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Hybridization between yak Poephagus grunniens and taurine Bos taurus or indicine B. indicus cattle has been widely practiced throughout the yak geographical range, and gene flow is expected to have occurred between these species. To assess the impact of cattle admixture on domestic yak, we examined 1076 domestic yak from 29 populations collected in China, Bhutan, Nepal, India, Pakistan, Kyrgyzstan, Mongolia and Russia using mitochondrial DNA and 17 autosomal microsatellite loci. A cattle diagnostic marker-based analysis reveals cattle-specific mtDNA and/or autosomal microsatellite allele introgression in 127 yak individuals from 22 populations. The mean level of cattle admixture across the populations, calculated using allelic information at 17 autosomal microsatellite loci, remains relatively low (mYcattle = 2.66 ± 0.53% and Qcattle = 0.69 ± 2.58%), although it varies a lot across populations as well as among individuals within population. Although the level of cattle admixture shows a clear geographical structure, with higher levels of admixture in the Qinghai-Tibetan Plateau and Mongolian and Russian regions, and lower levels in the Himalayan and Pamir Plateau region, our results indicate that the level of cattle admixture is not significantly correlated with the altitude across geographical regions as well as within geographical region. Although yak-cattle hybridization is primarily driven to produce F1 hybrids, our results show that the subsequent gene flow between yak and cattle took place and has affected contemporary genetic make-up of domestic yak. To protect yak genetic integrity, hybridization between yak and cattle should be tightly controlled.
The yak Poephagus grunniens is a member of family Bovidae. It is endemic to the Central Asian Highlands centred round the Qinghai-Tibetan Plateau, a vast mountainous region characterized by cold and high altitude environments (typically above 3500 metres). With a current total population size of 14 million, the domestic yak constitutes one of the most important livestock genetic resources and plays an indispensable role in the life of pastoralists and agro-pastoralists in the region (Zhang 1989; Wiener et al. 2003). Today, domestic yak is distributed in Central Asia extending from the southern slopes of the Himalayas to the Altai and Hangai mountains of Mongolia and Russia, and from the Pamir Plateau and Tian-shan mountains in the west to the Qi-lian and Min-shan mountains in the east.
The hybridization of yak with cattle has been documented in ancient historical records. In China, the earliest practice of hybridization between yak and local cattle is thought to have started during the Yin Dynasty (approximately 1100 B.C.) (Cai 1989; Zhang 2000; and references therein). Such hybridization is still widely practiced today in pastoral and agro-pastoral areas across the entire geographical distribution range of the species, with observations that yak-cattle F1 hybrid animals are superior to both parental types in many aspects. For example, the F1 hybrids are reported to have better beef conformation and greater size, and to produce higher milk yields as well as to have better ability to withstand a warmer climate at lower altitudes than yak (Phillips et al. 1946a,b; White et al. 1946; Joshi 1982; Zhang 2000; Wiener et al. 2003). Traditionally, local cattle bulls are used to interbreed naturally with yak cows at higher altitudes, while reciprocal interbreeding is more common at lower altitudes. Some European cattle breeds, such as Angus, Holstein and Simmental, among others, have also been used for the exercise since the 1940s in limited areas, and this practice has been promoted through artificial insemination using frozen-thawed semen of exotic breeds since the 1970s (The Editing-Committee 1989). Whether taurine B. taurus or indicine B. indicus cattle were involved in the hybridization largely depends on the geographical area, e.g. taurine cattle were used in the Qinghai-Tibetan Plateau and Mongolian Plateau (Phillips et al. 1946a,b; Cai 1989; Zhang 1989) and indicine cattle used in the Himalayan areas and elsewhere (Phillips et al. 1946b; Joshi 1982; Wiener et al. 2003).
F1 hybrid males are sterile, while females remain fertile. Typically, after four generations of backcrossing of hybrid cows to parental bulls, hybrid males resume their fertility and the offspring are indistinguishable from ‘pure yak’ or ‘pure cattle’ in body conformation and appearance. Therefore, some animals which resemble yak probably carry genes that have been introgressed from cattle several generations earlier (Phillips et al. 1946a, b).
