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Discrimination of Korean cattle (Hanwoo) using DNA markers derived from SNPs in bovine mitochondrial and SRY genes.

ABSTRACT : In order to distinguish Korean cattle (Hanwoo) beef from the imported beef from Australia in Korean markets, DNA markers based on PCR-RFLP from mitochondrial genes and SRY gene were applied. A total of 2,826 beef samples comprising 1,495 Hanwoo and 1,331 foreign cattle breeds were obtained in Korea. An 801 bp fragment of the SRY gene on the bovine Y chromosome, a 343 bp fragment of ND4 gene and a 528 bp fragment of ND5 gene in the bovine mtDNA were amplified by PCR and digested with three restriction enzymes, MseI, HpyC[H.sub.4]III and Tsp509I, respectively. The results showed that Bos taurus (T) type was the majority in Hanwoo by combining three markers (99.5%). However, 78.2% of Bos indicus (I) type was observed in the imported beef samples. These results indicated that three markers used in this study will be used as valuable markers for discriminating imported beef against Hanwoo. (Key Words : Hanwoo, Bos taurus, Bos indicus, PCR-RFLP, SRY, ND4, ND5)

INTRODUCTION

Korean cattle, also called Hanwoo, is a well-known domestic cattle breed in Korea and the recorded population of this breed was about 1.84 million heads in 2006 (Statistics in the Ministry of Agriculture and Forestry in Korea, 2006). Because of their high meat quality and the breed reputation, Korean consumers are eager to buy Hanwoo meat rather than imported beefs, even though the price of Hanwoo meat is higher.

Since 1990, large amount of beef was imported from outside of Korea and their market share in 2005 was about 70% of the beef consumed in Korea. Because of the high price of the Hanwoo beef compared with the imported beef, some of the mislabeled beef has arisen, resulting illegal false sales. Also because of the outbreak of Bovine spongiform encephalopathy (BSE) in the United States in 2003, consumers prefer to know the exact origin of the beef that they have. In this point of view, the Korean Ministry of Agriculture and Forestry is planning to launch traceability system for the Hanwoo beef in order to trace beef from farm to table. However, settlement of this system takes couple of years from now and discrimination of Hanwoo beef from other imported beef is urgently needed in order to satisfy consumers and protect false sales of the beef.

Until recently, only 33 DNA markers have been developed using the causative mutations for disease or production traits in cattle (http://omia.angis.org.au/) and the number of markers will be rapidly growing. In Korea, a breed discrimination marker based on the coat color related MC1R (melanocortin 1 receptor) gene between Hanwoo and Holstein was developed (Kim et al., 2000; Lee et al., 2000) and the impact of this marker to the society is enormous in relation to give trust to the consumers and decrease the mislabeled false sales. In China, two domestic Buffalo populations were differentiated with the SNPs in Y-linked SRY gene and microsatellite markers were also used for population genetic studies (Hai-Guo et al., 2005; Zhang et al., 2006). Very recently, Sasazaki et al. (2006) developed AFLP (Amplified Fragment Length Polymorphism) oriented DNA markers in order to discriminate between Japanese Black cattle and F1 (Japanese Black cattle x Holstein) breeds. They showed that the probability of identifying F1 was 0.9168 and the probability of misjudgment was 0.0066 using only four selected markers. Subsequently, in order to distinguish between Japanese domestic and Australian imported beef in Japan, Sasazaki et al. (2007) developed DNA markers derived from mtDNA, SRY gene, MC1R gene and AFLP.

The aim of this study was to develop DNA markers for discrimination of Hanwoo beef compared with the imported beef. Since the outbreak of BSE in USA in 2003, most of the imported beef came from Australia and large number of cattle was crossbred with Bos indicus breeds in order to overcome hot and arid environments in Australia. Take this point account, previously reported DNA mutations for Bos indicus breeds in two mitochondrial genes (ND4 and ND5) and SRY gene (Sasazaki et al., 2007) were investigated as possible DNA markers for discrimination between Hanwoo and imported cattle breeds in Korea.

MATERIALS AND METHODS

Genomic DNA preparations

Genomic DNA samples were extracted from blood or meat samples in three Universities (Gyeongsang National Univ., Chungbuk National Univ. and Konkook Univ.) and National Institute of Animal Science (NIAS) in Korea using commercially available several DNA extraction kits. Total 2,826 DNA samples, composed of 1,495 samples from Hanwoo (Korean cattle) and 1,331 DNA samples from imported cattle, mainly from Australia, were investigated.

