• 제목/요약/키워드: inheritance pattern

검색결과 82건 처리시간 0.031초

제주마에서 총마 모색의 유전 양성과 후보 유전좌위의 유전적 다형성 (Genetic Polymorphisms of Candidate Loci and Inheritance Ppatterns of Gray Coat Color in Jeju Horses.)

  • 한상현;이종언;김남영;고문석;정하연;이성수
    • 생명과학회지
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    • 제19권6호
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    • pp.793-798
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    • 2009
  • 본 연구는 제주마에서 빈번하게 관찰되는 전신성 백모색 발생의 유전 양상과 유전적 변이와의 상관을 구명하기 위해 수행하였다. 백모색은 표현형과 MC1R 유전자형 분석 자료의 조합을 근거로 결정한 가라, 유마, 적다 등 모든 기본 모색에서 관찰되었다. 제주마에서는 타 품종들에서 KIT 유전자의 이형 접합성에 의해 발생하는 선천성 백색에 대한 잠재적 돌연변이 들은 발견되지 않았다. STX17 유전자의 intron 6 에서 4.6-kb 중복을 보유한 개체들에서 특이적으로 탈색된 백모색이 관찰되었다. 관찰기록과 STX17 유전자형에 따라 제주마에서 관찰되는 탈색된 백화현상은 총마(점진적 백화증, Gray) 로 확인되었다. 가계도 분석에서 총마 형질은 상동염색체성 우성유전형 질로 나타났으며 상동염색체성 열성형질인 albinism과도 구분되었다. 제주마에서 총마 모색이 자마 시기에는 명확하게 발현되는 않으며, 종종 다른 표현형들과 혼동을 일으키기도 하기 때문에, 총마와 이와 유사한 표현형으로 출생 시부터 혼합 모색을 나타내는 조모색, 상처 치료 후 백화, 백반 유사피부 백색증 등에 대한 추가 연구가 요구된다고 하겠다. 그럼에도 불구하고 총마와 유전적 배경의 관계를 구명한 본 연구결과는 제주마에서 분자육종을 위한 유용한 정보를 제공할 것으로 사료된다.

배유 특이 프로모터에 의해 유도된 GUS 유전자의 형질전환 담배 내에서의 발현 및 유전 양상 (Expression and Inheritance Patterns of Gus Gene Driven by an Endosperm-Specific Promoter in Transgenic Tobacco)

  • 박영두;김형석
    • 원예과학기술지
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    • 제18권5호
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    • pp.594-598
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    • 2000
  • 본 실험은 형질전환 담배내에서의 배유 특이 promoter에 의한 gus 유전자의 조직 특이적 발현 여부와 전이유전자의 후대로의 유전 양상을 확인하고자 수행하였다. 배유 특이 promoter에 의해 유도되는 gus 유전자(Z4pro-gus)와 kanamycin 저항성유전자를 운반하는 BV3 construct를 A. tumerfaciens을 이용하여 담배 형질전환체를 유기시켰다. 형질전환체 중에서 8개체를 선발하여 nptII primer를 이용하여 PCR을 실시한 결과 8개체 모두에서 700bp의 PCR 산물을 얻을 수 있었다. Promoter에 따른 유전자의 발현양상을 알아보기 위하여 Z4pro-gus가 전이된 형질전환체의 잎과 CaMV35S와 gus 유전자(35Spro-gus)로 구성된 pBI121 construct를 전이시킨 형질전환체의 잎으로부터의 발색정도를 비교하였다. 그 결과 Z4pro-gus가 전이된 형질전환체의 경우 잎에서 매우 부분적으로 극소량 발색되었으나 35Spro-gus가 전이된 형질전환체의 잎에서는 상대적으로 많은 양의 발색정도를 보여 promoter에 따른 발현정도의 차이를 보였다. 보다 명확한 Z4 promoter의 조직 특이 발현 양상을 확인하기 위하여 Z4pro-gus로 형질전환시킨 $T_0$ 식물체를 자가수분하여 얻은 $R_1$ 종자와 35Spro-gus를 형질전환시켜 같은 방법으로 얻은 $R_1$ 종자를 histochemical assay하였다. 그 결과 35Spro-gus로 형질전환된 담배 종자는 절단면 전체에서 gus 유전자가 발현되어 배유뿐만 아니라 종자 내 다른 조직에서도 발색되는 양상을 나타내었으나 Z4pro-gus를 형질전환 시켜 얻은 종자의 경우는 배유 부분만이 조직 특이적으로 파랗게 발색되었고 배 또는 그 이외의 조직에서는 gus 발색이 전혀 관찰되지 않았다. Kanamycin 저항성검정을 실시한 결과 모든 계통에서 전이유전자가 후대로 안정적으로 전이됨을 확인할 수 있었다.