In yak, a mitochondrial DNA (mtDNA)-specific fragment has been described (Ward et al. 1999), and cattle autosomal microsatellite loci are now commonly used for the study of their genetic diversity (Ritz et al. 2000; Dorji et al. 2002; Xuebin et al. 2002, 2005; Qi 2004; Nguyen et al. 2005). Recently, a mtDNA study identified taurine cattle mtDNA haplotypes in two yak samples from Tibetan and Maiwa yak populations (Lai et al. 2007). However, no study has reported so far the use of genetic markers to assess the occurrence, frequency and importance of cattle introgression in individual yak or in domestic yak populations across the geographical range of the species. We report here the results of cattle admixture in domestic yak populations across the entire geographical distribution range of the species using cattle-specific mtDNA haplotypes and allelic information at 17 autosomal microsatellite loci.
A total of 1076 yak samples were collected from 29 yak populations in China, Bhutan, India, Nepal, Pakistan, Kyrgyzstan, Mongolia and Russia (Table 1 and Fig. 1a). Only phenotypically pure animals with no recent history of hybridization with cattle, as per the herder’s information, were sampled. We divided these yak populations into three major geographical groups: Qinghai-Tibetan Plateau (QTP), Himalaya and Pamir Plateau (HPP), and Mongolia and Russia (M&R), according to our previous phylogeographic analysis (Qi 2004). We further divided the QTP group into subgroups of heartland QTP and surrounding QTP according to sampling locations of yak populations either in the heartland or the surrounding areas of the Qinghai-Tibetan Plateau.
Genomic DNA was extracted following the methods described in Sambrook et al. (1989) for blood samples, Xuebin et al. (2005) for blood on Whatman FTA cards (Whatman BioScience) and Troy et al. (2001) for hair root samples. In addition, two Chinese local taurine cattle populations (Tibetan cattle, n = 26 and Wuwei cattle, n = 40) and one yak-cattle F1 hybrid population (n = 41) were also included as reference populations.
Cattle mtDNA in yak was detected through the amplification of a 357-bp taurine and indicine cattle-specific mtDNA control region fragments using primers MTD1 (5′-AGCTAACATAACACGCCCATAC-3′) and MTD2 (5′-CCTGAAGAAAGAACCAGATGC-3′) (Ward et al. 1999) in a multiplex PCR reaction also containing primers MTR1 (5′-CCCGCCTGTTTATCAAAAACAT-3′) and MTR2 (5′-CCCTCCGGTTTGAACTCAGAT-3′) (Derr et al. 1992), which amplified a 590-bp mammalian-conserved 16S rDNA fragment as an internal control. The partial mtDNA control region fragment was further sequenced for cattle-specific mtDNA detected in yak populations to verify their taurine or indicine identities. The sequences of haplotypes have been deposited in the GenBank with accession numbers AY428633–AY428639 and AY428641–AY428643. PCR amplification and sequencing were carried out as described in Appendix S1.
Seventeen unlinked bovine microsatellite loci, selected from the BovMAP database, INRA, France (http://locus.jouy.inra.fr/cgi-bin/bovmap/intro.pl) were used to genotype all the samples as described in Xuebin et al. (2005), with the annealing temperatures given in Table S1. These microsatellite loci and their allele size ranges in domestic yak are given in Table S1 and raw data are available from the corresponding author. The Nepalese yak population, consisting of hair samples only, was excluded from this analysis because of their poor amplification at the majority of microsatellite loci. Of these microsatellite loci, three loci (ILSTS013, ILSTS050 and SPS115 localized on bovine chromosomes 9, 2 and 15, respectively) yielded complete distinct allelic patterns between yak and cattle (Fig. S1), and they were therefore used as diagnostic markers for detecting cattle introgression in yak. The allele size differences at these loci between yak and cattle were further confirmed by sequencing of selected alleles.
