http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
PCR-RFLP 시스템을 이용한 배 및 사과의 속간잡종 검정
김회택,평전풍,이인호,조광식,김윤경,강삼석,김명수,손동수,고갑천,노일섭 한국육종학회 2004 한국육종학회지 Vol.36 No.5
Through the intergeneric hybridization of pear ´apple, 137 seeds were successfully obtained. The average fruit setting showed about 12.0%. Eighty seeds were harvested from the combination of apple ´pear intergeneric crossing with the 6.4% of fruit setti
김회택,노일섭 한국원예학회 2016 원예과학기술지 Vol.34 No.3
The parentage of the horticulturally important pear cultivar ‘Niitaka’ was confirmed by determining its S -genotypes based on the S-RNase and PpSFBB-γ genes, and genotyping using simple sequence repeat (SSR) markers. Previous reports suggested that the cultivars ‘Amanogawa’ and ‘Imamuraaki’ were the parents of ‘Niitaka’, although the cultivars ‘Chojuro’ and ‘Shinchu’ were also examined as candidate parents, along with two other cultivars. In the present study, the S -genotype of ‘Niitaka’ was determined to be S 3S 9. The S 9-RNase of ‘Niitaka’ was found to be likely inherited from the parent ‘Amanogawa’ (S 1S 9) and the S 3-RNase from ‘Chojuro’ (S 3S 5) or ‘Shinchu’ (S 3S 5). Based on the S-genotypes, the cultivar ‘Imamuraaki’ (S 1S 6) had no contribution to the parentage of ‘Niitaka’ (S 3S 9). A total of 67 polymorphic SSR markers were used to further confirm the parentage of ‘Niitaka’. Discrepancies were found at several SSR loci between ‘Niitaka’ and the cultivars ‘Imamuraaki’ and ‘Shinchu’, whereas ‘Niitaka’ inherited alleles from ‘Amanogawa’ and ‘Chojuro’ at all SSR loci. Therefore, our findings established that ‘Amanogawa’ and ‘Chojuro’ are the parents of pear cultivar ‘Niitaka’, and not ‘Imamuraaki’ as previously reported.
국내 멜론 흰가루병균의 race 동정 및 시판품종의 흰가루병 저항성 판별
김회택,박종인,노일섭 한국식물생명공학회 2016 JOURNAL OF PLANT BIOTECHNOLOGY Vol.43 No.1
국내 멜론 및 박과채소 재배농가(안성, 이천, 영암, 창녕, 순천)에서 발병하고 있는 멜론 흰가루병균을 채집한 후흰가루병균의 형태학적 특성을 이용한 종류 구분 및 멜론 race 판별계통을 이용한 국내에서 발병하고 있는 흰가루병균의 race를 확인하였다. 그 결과 국내 멜론 흰가루병균의 종류는 Podosphaera xanthii (syn. Sphaerotheca fuliginea) 였으며, 기존에 보고된 race 1, N2, A와 판별결과가 일치하는 3 종류의 균주가 분리되었다. 또한 기존에 보고된race (1, N1, N2, A, S, 5)와 검정 결과가 다른 새로운 race 의 흰가루병균 2종이 동정되었다. 그리고 5개의 분리 및동정된 흰가루병균을 이용하여 국내 시판중인 멜론 15품종에 대한 저항성을 조사한 결과, race1에 대해서는 15품종 중 9품종이 저항성을 보였다. Race N2와 A대해서는소수의 품종에서 저항성을 보였으며, 새로운 race BN968 에서는 15품종 모두가 이병성을 나타내었다. 또한 멜론 흰가루병 race 1 저항성 DNA 마커 KPMR1M-1과 KPMR1M-2 에 의한 이병성 및 저항성 판별 결과와 race 1 접종 결과는 일치하였다. 따라서 국내 멜론 품종 육종에 있어서 다양한 race 특이적 마커 개발 및 이를 활용한 복합 race 저항성 품종 개발이 요구된다. Powdery mildew is an important disease of the melon (Cucumis melo L.). Seven isolates of powdery mildew fungi were collected from five locations in Korea; Anseong (DH487), Icheon (BN103, BN625, BN968), Yeongam (YA141), Changnyeong (CN582), and Suncheon (SN102). All 7 fungi had a similar trend of conidial chain and conidiophore development as Podosphaera xanthii with fibrosin bodies in mature conidia. Among them, 2 isolates of powdery mildew fungi; CN582 and SN102 showed similar responses to resistance against powdery mildew as the previously reported race 1 and race N2. The isolates YA141 and BN103 showed similar responses as like as race A. However, three isolates of powdery mildew fungi (BN625, BN968, and DH487) showed different responses compared to the previously reported races (1, N1, N2, A, S, and 5). Therefore, these three isolates could be designated as new races in melon. Nine out of 15 commercial melon cultivars in Korea showed resistance to race 1 (CN582). However, the new race BN968 invaded all 15 cultivars. Results of the two molecular markers were consistent in response to disease development by race 1 of Podosphaera xanthii in case of the above mentioned cultivars. This study confirmed the presence of new melon powdery mildew fungi in Korea which are similarly notorious as like as the previously reported race 1. Therefore, breeders can use these two molecular markers for breeding melon in Korea that is resistant to race 1 and as well as to some other races.
