• 한국동물번식학회:학술대회논문집
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• 한국동물번식학회 2001년도 발생공학 국제심포지움 및 학술대회 발표자료집
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• pp.37-43
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• 2001

1. About fifty thousand of cattle embryos were transferred and 16000 ET-calves were born in 1999. Eighty percents of embryos were collected from Japanese Black beef donors and transferred to dairy Holstein heifers and cows. Since 1985, we have achieved in bovine in vitro fertilization using immature oocytes Collected from ovaries of slaughterhouse. Now over 8000 embryos fertilized by Japanese Black bull, as Kitaguni 7 -8 or Mitsufuku, famousbulls as high marbling score of progeny tests were sold to dairy farmers and transferred to their dairy cattle every year. 2. Embryo splitting for identical twins is demonstrated an useful tool to supply a bull for semen collection and a steer for beef performance test. According to the data of Dr.Hashiyada (2001), 296 pairs of split-half-embryos were transferred to recipients and 98 gave births of 112 calves (23 pairs of identical twins and 66 singletons). 3. A blastomere-nuclear-transferred cloned calf was born in 1990 by a joint research with Drs.Tsunoda, National Institute of Animal Industry (NIAI) and Ushijima, Chiba Prefectural Farm Animal Center. The fruits of this technology were applied to the production of a calf from a cell of long-term-cultured inner cell mass (1998, Itoh et al, ZEN-NOH Central Research Institute for Feed and Livestock) and a cloned calf from three-successive-cloning (1997, Tsunoda et al.). According to the survey of MAFF of Japan, over 500 calves were born until this year and a half of them were already brought to the market for beef. 4. After the report of "Dolly", in February 1997, the first somatic cell clone female calves were born in July 1998 as the fruits of the joint research organized by Dr. Tsunoda in Kinki University (Kato et al, 2000). The male calves were born in August and September 1998 by the collaboration with NIAI and Kagoshima Prefecture. Then 244 calves, four pigs and a kid of goat were now born in 36 institutes of Japan. 5. Somatic cell cloning in farm animal production will bring us an effective reproductive method of elite-dairy- cows, super-cows and excellent bulls. The effect of making copy farm animal is also related to the reservation of genetic resources and re-creation of a male bull from a castrated steer of excellent marbling beef. Cloning of genetically modified animals is most promising to making pig organs transplant to people and providing protein drugs in milk of pig, goat and cattle.

• 농업과학연구
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• 제38권3호
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• pp.453-458
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• 2011

The MC1R (Melanocortin 1 receptor) gene has been known as a causative gene of the coat colors in mammals and responsible for the E (Extension) locus which has three alleles ($E^D$, $E^+$, e) that determines coat colors. The dominant allele $E^D$ produces black or brown colors due to the missense mutation and the recessive e allele has frameshift mutation which shows red or yellow coat colors. Whereas the wild type $E^+$ produces variety of colors due to the interaction with A (Agouti) locus. In this study, PCR-RFLP was performed using two restriction enzymes (BsrF I and MspA1 I) in order to obtain MC1R genotypes in Korean brindle cattle and black cattle. The results showed that all of the animals have the $E^+$ alleles, indicating the $E^+$ allele might related with black coat colors. Later on, the experiments expanded to the 260 Korean candidate bulls whether these animals have the same $E^+$ allele. Among 260 samples investigated, 5% (13/260) of the animals had $E^+$e genotypes, indicating the $E^+$ allele is also present in the candidate bulls in a low frequency. Even though we expected that A locus also affect the black coat color in cattle, all the black coat color animals (brindle and black) have $E^+$ alleles in this study. Therefore, the genotyping of the MC1R gene in candidate bulls will recommended be applied for eliminating of black coat colors in Hanwoo population, if the farmers need to have the brown coat colors only.