Three methods were used to assess the impact of cattle introgression on domestic yak populations. (i) A cattle diagnostic marker-based method, using cattle mtDNA sequences and cattle-specific alleles at microsatellite loci of ILSTS013, ILSTS050 and SPS115, was used to assess the frequency of occurrence of cattle introgression in domestic yak populations at the population level. (ii) The level of cattle admixture in yak populations was assessed using an admixture estimator, mY, which is the relative contribution of two parental populations to a hybrid population and estimated using frequencies and size information of microsatellite alleles. It was initially described in Bertorelle & Excoffier (1998) and extended to any number of parental populations by Dupanloup & Bertorelle (2001). It was calculated using the program admix 2.0 (Dupanloup & Bertorelle 2001) with the two Chinese taurine cattle populations (n = 66) and the six yak populations (Pali, Kashi, Northeast Indian, East Bhutanese, West Bhutanese and Pakistani) located in the Himalaya and Pamir Plateau, showing no presence of cattle-specific mtDNA and alleles at ILSTS013, ILSTS050 and SPS115 loci (Table 1), used as parental populations for this analysis. (iii) In addition, a model-based Bayesian clustering algorithm that employs a Markov Chain Monte Carlo (MCMC) method to estimate the posterior distribution (Q) of each individual’s admixture co-efficient was used. It allows us to assess the level of cattle introgression at population as well as at individual levels. The estimator Q represents an estimate of the amount of an individual’s genome that is derived from one of the inferred parental populations (Pritchard et al. 2000). This analysis required no prior information to characterize the parental populations or to assign individuals to those populations, and was performed using allelic information at 17 autosomal microsatellite loci. It was inferred with the program structure 2.1 (Pritchard et al. 2000) with parameters K=2, a burn-in of 500 000 repetitions, and run length of 1 000 000. A Mann–Whitney U-test was applied to examine the difference of cattle introgression level among different geographical groups of yak.
A total of 19 cattle mtDNA sequences (1.8%) were detected in 1076 yak. More particularly, cattle mtDNA was detected in 11 out of the 29 yak populations with a within-population frequency ranging from 2.1% (n = 1, Tianzhu White) to 10.9% (n = 5, Tianzhu Black). Of the 19 yak carrying cattle mtDNA, 11 were males and eight females. These cattle mtDNA sequences were predominantly observed in the QTP (n = 14 or 3.16% of the animals) and M&R (n = 4 or 1.75% of the animals) groups, and only sparsely in the HPP group (n = 1 or 0.25% of the animals). The QTP group had a significantly higher frequency of cattle mtDNA sequences than the HPP group (P<0.05), however, the frequency was not statistically different between the QTP and M&R (P=0.10) groups and between the M&R and HPP (P=0.35) groups. The frequency of yak with cattle mtDNA sequences in the surrounding QTP subgroup (6.18%) was significantly higher than that in the heartland QTP subgroup (1.13%) (P<0.05) (Table 1).
To further verify the taurine or indicine origin of cattle mtDNA introgression in yak, a partial mtDNA control region sequence (486 bp) was obtained for 17 out of the 19 cattle mtDNA genomes detected in the yak populations. We failed to obtain mtDNA sequences for two samples from the Chinese Maiwa yak population. Comparison of the 17 cattle mtDNA sequences detected in yak populations with published cattle sequences (Troy et al. 2001) indicated their taurine cattle origin for all. The phylogenetic analysis further assigned these sequences into 10 haplotypes defined by polymorphisms at 11 sites. One haplotype (AY428637) occurred seven times (four in Tianzhu Black, two in Datong and one in Gobi Altai population), another one (AY428636) occurred twice (one in Tianzhu Black and one in Central Bhutanese population), and the remaining eight haplotypes only occurred once. According to the haplotype definitions described in Troy et al. (2001), these 10 haplotypes belong to the T3 haplogroup, which predominates in European cattle (Troy et al. 2001). Similarly, the T3 haplogroup also predominates in Chinese taurine cattle (Lai et al. 2006), and therefore it is not possible to determine whether these haplotypes detected in yak populations were introgressed from either European or Chinese local taurine cattle.
As illustrated in Fig. S1, the allelic genotype patterns overlapped between yak and cattle in 14 out of the 17 microsatellite loci genotyped, therefore it was not possible to determine the cattle-specific alleles at these loci. However, three microsatellite loci (ILSTS013, ILSTS050 and SPS115) yielded allele sizes that were completely distinct between yak and cattle (Appendix S1). These alleles have been further sequenced to confirm their size differences between yak and cattle (Feng et al. 2009).