Designing of primers

Primers for PCR amplification of the SRY, ND4 and ND5 genes were designed basically according to Sasazaki et al. (2007). In case of SRY gene, Bos taurus SRY gene sequence (AB039748) was aligned with that of Bos indicus sequence (AY079145) and identified the nucleotide mismatches, which were used for the breed differentiation marker based on the PCR-RFLP using MseI restriction enzyme. Therefore, the PCR primers were designed to span this mutation and the size of PCR products was decided for giving optimum results obtained from PCR-RFLP. Similarly, nucleotide mutations between Bos taurus and Bos indicus sequences in ND4 and ND5 genes were also investigated. Primers were designed to amplify a 343 bp PCR fragment corresponding to nucleotides 10,960-11,302 in ND4 gene and a 528 bp PCR fragment corresponding to nucleotides 12,507-13,034 in ND5 gene from the Bos taurus mtDNA sequence (GenBank accession number V00654) (Anderson et al., 1982). Nucleotides 10,963-12,305 in ND4 gene and nucleotides 12,510-13,037 in ND5 gene from the Bos indicus mtDNA sequence (GenBank accession number NC_005971) were also amplified using these primers. The adenine in nucleotide position at 11,071 of ND4 gene in Bos indicus mitochondrial sequence was not recognized by the restriction enzyme HpyC[H.sub.4]III and showed the different PCR-RFLP patterns between Bos taurus and Bos indicus breeds. Also, the thymine in nucleotide position at 12,923 of ND5 gene in Bos taurus mitochondrial sequence was not recognized by the restriction enzyme Tsp509I. The primer information for SRY, ND4 and ND5 genes was shown in Table 1.

Polymerase chain reaction

The Polymerase Chain Reaction (PCR) was conducted in 25 [micro]l volumes, each containing 10 x PCR Gold buffer, 1.5 mM Mg[Cl.sub.2], 200 [micro]M of each dNTP, 10 pmol of each primer, 1 unit of Taq DNA polymerase (Ampli Taq Gold, USA) and 50 ng of template DNA. The PCR amplification reaction was carried out using a GeneAmp[R] PCR System 2700 (Applied Biosystems, USA). The PCR conditions for the three genes investigated are represented in Table 2.

[FIGURE 1 OMITTED]

Restriction enzyme digestion and gel electrophoresis

Three restriction enzymes, namely MseI, HpyC[H.sub.4]III, Tsp509I (New England Biolabs, USA), were used for PCR-RFLP tests in SRY, ND4 and ND5 genes, respectively. The PCR products were digested in a total volume of 20 [micro]l including 15 [micro]l of the PCR products, 2 [micro]l of 10x reaction buffer, 5 units each of restriction enzymes and the reaction was carried out overnight at 37[degrees]C for MseI and HpyC[H.sub.4]III and at 65[degrees]C for Tsp509I restriction enzymes. The digested products were electrophoresed in 3% (SRY, ND5) or 5% (ND4) agarose gels and visualized on the UV light for identifying different restriction enzyme digestion patterns between Bos taurus (Hanwoo) and Bos indicus alleles.

RESULTS AND DISCUSSION

The partial fragments of SRY, ND4, ND5 genes were successfully amplified by PCR and the product sizes were 801 bp, 343 bp and 528 bp, respectively, as expected. These PCR fragments were subjected to three restriction enzyme digestions in order to identify Bos indicus and Bos taurus alleles, which were used for breed differentiation between imported and Hanwoo beefs. Specifically, MseI was used for SRY gene and two mitochondrial gene fragments, ND4 and ND5, were digested by HpyC[H.sub.4]III and Tsp509I restriction enzymes, respectively. The PCR-RFLP patterns in Bos taurus and Bos indicus breeds were shown in Figure 1. For the ND4 restriction enzyme digestion fragments, one (29 bp) of the four fragments (185, 79, 50 and 29 bp) was not shown in Bos taurus because of the low resolution of the pictures for the small fragments on the agarose gel.

The identified Bos indicus and Bos taurus specific alleles were investigated whether they can use for the discrimination of DNA markers between Hanwoo and imported beef samples in Korea. The PCR-RFLP results from 1,495 Hanwoo meat samples showed that 1,445 (96.7%) Hanwoo samples had Bos taurus alleles, indicating the high possibility for using this SRY marker as breed discrimination. However, the SRY gene is located only in Y chromosome and because of this, the SRY marker can not be used for beef samples from cows. In Table 3, 50 beef samples (3.3%) are females. The PCR-RFLP results for the SRY gene in imported beef samples from Australia indicated that 58.2% of the samples had Bos indicus alleles. This result suggested that large number of Australian cattle was mixed with Bos indicus cattle breeds, mainly Brahman, in order to overcome arid environmental conditions. In imported beef samples, the PCR amplification was not succeed for 214 samples (16.1%). Most of these are assumed to be the female samples, but unfortunately we do not have any gender information for the imported beef samples. The results of the SRY marker indicated that this marker is very powerful for discrimination of the imported beef samples. However, there is a limitation for using this marker for breed discrimination in female beef samples.