• Reproductive and Developmental Biology
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• 제35권3호
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• pp.377-383
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• 2011

본 연구에서는 제주흑우의 유전자원 보존과 증식을 위한 안정적인 동결정액 제조법을 수립하기 위하여 제주흑우의 정액 동결 제조에 있어 동결 융해 후 ethylene glycol이 정자의 운동성, 생존율 그리고 첨체에 미치는 영향에 대하여 알아보고자 수행하였다. 제주흑우의 동결정액제조시 5%의 ethylene glycol의 첨가가 $72.5{\pm}5.00%$의 활력과 $54.88{\pm}0.66%$의 생존율 그리고 $46.00{\pm}2.40%$의 정자막 온전성을 나타내 3%와 5%의 ethylene glycol을 첨가한 실험구보다 유의적으로 높은 결과를 나타냈다(p<0.05). 또한, 7% glycerol을 사용한 실험구와 비교하였을 때 5% ethylene glycol을 첨가하였을 때 유의적으로 높은 생존율과 정자막 온전성을 나타냈다(p<0.05). 또한, 예비 동결 조건이 정자의 성상에 미치는 영향에 있어서는 3 cm, 5분 예비동결 실험구에서 생존율과 정자막 온전성이 유의적으로 감소하였다(p<0.05). Ethylene glycol이 정자의 첨체 양상에 미치는 영향에 있어서는 5%와 7%의 ethylene glycol을 사용하였을 때 효과적으로 첨체가 보호되어 F pattern의 비율이 유의적으로 높게 나타났으며(p<0.05), 조기 첨체 반응도 유의적으로 낮은 수준을 보였다(p<0.05). 그러나 7%의 glycerol과 비교하였을 때는 유의적인 차이를 나타내지 않았으며, 5%와 7% ethylene glycol 사이의 유의적 차이도 나타나지 않았다. 예비 동결 조건이 정자의 첨체 양상에 미치는 영향에 있어서는 역시 정자의 생존율과 정자막 온전성과 같이 3 cm, 5분 예비동결 시 유의적인 F pattern의 감소와 조기 첨체 반응에 의한 AR paattern의 증가를 볼 수 있었다(p<0.05). 이와 같은 결과는 본 연구에서 사용된 ethylene glycol과 예비동결 조건의 조합으로 나타난 결과를 활용하여, 희소가축의 생식세포 보존 및 유전자원 확립을 위한 중요한 자료가 될 것이며, 생존율과 운동성 증대를 위한 다양한 희석제를 활용한 연구가 필요할 것으로 사료된다.

• Reproductive and Developmental Biology
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• 제34권3호
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• pp.127-134
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• 2010

This study was to investigate the effect of flavonoid treatment on in vitro development of bovine somatic cell nuclear transfer (SCNT) embryos, and their pregnancy and delivery rate after embryo transfer into recipient. In experiment 1, to optimize the flavonoid concentration, parthenogenetic day 2 ($\geq$ 2-cell) embryos were cultured in 0 (control), 1, 10 and $20\;{\mu}M$ flavonoid for 6 days. In the results, in vitro development rate was the highest in $10\;{\mu}M$ flavonoid group (57.1%) among treatment groups (control, 49.5%; $1\;{\mu}M$, 54.2%; $20\;{\mu}M$, 37.5%), and numbers of total and ICM cells were significantly (p<0.05) higher in $10\;{\mu}M$ flavonoid group than other groups. We found that $10\;{\mu}M$ flavonoid treatment can significantly (p<0.05) decrease the apoptotic index and derive high expression of anti-oxidant, anti-apoptotic, cell growth and development marker genes such as Mn-SOD, Survivin, Bax inhibitor, Glut-5, In-tau, compared to control group. In experiment 2, to produce the cloned Jeju Black Cattle, beef quality index grade 1 bull somatic cells were transferred into enucleated bovine MII oocytes and reconstructed embryos were cultured in $10\;{\mu}M$ flavonoid added medium. When the in vitro produced day 7 or 8 SCNT blastocysts were transferred into a number of recipients, $10\;{\mu}M$ flavonoid treatment group presented higher pregnancy rate (10.2%, 6/59) than control group (5.9%, 2/34). Total three cloned Jeju Black calves were born. Also, two cloned calves in $10\;{\mu}M$ flavonoid group were born and both were all healthy at present, while the one cloned calf born in control group was dead one month after birth. In addition, when the result of short tandem repeat marker analysis of each cloned calf was investigated, microsatellite loci of 11 numbers matched genotype between donor cell and cloned calf tissue. These results demonstrated that the flavonoid addition in culture medium may have beneficial effects on in vitro and in vivo developmental capacity of SCNT embryos and pregnancy rate.