A total of 26 yak-specific and 29 cattle-specific alleles were amplified at ILSTS013, ILSTS050 and SPS115 loci in yak, cattle and yak-cattle F1 hybrid populations. Of the 29 cattle-specific alleles, 16 were detected in 22 out of the 28 yak populations (the Nepalese yak population was excluded from admixture analyses because of their poor amplification at the majority of microsatellite loci). The frequency of these cattle-specific alleles in yak populations varies widely among loci (Table 1). More precisely, six cattle-specific alleles were detected at ILSTS013 in 38 yak individuals from 16 populations, and the frequency of yak carrying cattle alleles varied from 2.0% (n = 1, Chinese Jiali) to 29.2% (n = 7, Chinese Jiulong). It was not statistically different among the QTP, HPP and M&R groups (P>0.05). At ILSTS050, five cattle-specific alleles were detected in a total of 12 yak individuals from seven populations with frequencies ranging from 2.2% to 6.3% and similar among the QTP, HPP and M&R groups (P>0.05). Five cattle-specific alleles at SPS115 were detected in 64 yak individuals from 17 populations. The frequency was significantly higher in the QTP (13.32%) than in the HPP (0.79%) and M&R (0.88%) groups (P<0.001) while there was no difference between the HPP and M&R groups (P>0.05). As observed in introgressed cattle mtDNA sequences, this cattle-specific autosomal microsatellite allele-based method detected cattle introgression events predominantly in the QTP and M&R yak groups. However, unlike the mtDNA results, the frequency of cattle introgression detected in the heartland QTP and surrounding QTP subgroups was similar (P>0.05) at each of the three microsatellite loci. When the data at three microsatellite loci were combined together, the frequency of cattle introgression was significantly higher in the QTP group (18.74%) than in the HPP (3.46%) and M&R (5.70%) groups (P<0.01), while no difference was detected between the HPP and M&R groups (P=0.09), and between the heartland QTP (16.98%) and surrounding QTP (21.35%) subgroups (P=0.33).
We combined the data from mtDNA and three diagnostic microsatellite loci (ILSTS013, ILSTS050 and SPS115) to calculate the frequency of yak carrying cattle genes introgressed from mitochondrial and/or nuclear genome in each population. A total of 127 or 11.80% yak from 22 populations were found to have introgressed cattle mtDNA sequences and/or autosomal microsatellite alleles (Table 1). Some yak individuals showing cattle mtDNA sequences do present a typical yak microsatellite profile (Table S2). The distribution of the frequency of cattle-specific mtDNA sequences and microsatellite alleles is shown in Fig. 1b. The frequency at the population level ranged from 2.3% (Kyrgyzstan yak) to 41.7% (Chinese Maiwa yak). Cattle-specific sequences/alleles were absent in six HPP yak populations (Pali, Kashi, Northeast Indian, East Bhutanese, West Bhutanese and Pakistani yak). This combined analysis indicated a significantly higher frequency of cattle introgression in the QTP group (21.44%) than in the M&R (7.46%) and HPP groups (3.70%) (P<0.01). This frequency was also significantly higher in the surrounding QTP (26.97%) subgroup than in the heartland QTP (17.78%) subgroup (P<0.05). The M&R group also showed a relatively higher frequency of cattle introgression than the HPP group (P=0.084). Cattle introgression was found in four out of the 10 yak populations in the HPP areas (Northwest Indian, Central Bhutanese, Aksu and Kyrgyzstan) with frequencies ranging from 2.27% to 18.18% (Table 1).