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Studies on Boil-off Loss Ratio in the Cocoon Shells of Multivoltine${\times}$Bivoltine Hybrids of Silkworm, Bombyx mori L.

  • Rao, D.Raghavendra;Singh, Ravindra;Premalatha, V.;Sudha, V.N.;Kariappa, B.K.;Dandin, S.B.
    • International Journal of Industrial Entomology and Biomaterials
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    • 제8권1호
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    • pp.101-106
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    • 2004
  • The process of removal of gummy proteinous material sericin from silk is commonly called as degumming loss or boil-off loss ratio. In the present study, the boil-off loss ratio in the cocoon shells of twelve multivoltine${\times}$bivoltine hybrids and their parents were analysed. Inheritance pattern of boil-off loss ratio was analysed in crosses involving high and low boil-off loss parents, F$_1$s, F$_2$s and back-crosses by parent off spring regression analysis. Heterosis and heterobeltiosis was also analysed for this character, Highly significant (P>0.01) variations were observed in eight out of ten multivoltine and two out of five bivoltine parents indicating the presence of genetic variation in the expression of boil-off loss ratio. Among F$_1$ hybrids, ten hybrids expressed significant (P>0.01) variations when compared with control hybrid PM${\times}$NB$_4$D$_2$. Significant negative heterosis was expressed in three multi ${\times}$ bi hybrids viz., BL67${\times}$CSR$_{101}$, 96A${\times}$CSR$_{19}$ and 96C${\times}$CSR$_{19}$, which is desirable for this character, whereas expression of heterobeltiosis was significant only with one hybrid, 96C${\times}$CSR$_{18}$ in desired direction. Studies on inheritance pattern showed that the character is heritable and contribution percentage of female and male in the ratio of 50.9: 49.1 and it appears that both the parents are influencing in the expression of boil-on loss ratio in silkworm. Based on the overall performance and evaluation by multiple trait evaluation index and also considering the expression of the boil-off loss ratio three hybrids vix., BL67 ${\times}$ CSR$_{101}$, 96A${\times}$CSR$_{19}$ and 96C${\times}$CSR$_{18}$ were found superior and recommended for commercial exploitation.n.ion.n.

Evaluation of coat color inheritance and production performance for crossbreed from Chinese indigenous Chenghua pig crossbred with Berkshire

  • Li, Yujing;Yuan, Rong;Gong, Zhengyin;Zou, Qin;Wang, Yifei;Tang, Guoqing;Zhu, Li;Li, Xuewei;Jiang, Yanzhi
    • Animal Bioscience
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    • 제35권10호
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    • pp.1479-1488
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    • 2022
  • Objective: This work was to determine coat inheritance and evaluate production performance for crossbred pigs from Berkshire×Chenghua (BC) compared with Chinese indigenous Chenghua (CH) pigs. Methods: The coat color phenotypes were recorded for more than 16,000 pigs, and the genotypes of melanocortin 1 receptor (MCIR) gene were identified by sequencing. The reproductive performance of 927 crossbred BC F4 gilts and 320 purebred CH gilts was recorded. Sixty pigs of each breed were randomly selected at approximately 60 days of age to determine growth performance during fattening period, which lasted for 150 days for BC pigs and 240 days for CH pigs. At the end of the fattening period, 30 pigs of each breed were slaughtered to determine carcass composition and meat quality. Results: The coat color of BC pigs exhibits a "dominant black" hereditary pattern, and all piglets derived from boars or sows genotyped ED1 ED1 homozygous for MC1R gene showed a uniform black coat phenotype. The BC F4 gilts displayed a good reproductive performance, showing a higher litter and tear size and were heavier at farrowing litter and at weaning litter than the CH gilts, but they reached puberty later than the CH gilts. BC F4 pigs exhibited improved growth and carcass characteristics with a higher average daily live weight gain, lower feed-to-gain ratio, and higher carcass lean meat rate than CH pigs. Like CH pigs, BC F4 pigs produced superior meat-quality characteristics, showing ideal pH and meat-color values, high intramuscular fat content and water-holding capacity, and acceptable muscle-fiber parameters. C18:1, C16:0, C18:0, and C18:2 were the main fatty acids in M. longissimus lumborum in the two breeds, and a remarkably high polyunsaturated/saturated fatty acid ratio of ~0.39 was observed in the BC F4 pigs. Conclusion: The BC F4 pigs exhibit a uniform black coat pattern and acceptable total production performance.