In order to identify female origin of the beef samples, two mitochondrial genes, ND4 and ND5, were investigated. Both markers were almost same results for Bos taurus and Bos indicus allele frequencies. In imported beef samples, the observed Bos indicus allele frequencies were very similar that 44.6% of Bos indicus allele frequency was observed in ND4 gene and 43% was observed in ND5 gene. This is not surprising that these two genes have similar gene frequencies because these two genes located on the mitochondrial genome with no homologous recombination and will be inherited in a maternal lineage. However, small portion of the samples were identified as neither Bos taurus nor Bos indicus alleles. They are actually mixed type of the alleles due to the heteroplasmy of the mitochondrial genome. Therefore more investigation should be carried out for the mixed type of the beef samples that they are really came from the heteroplasmy of the mitochondrial genome, not from the experimental errors. When these two mitochondrial genes applied to Hanwoo beef samples, 1,487 beef samples (99.5%) showed Bos taurus allele, indicating our assumption was true that the Hanwoo is Bos taurus breed. However, we also observed small portion of Bos indicus allele frequency (0.5%) in Hanwoo population. These results may support the hypothesis that Hanwoo breed had not been originated from a crossbred between Bos primigenius in Europe and Bos indicus in India, however, North Eastern Asian cattle breeds might be had separate domestication from the European and African Bos taurus followed by the small extents of Bos indicus influx (Mannen et al., 2004; Yoon et al., 2005).

Using the three markers together, the discrimination rate from imported beef samples was calculated. If the animal has at least one Bos indicus allele, this can be specified as Bos indicus origin and decided that this animal is different from Hanwoo. Using this process, the observed frequencies of Bos indicus origin were 78.21% and 0.54% for imported and Hanwoo beef samples, respectively. The huge differences of these allele frequencies indicate that these markers will be used as breed differentiation, especially imported beef from Australia against Hanwoo samples. In order to achieve 100% discrimination for breed identification, autosomal DNA markers are ultimately needed in the future. The current progress of molecular biology and recent success of bovine genome sequencing will make this possible in a short period of time.

ACKNOWLEDGEMENTS

This work was supported by a grant from Biogreen21 program (code # 20070501034006), Rural Development Administration, Republic of Korea and by a grant No R11-2002-100-01008-0 of the ERC program of the Korean Science & Engineering Foundation.

Received April 11, 2007; Accepted July 22, 2007

REFERENCES

Anderson, S., M. H. L. de Bruijn, A. R. Coulson, I. C. Eperon, F. Sanger and I. G. Young. 1982. Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome. J. Mol. Biol. 156(4):683-717.

Hai-Guo, J., Z. Yu-min and Z. Gou-li. 2005. Analysis of microsatellite DNA polymorphisms in five china native cattle breeds and application to population genetic studies. Asian-Aust. J. Anim. Sci. 18(12):1696-1700.

Kim, T. H., D. H. Yoon, E. W. Park, H. Y. Lee, S. J. Oh, I. C. Cheong, T. Y. Thak, K. N. Kim and J. Y. Han. 2000. A study on genotyping frequencies of the bovine melanocortin receptor 1 (MC1R) in cattle breeds. Kor. J. Anim. Sci. Technol. 42(6):735-744.

Lee, S. S., Y. H. Yang, S. Y. Kang, W. Y. Oh, B. S. Yang, S. B. Ko, S. J. Oh and K. I. Kim. 2000. Comparison of the genotypes and frequencies of MSH receptor (MC1R) gene in Korean cattle, Cheju native black cattle, Japanese black and Japanese brown cattle. Kor. J. Anim. Sci. Technol. 42(3):253-260.

Mannen, H., M. Kohno, Y. Nagata, S. Tsuji, D.G. Bradley, J. S. Yeo, D. Nyamsamba, Y. Zagdsuren, M. Yokohama, K. Nomura and T. Amano. 2004. Independent mitochondrial origin and historical genetic differentiation in North Eastern Asian cattle. Mol. Phylogenet. Evol. 32:539-544.

Sasazaki, S., T. Imada, H. Mutoh, K. Yoshizawa and H. Mannen. 2006. Breed discrimination using DNA markers derived from AFLP in Japanese beef cattle. Asian-Aust. J. Anim. Sci. 19(8):1106-1110.

Sasazaki, S., H. Mutoh, K. Tsurifune and H. Mannen. 2007. Development of DNA markers for discrimination between domestic and imported beef. Meat Sci. 77(2):161-166.

