• International Journal of Industrial Entomology and Biomaterials
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• 제8권1호
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• pp.113-115
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• 2004

Six generations (P$_1$, P$_2$, F$_1$, BC$_1$, BC$_2$ and F$_2$) of four bivoltine silkworm crosses (SKAU-R-1 ${\times}$ Yakwei, SKAU-R-6 ${\times}$ Yakwei, CSR$_2$ ${\times}$ CSR$_4$ and SH$_{6}$${\times}$ NB$_4$D$_2$) were evaluated in a completely randomized block design with 5 replications for each treatment. The generation mean 2 in respect of 3 metric traits (single cocoon weight, single shell weight, and shell ratio ％), were subjected to Cavallis joint scaling test. Additive dominance model was found to be adequate in CSR$_2$${\times}$CSR$_4$ and SH$_{6}$${\times}$ NB$_4$D$_2$ for single cocoon weight and shell weight and SKAU-R-6 ${\times}$ Yakwei for shell ratio(％). Whereas, in rest of the crosses epistasis was evident in the traits under investigation. Magnitude of additive gene effect (d) was greater than dominance(h) in SH$_{6}$${\times}$NB$_4$D$_2$ and SKUA-R-6${\times}$Yakwei for shell ratio (％) and in CSR$_2$${\times}$ CSR$_4$ for shell weight. Thus selection for these traits in early segregating generations of these crosses would be effective for obtaining considerable genetic gain. gain.

• Journal of Animal Science and Technology
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• 제53권3호
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• pp.185-193
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• 2011

To investigate the influences of candidate genes on the birth weight and the early stages of life, genotyping of the prolactin receptor 3 (PRLR3) and retinol-binding protein 4 (RBP4) genes was performed in 156 and 141 Berkshire pigs, respectively. The frequency of both PRLR3 alleles A and a was 0.50. The frequencies of the RBP4 alleles B and b were 0.42 and 0.58, respectively. Neither locus was in Hardy-Weinberg equilibrium. No significant associations of the PRLR3 alleles with birth or weaning weights and of the RBP4 alleles with birth weight were observed. The proportions of the phenotype variances due to the genotypes of PRLR3 in the feeder weights was 4.0% and those of RBP4 in the weaning and feeder weights were 11.9 and 3.3%, respectively (P < 0.05). The dominance effect of PRLR3 and RBP4 on feeder weights was 2.40 and -1.86 kg, respectively (P < 0.01). The additive and dominance effects of RBP4 on weaning weights were 0.332 and -0.682 kg, respectively (P < 0.01). Even if no significant epistasis of PRLR3 and RBP4 was detected, a considerable trend of consistent positive epistasis estimates of AA/BB and Aa/Bb was observed for all traits. The results of this study may have a considerable impact on early-stage growth by both loci, and a selection strategy should be designed separately for each marker in Berkshire pigs.

• 한국지능시스템학회논문지
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• 제15권6호
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• pp.661-667
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• 2005

본 논문에서는 서열순서화문제를 위한 새로운 혼합형 유전알고리즘을 제안한다. 제안된 유전알고리즘에서는 보로노이양자 화교차를 교차연산자로 사용하고 경로보전 3-최적화를 지역탐색 휴리스틱으로 사용한다. 보로노이양자화교차는 주어진 문제 인스턴스의 상위 정보를 이용하는 교차연산자이다. 이것은 원래 순회판매원문제를 위해서 제안된 교차연산자이기 때문에 서열순서화문제에 적용하기 위해서는 상당한 변형을 필요로 한다. 본 연구에서는 서열순서화문제에 맞도록 보로노이양자화교차를 적절히 변형하고, 변형된 보로노이양자화교차에서 필요로 하는 가능해생성알고리즘, 선행관계사이클분해알고리즘, 유전자거리지정방법 등을 개발하였다. TSPLIB와 ZIB-MP-Testdata로부터 얻어진 서열순서화문제 인스턴스들에 대한 실험결과, 제안된 유전알고리즘이 비교된 다른 유전알고리즘들에 비해서 더 안정적이고 성능이 우수한 것으로 나타났다.

