in Chinese (KM 360063), Switzerland (KR059147) , Italy (KR059205) , jordan (KR059160) , Iran (KR059191) , Spain (KR059156), Austria (KR059180) , Egypt (KR059159) , Turkey (KR059200), Cyprus (KR059163) , Saudi Arabia (KR059154), Romania(K059198), Albania (KR059146), Kyrgyzstn (KR059122), Malysia (KR059220) and Capra aegagrus (AB004076.1) using the BioEdit software program version 7.2 [20]. To investigate genetic relationship between mitochondrial sequences, an unrooted neighbor-joining phylogeny [19] was constructed using the Tamura- Nei distance method [21]. The distance computation and phylogenetic tree construction are incorporated in the MEGA package version. 5.1 (Figure 2).

Results and Discussion

(mtDNA variation in Mahabadi goat)

In the present study, we analyzed the mtDNA control region sequences of 30 Mahabadi goats to further elucidate its diversity. There were no insertions and deletions in 30 sequences of HVRI of the control regions. The HVRI sequences were highly polymorphic. Our 30 sequences gave 7 different haplotypes with 44 variable sites defined. The two largest haplotype group consisted of 6 individuals, two haplotype groups included 3 individuals, and three haplotypes included 4 individuals (Figure 5). The average base composition of the control region sequences was as follows; A: 30.38%, C: 23.77%, G: 15.70% and T: 30.16% and the molecular weight of single this sequence was 271807.00 Daltons and the molecular weight of pairs was 540684.00 Daltons and indicates that the caprine mtDNA control region has high A/T contents the control region is rich in A/C contents (Figure 1). This result indicates that Mahabadi goat The between group distances were computed using the MEGA 5.0 software .Distribution of the samples between the groups was made in accordance with the clusterization obtained. Apparently, the longest distance separated the KR059159 (Egypt) and KR059220 (Malaysia) from the others. The shortest distances were among KR059205 (Italy), Capra aegagrus (AB004076.1) and Mabadi goat. It can be reported that native goat from Iran is closed to domestic goat s ancestor (Figure 4). A sequence analysis of native goat mtDNA revealed a comparative lack of genetic structure, supporting a geographic distribution that confirms the main trends observed in previous studies of mtDNA diversity in goats. A neighbor-joining and parsimony phylogenetic tree constructed using the sequences showed that the domestic goats of Iran and Italy and Spain and the bezoar belong to the same group that this result was confirmed by trees based on the sequence of the mitochondrial displacement loop regions. Phylogenetic analysis was carried out using hyper variable region 1 (896 bp). Mahabadi goat proved to be extremely diverse (average haplotype diversity of 0.999) and the nucleotide diversity values 0.022. These results indicate highdivergence status of the Mahabadi goat and will influence breeding and conservation strategies adopted for this breed (Table 1). Distribution of the samples between the groups was made in accordance with the cluster obtained. This is possible because of geographical distance and it is distributed. The current study constitutes the first assessment of the genetic diversity and population structure of Mahabadi goat populations from the west of Iran and provides the first insights into the genetic history of native goat of Iran [23-40].