Leopard danio 반문의 유전 양상과 생존율에 미치는 영향 (Genetic Analysis of Pigmentation Pattern in the Leopard Danio)

  • 이병문;강거영;송춘복
    • 한국양식학회지
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    • 제11권3호
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    • pp.353-361
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    • 1998
  • Zebra danio와 leopard danio의 부모세대(Po)간의 상반교재를 병행한 교배실험에서 5개체의 small spotted type이 출현한 1개의 실험구를 제외하고는 모두 wild type으로 나타났다. 그리고 F하(1)세대 간의 상반교배로 태어난 F하(2)세대는 wild type과 spotted type의 비율이 모두 3 : 1로 나타났다. F하(1)세대와 Po세대와의 상반교배를 병행한 역교배실험에서는 부모세대를 zebra danio로 사용한 경우, wild type과 spotted type이 178 : 1, 2.7 : 1, 3.9 : 1로 출현하는 실험구를 제외하고는 모두 wild type으로 나타났고, spotted type을 사용한 역교배 및 검정교배실험에서 40개체의 small spotted type으로 출현하는 실험구를 제외하고는 모두 1 : 1의 비율을 나타내었다. Z x F(LZ) 교재실험구 중 두 개의 반복구(각각 2.7 : 1, 3.9 : 1 )에서 wild type과 spotted type의 비율이 3 : 1로 나타났으나, F하(1)세대간의 교배실험과 검정교배실험 결과, zebra danio 암컷이 이형접합자(Pp)였다고 추정되었다. Spotted type과 small spotted type으로 나타나는 예외적인 결과에 대해 아직까지 확실히 규명되지 않았지만, 모든 결과를 종합해 볼 때 반문을 조절하는 유전자의 인자형은 zebra danio가 동형 우성 (PP)이고, leopard danio가 동형 열성(pp)이며, 유전자는 상염색체 상에 존재한다는 것을 알 수 있었다. 수정 후부터 15일째까지의 생존율 비교 실험에서 $Z{\times}Z$ (83.8${\pm}$6.7%)와 $L{\times}L$(80.6${\pm}$4.8%)는 생존율에 있어서 그 차이가 통계적으로 유의하지 않았으며, 이들과 다른 교배군인 $Z{\times}L$(73.2${\pm}$2.0%) 이나 $L{\times}Z$(70.6${\pm}$4.2%) 와는 유의차를 보였다. 따라서 D. frankei로 알려졌던 leopard danio는 zebrafish의 aquarium morph인 반문 돌연변이체이지만 leopard danio 사이에 교배가 이루어질 경우에는 유전적으로 안정되어 있음을 알 수 있는 반면에, wild type zebrafish와는 다소의 유전적인 부조화가 존재한다고 추정된다.

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가족성 섬유성 이형성증(Cherubism)에 대한 고찰 (A REVIEW ON CHERUBISM)

  • 김경덕;김신;정태성
    • 대한소아치과학회지
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    • 제24권4호
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    • pp.751-757
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    • 1997
  • Cherubism is an uncommon, benign fibrosseous lesion of the jaws that causes a progressive, painless, symmetrical expansion of the maxilla and mandible. It's autosomal dominance pattern of inheritance has been confirmed. A characteristic deformity is specific to this disease: hypertrophy of the mandible, swelling of cheeks and sometimes hypertrophy of maxilla with eyes tending to look up ; that looks like the Renaissance cherubs. It usually makes figures during childhood between 2-4 years of age and progresses until puberty, after which it spontaneously regresses 10 most cases. As a result of this case review, the management strategies for cherubismic children in standpoint of pediatic dentistry can be summarized as follows: 1. It can be detected early in childen through its characteristic clinical and radiographic features, which is confirmed by histopathological examination and familial history. 2. The supervision of arch space is required against its frequent sequelae, the early missing of primary teeth and eruption disorders of permanent teeth. 3. It is highly recommended to continue the periodic check-up with clinical and radiographic examination, leading to surgical intervention in cases of aggravation.