• 한방안이비인후피부과학회지
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• 제18권2호
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• pp.118-123
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• 2005

Epistaxis is the condition which the blood comes out with the nose. It has been known that nasal bleeding happens with many reasons. In most cases, epistaxis is a slight illness, but sometimes, it leads to death because of longstanding or copious bleeding. First of all, to stop a hemorrhage is most important treatment for epistaxis, but the curative effect of oriental medical treatment for epistaxis does not become known well. We treated a patient suffered from epistasis with acupuncture, herb medication. After treatment we observed the improvement. Based on this study, it is considered that oriental medical treatment can be applied to the management of epistaxis.

• 전기학회논문지
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• 제57권9호
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• pp.1636-1641
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• 2008

In this study, we introduce a new approach to Parallel Genetic Algorithms (PGA) which combines AHFCGA with crossover operator. As to crossover operators, we use three types of the crossover operators such as modified simple crossover(MSX), arithmetic crossover(AX), and Unimodal Normal Distribution Crossover(UNDX) for real coding. The AHFC model is given as an extended and adaptive version of HFC for parameter optimization. The migration topology of AHFC is composed of sub-populations(demes), the admission threshold levels, and admission buffer for the deme of each threshold level through succesive evolution process. In particular, UNDX is mean-centric crossover operator using multiple parents, and generates offsprings obeying a normal distribution around the center of parents. By using test functions having multimodality and/or epistasis, which are commonly used in the study of function parameter optimization, Experimental results show that AHFCGA can produce more preferable output performance result when compared to HFCGA and RCGA.

• The Plant Pathology Journal
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• 제30권2호
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• pp.188-194
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• 2014

A comprehensive study was conducted using PPSMV resistant (BSMR 736) and susceptible (ICP 8863) genotypes to develop a segregating population and understand the inheritance of PPSMV resistance. The observed segregation was comparable to 13 (susceptible): 3 (resistant). Hence, the inheritance was controlled by two genes, SV1 and SV2, with inhibitory gene interaction.

• 한국작물학회지
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• 제43권3호
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• pp.135-140
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• 1998

Diallel analysis was conducted with FI's derived from crossing in all combinations without reciprocals among six rice varieties; three tropical japonica and three temperate japonica varieties, with different traits associated with panicle and flag leaf. Epistasis was observed in the number of primary branches (PB) per panicle and of spikelets per panicle, while flag leaf length, flag leaf color, PB length and neck node thickness were explained with the additive-dominance model. The estimated genetic mode of flag leaf length and PB length was a positive complete dominance model with high heritability, and that of flag leaf color and neck node thickness was an incomplete dominance model. In particular, tropical japonica varieties with low-tillering and heavy-panicle appear to have higher number of dominant genes for flag leaf length and PB length than temperate japonica varieties.

• 생명과학회지
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• 제28권4호
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• pp.398-407
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• 2018