To assess the level of cattle introgression in domestic yak populations at genome level, we determined the mean cattle admixture proportion in domestic yak populations using admixture analyses based on both allele frequency and allele size information (mY), and a model-based Bayesian clustering algorithm. We obtained negative estimates of mY in five yak populations of Pali, Kashi, Aksu, West Bhutanese and Kyrgyzstan as well as in the HPP group, and these negative mY values were set to zero. The mY analysis detected an average proportion of 2.66 ± 0.53% cattle genetic admixture in domestic yak populations, with values ranging from zero (Pali, Kashi, Aksu, West Bhutanese and Kyrgyzstan) to 7.36% (North Hangai). Similar levels of mean cattle admixture proportions were detected in the QTP (3.90 ± 0.62%) and M&R (4.78 ± 0.75%) groups (P=0.45), and they were significantly higher than that in the HPP group (0.00 ± 0.58%, P<0.01) (Table 2, Fig. 1c). There was no difference in the level of cattle admixture between the heartland QTP and surrounding QTP subgroups (P>0.05). Fig. 2 shows the variation of the mean cattle admixture proportion in terms of mY among the 28 yak populations and geographical groups. As compared with the diagnostic marker-based method and excluding the populations with negative values of mY, admixture analysis also detected cattle introgression in Northeast Indian, East Bhutanese and Pakistani yak populations, in which no cattle-specific mtDNA sequence or autosomal microsatellite alleles at ILSTS013, ILSTS050 and SPS115 were detected.
By applying a model-based Bayesian clustering algorithm using allelic information at 17 autosomal microsatellite loci, we inferred an average proportion of 0.69 ± 2.58% cattle admixture co-efficient (Qcattle) in the yak genome, with values ranging from 0.15 (East Bhutanese) to 2.68 (North Hangai). The Qcattle was 0.73 ± 1.97% in the QTP group, which was relatively lower than that in the M&R group (1.29 ± 4.62%) (P=0.92) but significantly higher than that in the HPP group (0.32 ± 0.92%) (P<0.01). The Qcattle was only higher in the M&R group than in the HPP group at a marginally significant level (P=0.065). Similar to the mY analysis, the Qcattle was not statistically different between the heartland QTP (0.77 ± 2.06%) and surrounding QTP (0.67 ± 1.85%) subgroups (P=0.46) (Table 2). Fig. 2 shows the variation of the inferred Qcattle among 28 yak populations and geographical groups. This model-based Bayesian clustering method also showed that the mean level of cattle admixture was much higher in the QTP and M&R groups than that in the HPP group (Fig. 1d).
At an individual animal level, the inferred Qcattle was only 0.1–0.3% in 861 yak (81.92%), likely corresponding to background levels (Kaeuffer et al. 2007). It, however, reached a value of 32.9% in an individual of the North Hangai population. A total of 14 yak individuals showed values ranging from 12.5% to 32.9% of inferred cattle admixture, and 91 individuals had values ranging from 1.00% to 9.80% of inferred cattle admixture.
Yak-cattle hybrid F1 animals are most popular in agro-pastoral areas at altitudes ranging from 1500 to 2500 metres (Zhang 1989), and therefore a hybridization zone might be expected at and around these altitudes. Although admixture estimates of mY and Qcattle showed a clear geographical structure, with higher levels of admixture in the QTP and M&R regions and lower levels in the HPP region (Fig. 1c and d), our results indicated that there was no significant correlation (P>0.05) between the level of cattle admixture in terms of mtDNA or microsatellite diagnostic markers, mY or Qcattle estimates and the altitude across geographical regions (Fig. S2) and within geographical region (Fig. S3).
Ancient nomadic people are believed to have started hybridization of yak with cattle 3000 years ago (Cai 1989; Zhang 1989, 2000). Cattle bulls are commonly used to hybridize with yak cows at relatively high altitudes, while reciprocal crossing is practiced at low altitudes of their distribution range (e.g. Phillips et al. 1946a,b; Cai 1980; Joshi 1982; Zhang 1989; Adachi & Kawamoto 1992; Davaa 1996; Tshering et al. 1996). Hybrid males are sterile and their fertility does not resume until the fourth backcrossing generation (Deakin et al. 1935; Cai 1989; Tumennasan et al. 1997; Zhang 2000; Hisabumi et al. 2002), and therefore male-mediated cattle introgression in yak is impossible (e.g. Jianlin et al. 2002) and thus the cattle genes are only introduced into yak genome by hybridization of female F1 hybrids to yak. Consequently, Y-chromosome–specific markers are not helpful in detecting cattle introgression in domestic yak.