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A novel mutation in GJC2 associated with hypomyelinating leukodystrophy type 2 disorder

  • Komachali, Sajad Rafiee;Sheikholeslami, Mozhgan;Salehi, Mansoor
    • Genomics & Informatics
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    • 제20권2호
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    • pp.24.1-24.8
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    • 2022
  • Hypomyelinating leukodystrophy type 2 (HLD2), is an inherited genetic disease of the central nervous system caused by recessive mutations in the gap junction protein gamma 2 (GJC2/GJA12). HLD2 is characterized by nystagmus, developmental delay, motor impairments, ataxia, severe speech problem, and hypomyelination in the brain. The GJC2 sequence encodes connexin 47 protein (Cx47). Connexins are a group of membrane proteins that oligomerize to construct gap junctions protein. In the present study, a novel missense mutation gene c.760G>A (p.Val254Met) was identified in a patient with HLD2 by performing whole exome sequencing. Following the discovery of the new mutation in the proband, we used Sanger sequencing to analyze his affected sibling and parents. Sanger sequencing verified homozygosity of the mutation in the proband and his affected sibling. The autosomal recessive inheritance pattern was confirmed since Sanger sequencing revealed both healthy parents were heterozygous for the mutation. PolyPhen2, SIFT, PROVEAN, and CADD were used to evaluate the function prediction scores of detected mutations. Cx47 is essential for oligodendrocyte function, including adequate myelination and myelin maintenance in humans. Novel mutation p.Val254Met is located in the second extracellular domain of Cx47, both extracellular loops are highly conserved and probably induce intramolecular disulfide interactions. This novel mutation in the Cx47 gene causes oligodendrocyte dysfunction and HLD2 disorder.

한국 전통복식 상의(上衣)류의 구조적인 특징을 활용한 셔츠디자인개발 - 패션문화상품을 중심으로 - (The Development of Shirt Design Utilizing the Structural Characteristics of Traditional Korean upper Garments - Focusing on Fashion Cultural Products -)

  • 최은주
    • 한국의류산업학회지
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    • 제25권4호
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    • pp.439-448
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    • 2023
  • Korea's original traditional costume designs have a great potential to be re-imagined from a global perspective and developed into high-value-added fashion culture products that can enter the international market. This study applied the structural features of traditional clothing to the design of fashion cultural products. This study developed designs using Beja, Sagyusam, Aekjuem-po, Danlyeong, Cheolrik, Jang-jegori of Korea. To the best of our knowledge, this study is the first to conduct a literature survey of traditional Korean clothing. We designed shirts using Adobe Illustrator and created a pattern with the Yuka program. This design was applied to a three dimensional virtual dressing system called CLO. A survey of individual interest in developed fashion cultural products was also conducted. The shirt designs were obtained by applying the details and structural characteristics of traditional Korean clothing. Among the six shirt designs, when asked which design would be suitable for wearing, gifting, or uniform, the shirts with the design of Danlyeong, Beja, and Sagyusam were generally highly preferred. This study can be used as basic data for the global market for fashion cultural products, and can contribute to the inheritance and development of culture and tradition by maintaining Korea's uniqueness in the modern global era and increasing tourism revenue.