벼 자색 종자과피(Purple pericarp, Prp) 형질은 주요 생리활성물질인 안토시아닌 C3G 생성에 관여하며 흑미를 결정하는 주요 유전형질이다. Prp 유전형질을 가진 흑미와 종자과피에 색이 없는 벼를 교배할 경우 그 후대는 검정색, 갈색, 백색이 각각 9:3:4로 분리된다. 1921년 Nagai에 의하여 제시된 바 벼 종자 색의 9:3:4 유전분리비로 인하여 벼 Prp 형질은 유전자의 열성상위(recessive epistasis) 현상으로 해석되었다. 그러나 흑미를 결정하는 Prp 형질은 두 개의 상보적 유전자들의 상호관계(complementary gene interaction)에 의한 것이기도 하다. 본 연구에서는 이러한 논란이 발생되는 이유를 설명하기 위하여 두 유전자의 조성이 완전한 이형접합인 Pbpb Pppp 유전자형을 가진 $F_1$ 잡종을 만들었다. 이들의 자손은 진한자색(검정), 중간자색, 갈색, 백색 종자이며 각각 3:6:3:4로 분리되었다. 즉, 검정색, 갈색, 백색의 종자가 각각 9:3:4의 비율로 분리된다. 그러나 생화학적인 분석결과 이들은 안토시아닌 중 cyanidin 3-O-glucoside (C3G)가 축적된 검정색 종자와 C3G가 없는 갈색 또는 백색 종자인 두 개의 집단을 분리되며 정확히 9:7의 분리 비를 갖는다. 이 경우 벼 Prp 형질을 갖는 검정쌀 또는 흑미는 전형적인 상보적 유전자의 상호관계에 의한 유전현상이다. 즉, 흑미의 자색 종피 형질 발현에는 Pb 유전자와 Pp 유전자에서 각각 한 개 이상의 우성대립인자의 발현이 필요하다. 그러나 Pb 유전자만 우성대립인자가 존재하는 Pb_ pppp 유전자형의 벼는 C3G를 생성하지 못하고 갈색 종자과피(Brown pericarp, Brp) 형질을 갖게 된다. 즉 갈색쌀는 우성 Pb 유전자의 우성대립인자에 의하여 결정된다. 그러므로 종피색을 결정하는 Prp 형질의 유전양상은 열성상위 현상으로 보이나 흑미의 결정요소인 안토시아닌 C3G의 함유 여부에 관한 유전분석을 시행하면 9:7의 비율로서 전형적인 두 개의 유전자가 모두 관여하는 상보적 유전현상이다. 유전적 정의는 유전자의 최종산물에 의한 물리적 또는 화학적 결정이다. 그러므로 결론하여 검정 쌀의 주요 생리활성물질인 안토시아닌 C3G 생성에 관한 유전현상은 Pb와 Pp 유전자의 상보적 유전자의 상호에 의한 것이다.

• Asian-Australasian Journal of Animal Sciences
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• 제22권1호
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• pp.124-130
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• 2009

Estimating genetic interaction effects in animal genomics would be one of the most challenging studies because the phenotypic variation for economically important traits might be largely explained by interaction effects among multiple nucleotide sequence variants under various environmental exposures. Genetic improvement of economic animals would be expected by understanding multi-locus genetic interaction effects associated with economic traits. Most analyses in animal breeding and genetics, however, have excluded the possibility of genetic interaction effects in their analytical models. This review discusses a historical estimation of the genetic interaction and difficulties in analyzing the interaction effects. Furthermore, two recently developed methods for assessing genetic interactions are introduced to animal genomics. One is the restricted partition method, as a nonparametric grouping-based approach, that iteratively utilizes grouping of genotypes with the smallest difference into a new group, and the other is the Bayesian method that draws inferences about the genetic interaction effects based on their marginal posterior distributions and attains the marginalization of the joint posterior distribution through Gibbs sampling as a Markov chain Monte Carlo. Further developing appropriate and efficient methods for assessing genetic interactions would be urgent to achieve accurate understanding of genetic architecture for complex traits of economic animals.

• Genomics & Informatics
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• 제14권4호
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• pp.160-165
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• 2016

Over the past decade, the detection of gene-gene interactions has become more and more popular in the field of genome-wide association studies (GWASs). The goal of the GWAS is to identify genetic susceptibility to complex diseases by assaying and analyzing hundreds of thousands of single-nucleotide polymorphisms. However, such tests are computationally demanding and methodologically challenging. Recently, a simple but powerful method, named "BOolean Operation-based Screening and Testing" (BOOST), was proposed for genome-wide gene-gene interaction analyses. BOOST was designed with a Boolean representation of genotype data and is approximately equivalent to the log-linear model. It is extremely fast, and genome-wide gene-gene interaction analyses can be completed within a few hours. However, BOOST can not adjust for covariate effects, and its type-1 error control is not correct. Thus, we considered two-step approaches for gene-gene interaction analyses. First, we selected gene-gene interactions with BOOST and applied logistic regression with covariate adjustments to select gene-gene interactions. We applied the two-step approach to type 2 diabetes (T2D) in the Korea Association Resource (KARE) cohort and identified some promising pairs of single-nucleotide polymorphisms associated with T2D.