멜론 흰가루병의 race 분화 및 저항성 계통 선발을 위한 분자마커 개발
김회택,박종인,石川 友子,葛谷 真輝,堀井 学,八城 和敏,노일섭 한국식물생명공학회 2015 식물생명공학회지 Vol.42 No.4
Powdery mildew (Podosphaera xanthii) commonly occurs in cultivated fields of melon (Cucumis melo L.). It inflicts a lot of damages. Therefore, breeding resistant lines is essential. Development of a resistant line by integrating resistance gene takes a long time. In addition, break down of developed resistance by generating new virulent fungus strains increases disease susceptibility. This phenomenon was related to races of powdery mildew. Therefore, it is important to develop a DNA marker to genetically analyze race-specific resistance genes of melon powdery mildew to breed resistant lines. To date, a total of 28 races of Podosphaera xanthii have been reported in the literature. In Japan, 10 races have been reported in the Ibaraki region. We developed a system to characterize the races of Podosphaera xanthii and confirmed eight out of those 10 races in the Ibaraki region. In Korea, only one race has been characterized to date. However, some different races were detected. Through genetic analysis of resistant lines and susceptible lines of powdery mildew, resistance genes of race1 (Pm-X, PXB, and Pm-R 1), race N1 (PXA), race 2 (Pm-w and Pm-R 2), race 3 (Pm-X3), and race 5 (Pm-X5 and Pm-R5) were identified in melon. These related genes of race 1, 3, N1, 5, and race 1, 2, 5 were located at linkage group II and V, respectively. In race 1, resistance gene was located in the linkage group XII. In addition, each race-specific marker related to specific resistance gene was developed. Using race information and race selection system obtained in this study, resistant line can be bred to develop resistant cultivar for several areas. Furthermore, this will make it more easily and economically to breed resistant lines by using selected markers.
국내 멜론 흰가루병균의 race 동정 및 시판품종의 흰가루병 저항성 판별
김회택,박종인,노일섭,Kim, Hoy-taek,Park, Jong-in,Nou, Ill-sup 한국식물생명공학회 2016 식물생명공학회지 Vol.43 No.1
국내 멜론 및 박과채소 재배농가(안성, 이천, 영암, 창녕, 순천)에서 발병하고 있는 멜론 흰가루병균을 채집한 후 흰가루병균의 형태학적 특성을 이용한 종류 구분 및 멜론 race 판별계통을 이용한 국내에서 발병하고 있는 흰가루병균의 race를 확인하였다. 그 결과 국내 멜론 흰가루병균의 종류는 Podosphaera xanthii (syn. Sphaerotheca fuliginea)였으며, 기존에 보고된 race 1, N2, A와 판별결과가 일치하는 3 종류의 균주가 분리되었다. 또한 기존에 보고된 race (1, N1, N2, A, S, 5)와 검정 결과가 다른 새로운 race의 흰가루병균 2종이 동정되었다. 그리고 5개의 분리 및 동정된 흰가루병균을 이용하여 국내 시판중인 멜론 15품종에 대한 저항성을 조사한 결과, race1에 대해서는 15품종 중 9품종이 저항성을 보였다. Race N2와 A대해서는 소수의 품종에서 저항성을 보였으며, 새로운 race BN968에서는 15품종 모두가 이병성을 나타내었다. 또한 멜론 흰가루병 race 1 저항성 DNA 마커 KPMR1M-1과 KPMR1M-2에 의한 이병성 및 저항성 판별 결과와 race 1 접종 결과는 일치하였다. 따라서 국내 멜론 품종 육종에 있어서 다양한 race 특이적 마커 개발 및 이를 활용한 복합 race 저항성 품종 개발이 요구된다. Powdery mildew is an important disease of the melon (Cucumis melo L.). Seven isolates of powdery mildew fungi were collected from five locations in Korea; Anseong (DH487), Icheon (BN103, BN625, BN968), Yeongam (YA141), Changnyeong (CN582), and Suncheon (SN102). All 7 fungi had a similar trend of conidial chain and conidiophore development as Podosphaera xanthii with fibrosin bodies in mature conidia. Among them, 2 isolates of powdery mildew fungi; CN582 and SN102 showed similar responses to resistance against powdery mildew as the previously reported race 1 and race N2. The isolates YA141 and BN103 showed similar responses as like as race A. However, three isolates of powdery mildew fungi (BN625, BN968, and DH487) showed different responses compared to the previously reported races (1, N1, N2, A, S, and 5). Therefore, these three isolates could be designated as new races in melon. Nine out of 15 commercial melon cultivars in Korea showed resistance to race 1 (CN582). However, the new race BN968 invaded all 15 cultivars. Results of the two molecular markers were consistent in response to disease development by race 1 of Podosphaera xanthii in case of the above mentioned cultivars. This study confirmed the presence of new melon powdery mildew fungi in Korea which are similarly notorious as like as the previously reported race 1. Therefore, breeders can use these two molecular markers for breeding melon in Korea that is resistant to race 1 and as well as to some other races.
김회택,Shigeki Moriya,Kazuma Okada,Kazuyuki Abe,박종인,Toshiya Yamamoto,노일섭 한국식물생명공학회 2016 JOURNAL OF PLANT BIOTECHNOLOGY Vol.43 No.1
We isolated and confirmed two S-RNases, denoted as mpS1 and mpS2, from apple rootstock ‘Marubakaido’ (Malus prunifolia Borkh. Var. ringo Asami). These S-RNases contained and conserved five cysteine residues and two histidine residues, which are essential for RNase activity. The mpS1 showed high similarity to S5 (99.1%) of Malus spectabilis, whereas the mpS2 showed 99.5% nucleotide sequence similarity to S26 of (Malus × domestica) and 99.6% to S35 of (Malus sieversii) when compared with reported S-RNases. In amino acid sequences, the mpS1-RNase was almost similar to the S5-RNase of Malus spectabilis, and the mpS2-RNase was similar to the S35 of Malus sieversii, with only one bp being different from the S26-RNase of Malus × domestica. The 57 S-RNases of Malus species were renamed and rearranged containing the new S-RNases, as mprpS35 (mpS2) and mprpS57 (mpS1), for determining S-genotypes and identifying new alleles from apple species (Malus spp.).