이상자녀수(理想子女數) 및 자녀(子女)에 대(對)한 가치관(價値觀) 변천(變遷)에 관(關)한 연구(硏究) (Study on Changes of Attitude toward Ideal Number of Children and Value System for Children)

  • 김영봉
    • Journal of Preventive Medicine and Public Health
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    • 제7권1호
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    • pp.203-209
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    • 1974
  • This study is intended to comparison of the recent ideal number of children and atrial approach for analyzing value system for children that form attitude affecting birth control with earlier study conducted 10 years ago. In general the traditional fertility pattern of Korea may be considered as 'early marriage and high fertility' backed by the confucian value system of a farming-oriented country. A selective attitude favoring sons contributes substantially to fertility. But Korea is now moving toward a late marriage and fertility pattern. This has been due to the repid introduction of western culture and a partial acceptance of western value systems, a relative weakening of traditional value systems, a gradual increase in infant and child servival rates thresh medicines, and a desire to avoid having too many children because of economic poverty. This study showed following results: Ideal number of sons and daughters in urban area was decreased by 0.2 respectively compared to earlier study. In rural area, the number of decrease of sons and daughters was 0.5 and 0.2 respectively. The conception concerning Happiness has changed to wealth from health in previous opinion. Regarding attitude toward having sons, 98 percent of them wanted to have sons positively, moreover 10 percent of them wanted two or more sons. Regarding reasons for the wanting sons, we see that economic and traditional considerations, such as dependance in old age, and inheritance of the family line, are a principle concern of about 56 percent in both areas. The rate of dependence in old age was decreased conspicuously compare to previous study while the rate of helding rituals was increased remarkably in rural area. Among reasons for limiting family size. 'for better living and for better education for their children were main rasons reted 46 percent in urban, 51 percent in rural areas. The rates were not changed compare to previous study. Regarding attitude of those who have no son or children, the rate of re-marriage with second wife was decreased remarkably in rural area and the rate of living without special behaivor for having son was increased compare to previous study.

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소나무의 몇가지 다형적(多形的) 동위효소(同位酵素)의 유전분석(遺傳分析)(II) - Acid phosphatase, alcohol dehydrogenase와 catalase 동위효소(同位酵素)의 유전양식(遺傳樣式) - (Genetic Analysis of Some Polymorphic Isozymes in Pinus densiflora(II) - Inheritance of acid phosphatase, alcohol dehydrogenase and catalase isozymes -)

  • 김진수;홍용표
    • 한국산림과학회지
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    • 제68권1호
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    • pp.32-36
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    • 1985
  • 소나무의 acid phosphatase (ACP), alcohol dehydrogenase (ADH)와 catalase (CAT) 동위효소(同位酵素) 유전양식(遺傳樣式)을 구명(究明)하기 위하여 배유조직(胚乳組織)을 수평식 감자전분 전기영동법에 의하여 분석(分析)하였다. ACT 동위효소(同位酵素)는 최소한 3~4개의 지역(地域)으로 분리(分離)되었으나 분리가 잘된 ACP-A 지역(地域)의 동위효소(同位酵素)만이 분석(分析)되었다. ACP-A 지역(地域)에서 관찰된 5개(A1-A5)의 동위효소(同位酵素) 표현형(表現型)들은 공히 Mendel의 분리비(分離比)를 보여 이들이 각각 ACP-A 유전자좌(遺傳子座)에 존재(存在)하는 5개의 대립유전자(對立遺傳子)에 의해 지배받고 있음을 알 수 있었다. 2개의 ADH 지역(地域)이 (ADH-A와 ADH-B) 분리(分離)되었으나, 양극(陽極)으로의 이동(移動)속도가 빠른 ADH-A 지역(地域)에서는 분석(分析)에 사용된 재료(材料)에서 변이(變異)가 발견(發見)되지 않았다. ADH-B 지역(地域)에서는 3개의 동위효소(同位酵素) 표현형(表現型) (B1-B3)들이 관찰되었고 이들이 공히 1:1의 분리비를 보여 ADH-B 유전자좌(遺傳子座)에 존재하는 3개의 대립유전자(對立遺傳子)에 의해 지배됨이 추정되었다. 수개의 band로 구성된 5개의 동위효소(同位酵素) 표현형(表現型)이 CAT에서 관찰되었으며, 이형접합성(異型接合性)인 모수(母樹)에서 이들 표현형간(表現型間)의 분리(分離)가 1:1 분리비(分離比)로부터 편차(偏差)를 보이지 않았으므로, 소나무에 있어서 CAT 동위효소(同位酵素)는 5개의 대립유전자(對立遺傳子)가 존재(存在)하는 하나의 유전자좌(遺傳子座)에 의해 지배되는 것으로 추정하였다.

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