Yoon, D., E. W. Park, S. H. Lee, H. K. Lee, S. J. Oh, I. C. Cheong and K. C. Hong. 2005. Assessment of genetic diversity and relationships between Korean cattle and other cattle breeds by microsatellite loci. Kor. J. Anim. Sci. Technol. 47(3):341-354.

Zhang, Y., D. Sun, Y. Yu and Y. Zhang. 2006. A Y-linked SNP in SRY gene differentiates Chinese indigenous swamp buffalo and introduced river buffalo. Asian-Aust. J. Anim. Sci. 19(9): 1240-1244.

D. Yoon (1), Y. S. Kwon (2), K. Y. Lee (2), W. Y. Jung (2), S. Sasazaki (3), H. Mannen (3), J. T. Jeon (4) and J. H. Lee (2), *

(1) Division of Animal Genomics and Bioinformatics, National Institute of Animal Science, Suwon, 441-350, Korea

(2) Division of Animal Science and Resources, Research Center for Transgenic Cloned Pigs, Chungnam National University, Daejeon, 305-764, Korea.

(3) Graduate School of Agricultural Science, Kobe University, Kobe, 657-8501, Japan.

(4) Division of Applied Life Science, Gyeongsang National University, 900 Gaiwa-dong, Jinju, Gyeongnam, 660-701, Korea.

* Corresponding Author: J. H. Lee. Tel: +82-42-821-5779, Fax: +82-42-825-9754, E-mail: junheon@cnu.ac.kr
Table 1. Primer information for amplifying SRY, ND4 and
ND5 genes and restriction enzymes used to distinguish
Bos taurus and Bos indicus alleles

Genes PCR product sizes Primer sequence

SRY 801 bp F 5' -TTAGAACGCTTACACCGCATATTACTTC-3'
 R 5' -TAGTAAAATTGAGATAAAGAGCGCCTTTGTTAG-3'
ND4 343 bp F 5' -CGCCGGACTCTATTTCCTATTCT-3'
 R 5' -TGCTATAAAGTCGGTCATAGGGT-3'
ND5 528 bp F 5' -CGCAAACAACCTCTTCCAGCTATTC-3'
 R 5' -TGACTGGATGTGGAGAAGGCGATGA-3'

Genes Restriction enzymes used

SRY MseI

ND4 HpyC[H.sub.4]III

ND5 Tsp509I

Table 2. The PCR conditions for amplifying SRY, ND4
and ND5 genes

 SRY

Initial incubation step
Denaturation 94[degree]C 30 sec 38 cycles
Annealing 60[degree]C 30 sec
Extension 72[degree]C 45 sec
Final extension
Final step

 ND4

Initial incubation step 94[degree]C 10 min (1 cycle)
Denaturation 94[degree]C 30 sec 35 cycles
Annealing 65[degree]C 30 sec
Extension 72[degree]C 30 sec
Final extension 72[degree]C 10 min (1 cycle)
Final step 4[degree]C [infinity]

 ND5

Initial incubation step
Denaturation 94[degree]C 30 sec 35 cycles
Annealing 63[degree]C 30 sec
Extension 72[degree]C 35 sec
Final extension
Final step

Table 3. The number of animals showing Bos taurus (T)
and Bos indicus (I) alleles in SRY, ND4 and ND5 genes
in imported beef and Hanwoo samples

Gene Type Imported beef Hanwoo beef

SRY (%) T 342 (25.7) 1,445 (96.7)
 I 775 (58.2) 0 (0.0)
 NA 214 (16.1) (1) 50 (3.3) (2)
ND4 (%) T 671 (50.4) 1,487 (99.5)
 I 594 (44.6) 8 (0.5)
 NA 66 (5.0)3 0 (0.0)
ND5 (%) T 661 (49.7) 1,487 (99.5)
 I 573 (43.0) 8 (0.5)
 NA 97 (7.3) (4) 0 (0.0)
Occurrence of Bos
 indicus alleles (%) 1,041/1,331 8/1,495
 (78.21) (0.54)

(1) Unable to amplify PCR products.

(2) Indicates female beef samples.

(3) 58 were not amplified by PCR and 8 were identified
as mixture type.

(4) 91 were not amplified by PCR and 6 were identified
as mixture type.
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Article Details
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Title Annotation:single nucleotide polymorphisms, Sex-determining Region Y
Author:Yoon, D.; Kwon, Y.S.; Lee, K.Y.; Jung, W.Y.; Sasazaki, S.; Mannen, H.; Jeon, J.T.; Lee, J.H.
Publication:Asian - Australasian Journal of Animal Sciences
Article Type:Report
Geographic Code:9SOUT
Date:Jan 1, 2008
Words:2875
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