In this study, we first chose a cattle-specific mtDNA control region fragment (Ward et al. 1999) and cattle-specific alleles at three autosomal microsatellite loci (ILSTS013, ILSTS050 and SPS115) for a diagnostic approach to assess the impact of cattle introgression on domestic yak populations. We also chose an estimator of admixture proportion and a model-based Bayesian admixture analysis, two methods that have been widely used for estimating the admixture proportion between closely related species (Hanotte et al. 2002; Freeman et al. 2004; Edwards et al. 2007), in order to estimate cattle admixture proportion in the yak genetic pool at the genome level. The mY estimator was chosen as it appears suitable for estimating admixture proportion using molecular data. The mY has also the advantages of no bias and relatively low variance, in comparison to two other conventional estimators of mR (Roberts & Hiorns 1965) and mC (Chakraborty et al. 1992), which only consider gene frequencies. Bayesian admixture analysis requires no prior information on the identity of possible parental populations or on the possible assignment of individuals into populations. It was performed using allelic information at 17 microsatellite loci.
The diagnostic marker-based approach detected cattle introgression in 22 out of 29 yak populations with an average frequency of 11.8%, and 127 individuals showed cattle-specific mtDNA sequences and/or autosomal microsatellite alleles. The QTP group had a significantly higher frequency of cattle introgression than the M&R group, followed by the HPP group (P < 0.01). The frequency of cattle introgression in the surrounding QTP subgroup was significantly higher than that in the heartland QTP subgroup (P < 0.05). Although the diagnostic marker approach identified a relatively high incidence of cattle introgression in contemporary domestic yak populations, it does not allow us to estimate the level of cattle introgression into the yak genome. We therefore applied two admixture analyses using allelic information at 17 microsatellite loci dispersed throughout the genome. Both mY admixture and Bayesian admixture estimations indicated that the average proportion of cattle admixture in the contemporary domestic yak genome was generally low at a population level. However, it varied a lot among the populations and geographical groups, and also among individuals within a population.
Out of the 17 yak detected with taurine mtDNA sequences, only two also had a cattle allele at one of the three diagnostic microsatellites loci and only three showed a Qcattle above 0.3% (Table S2). It is therefore important to combine information from genetic markers with different modes of inheritances as well as to perform data analyses using different statistical approaches in order to assess introgression between yak and cattle. Interestingly, while the large variation of cattle admixture across individuals within population suggests an ongoing process of cattle introgression under the assumption that genetic imprints of ancient cattle introgression would be ‘homogenized’ at the yak genome level, the detection of yak individuals with only cattle mtDNA sequences is also an indication of ancient introgression events.
Yak pastoralism is a transhumant and seasonal activity, and yak herders usually keep yak-cattle F1 hybrid and backcross animals as packing, riding or draught animals (Wiener et al. 2003). Traditionally, hybridization between yak and cattle and backcrossing of F1 hybrid females are driven to produce the F1 and first generation (B1) of backcross hybrids only (Zhang 1989, 2000; Wiener et al. 2003), and therefore a high frequency of cattle introgression in domestic yak populations is not expected. We observed, however, a high incidence of cattle introgression in contemporary domestic yak populations, typically in the QTP and M&R groups where F1 and first generation of backcross (B1) hybridization have been practiced for thousands of years (Zhang 1989, 2000; Davaa 1996; Wiener et al. 2003). This suggests that these practices had and still have an impact on the yak genetic integrity. Unattended management of free-ranging animals, especially during the breeding seasons in summer pastures, may account for the high frequency of cattle introgression in yak populations (Phillips et al. 1946a,b; Wiener et al. 2003).
In addition, other factors such as the geographical locations where yak pastoralism is practiced, founder effect and breeding strategy may explain the variations of frequency of cattle introgression among yak populations within and among geographical areas. For example, yak-cattle hybridization is not common in the pastoral areas at high elevations where cattle cannot adapt well, while it is widespread in areas of agro-pastoral zone at relatively low altitudes (Wiener et al. 2003). This is consistent with our observations that the surrounding QTP subgroup displayed a significantly higher frequency of cattle introgression than the heartland QTP subgroup. In particular, the highest frequency of cattle introgression was detected in the Jiulong (37.50%) and Maiwa (41.67%) populations, which are located in the surrounding QTP areas. In the case of the Maiwa yak, hybridization between yak and taurine cattle has been widely carried out to improve its milk production (Cai 1980, 1989), while Jiulong yak are the descendants of a small population that survived a severe outbreak of rinderpest 150 years ago (Wiener et al. 2003). A contemporary population of 50 000 yak was developed from a small population of survivors, and hybridization between yak and local cattle may have occurred in the process of population recovery and expansion, with a closed breeding programme being responsible for the high frequency of individuals carrying cattle-specific mtDNA sequences and/or autosomal microsatellite alleles in the population.
A generally low frequency of cattle introgression was observed in the HPP group distributed at relatively high elevations (approximately 3500 metres), where yak-cattle hybrids seem to be unattractive to the pastoralists because of their poor adaptability to this habitat (Pal & Madan 1996; Rasool et al. 2002). This confirms the claim that hybridization is rare in the majority of HPP yak populations except for the Indian, Bhutanese and Nepalese Himalayan areas where hybridization between yak and taurine or indicine cattle has been reported (Joshi 1982; Pal & Madan 1996; Sherchand & Karki 1996; Dorji et al. 2002; Wiener et al. 2003).
Although hybridization is supposedly being practiced with local cattle populations in wide yak-rearing areas, the European taurine cattle have also been used for the exercise since 1940s (Wiener et al. 2003). Our mtDNA-based approach indicated that all cattle mtDNA sequences detected in yak populations were of T3 taurine cattle (Troy et al. 2001), which are equally predominant in both European and Chinese cattle populations, and therefore the respective impact of European or local cattle introgression on domestic yak populations cannot be assessed. Also, it should be noted that while we failed to sequence the mtDNA of two Maiwa yaks showing a diagnostic cattle fragment, the absence of any indicine cattle within or around the current distribution of Maiwa yak does make it unlikely that there is any zebu cattle introgression in this population. Our study clearly illustrates the impact of taurine cattle introgression into domestic yak, although it does not provide any evidence of zebu introgression into yak populations. It is well-known that yak-cattle hybridization is primarily driven to produce F1 and B1 hybrids, and our results indicate the presence of gene flow between yak and cattle in the majority of contemporary yak populations. Our findings suggest that cattle introgression is an ongoing process and might have been relatively more important in recent times. To protect yak genetic integrity, the hybridization between yak and cattle should therefore be tightly controlled.
We are grateful to Tao SX, Hu J, Liang YL, Ni Z, Tashi T, Zheng YC, Zhong GH, Mao XL, Liu CL, Ni YA, Lu ZL, (China), Lkhagva B, Badamdorj D (Mongolia), Dorji T (Bhutan), Sherchand L (Nepal), Phuntsog T, Ali M (India), Afzal M, Naqvi AN (Pakistan), Kachkynbaeva K, Cholponkulov T (Kyrgyzstan), and Chekarova I (Russia) for providing samples or assistance in the process of sampling. We thank Dr Miika Tapio and two anonymous reviewers for their critical comments of the manuscript. This study is principally funded by ILRI programme grants from the United Kingdom, Japan, The European Union, Ireland and France, and unrestricted funding from other donors to the CGIAR, and the 973 program of China (2007CB815704), National Natural Science Foundation of China (NSFC) (30771181, 30870295), the West Light Doctoral Program of the Chinese Academy of Sciences, and the Natural Science Foundation of Yunnan province of China (2007C100M). This is ILRI publication IL-200904.
Additional supporting information may be found in the online version of this article.
Figure S1 Allele spectra of 17 microsatellite loci in yak, cattle and their F1 hybrid populations. The Y-axis represents the allele frequency and the X-axis the allele sizes.
Figure S2 Correlation between the level of cattle admixture and the altitude of geographic location across geographic regions.
Figure S3 Correlation between the level of cattle admixture and the altitude of geographic location within geographic region.
Table S1 Seventeen microsatellite loci and their PCR conditions and allele size ranges in domestic yak populations.
Table S2 Yak individuals showing cattle-specific mtDNA and microsatellite alleles and Qcattle proportions.
Appendix S1 Supplementary methods and results.
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