• 제목/요약/키워드: spontaneous mutation

검색결과 48건 처리시간 0.02초

Homocysteine 과다증과 관련된 반복 자연유산에서 Methylenetetrahydrofolate Reductase돌연변이에 대한 분석 (The Analysis of Methylenetetrahydrofolate Reductase Mutation in Recurrent Spontaneous Abortion Associated with Hyperhomocysteinemia)

  • 남윤성;최종순;하권수;이지원;오도연
    • Clinical and Experimental Reproductive Medicine
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    • 제26권3호
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    • pp.441-445
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    • 1999
  • Objective: To analyze the methylenetetrahydrofolate reductase (MTHFR) mutation in recurrent spontaneous abortion associated with hyperhomocysteinemia. Material and Method: The blood sample of habitual aborter with high fasting homocysteine level was tested by PCR - RFLP method. Results: The patient was found to be a homozygosity for MTHFR gene mutation that was confirmed by the finding which is consistent with the mutation at the nucleotide 677 C to T, corresponding to Ala to Val. Conclusions: Hyperhomocysteinemia due to MTHFR mutation is a cause of recurrent spontaneous abortion. Therefore, the MTHFR mutation should be examined in the workup of recurrent spontaneous abortion showing hyperhomocysteinemia.

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반복자연유산에서 Methylenetetrahydrofolate Reductase 돌연변이에 대한 분석 (The Analysis of Methylenetetrahydrofolate Reductase Mutation in Recurrent Spontaneous Abortion)

  • 남윤성;차광렬;김남근;김선희;임진우;강금덕;강명서;김세현;오도연
    • Clinical and Experimental Reproductive Medicine
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    • 제28권3호
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    • pp.247-253
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    • 2001
  • Objective: To analyze the methylenetetrahydrofolate reductase (MTHFR) mutation in patients with recurrent spontaneous abortion. Material and Method: The blood samples of patients with recurrent spontaneous abortion were tested by PCR-RFLP method. Results: Of 51 cases of study group, 14 (27.5%) were normal, 25 (49.0%) were heterozygosity, and 12 (23.5%) were homozygosity. Of 58 cases of control group, 20 (34.5%) were normal, 30 (51.7%) were heterozygosity, and 8 (13.8%) were homozygosity. But the difference between two groups was not significant (p=0.190). Conclusion: Hyperhomocysteinemia due to MTHFR mutation is a cause of recurrent spontaneous abortion. Therefore, the study for MTHFR mutation should be included in the workup of recurrent spontaneous abortion.

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반복자연유산 환자에서 Homocysteine과 Methylenetetrahydrofolate Reductase 돌연변이의 상관관계에 대한 분석 (The Analysis of Interrelationship between Homocysteine and Methylenetetrahydrofolate Reductase Mutation in Patients with Recurrent Spontaneous Abortion)

  • 남윤성;차광렬;김남근;강명서;김세현;오도연
    • Clinical and Experimental Reproductive Medicine
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    • 제29권3호
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    • pp.187-193
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    • 2002
  • Objective : To analyze the interrelationship between homocysteine and methylenetetrahydrofolate reductase (MTHFR) mutation in patients with recurrent spontaneous abortion. Material and Method: Homocysteine and MTHFR mutation were tested by fluorescent polarizing immunoassay and PCR-RFLP method, respectively. Results: In patients with homocysteine level less than 5 ?mol/L, there was no case of normal group but there were four cases of heterozygosity and one case of homozygosity. In patients with homocysteine level 5$\sim$10 ? mol/L, the number of normal, heterozygosity and homozygosity group were eleven, eighteen and eight, respectively. In patients with homocysteine level $10{\sim}15$ ? mol/L, the number of normal, heterozygosity and homozygosity group were four, one and one, respectively. In patients with homocysteine level more than 15 ? mol/L, there was no case of normal and heterozygosity group but there were two cases of homozygosity. Conclusions: Hyperhomocysteinemia due to MTHFR mutation is a cause of recurrent spontaneous abortion. And there was a significant relationship between homocysteine and MTHFR mutation.

FLCN 유전자의 삼염기 결손 돌연변이를 동반한 일차성 자발성 기흉 1예 (A Case of Primary Spontaneous Pneumothorax with a Three Nucleotide Deletion Mutation of the FLCN Gene)

  • 박건;서홍주;장숙진;신봉석;홍란;이석기
    • Journal of Chest Surgery
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    • 제43권6호
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    • pp.824-828
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    • 2010
  • 일차성 자발성 기흉(primary spontaneous pneumothorax, PSP)의 원인은 명확하지 않다. 최근, FLCN 유전자의 돌연변이가 PSP의 한 원인인자으로 소개되고 있다. 반복적인 PSP를 주소로 한 47세 남성에서 고해상도 컴퓨터 단층 촬영 소견상 많은 폐기포와 다수의 큰 낭종과 함께 FLCN c.468_470 delTTC 돌연변이를 발견하여 문헌 고찰과 함께 보고하는 바이다.

No Effect of High Fat Diet-Induced Obesity on Spontaneous Reporter Gene Mutations in gpt Delta Mice

  • Takasu, Shinji;Ishii, Yuji;Matsushita, Kohei;Kuroda, Ken;Kijima, Aki;Kodama, Yukio;Ogawa, Kumiko;Umemura, Takashi
    • Asian Pacific Journal of Cancer Prevention
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    • 제15권17호
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    • pp.7149-7152
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    • 2014
  • A large number of epidemiological studies have demonstrated that obesity is a risk factor for several human cancers. Several animal studies using rodents with diet-induced or genetic obesity have also demonstrated that obesity can promote tumor development. However, the effects of obesity on the early stages of carcinogenesis, and especially on the spontaneous occurrence of somatic gene mutations, remain unclear. To investigate the effects of obesity on the rate of spontaneous gene mutations, we performed reporter gene mutation assays in liver, kidney, and colon, organs in which obesity appears to be associated with cancer development on the basis of epidemiological or animal studies, in mice with high fat diet (HFD)-induced obesity. Six-week-old male and female C57BL/6 gpt delta mice were fed HFD or standard diet (STD) for 13 or 26 weeks. At the end of the experiments, reporter gene mutation assays of liver, kidney, and colon were performed. Final body weights and serum leptin levels of male and female mice fed HFD for 13 or 26 weeks were significantly increased compared with corresponding STD-fed groups. Reporter gene mutation assays of liver, kidney, and colon revealed that there were no significant differences in gpt or $Spi^-$ mutant frequencies between STD- and HFD-fed mice in either the 13-week or 26-week groups. These results indicate that HFD treatment and consequent obesity does not appear to influence the spontaneous occurrence of somatic gene mutations.

Birt-Hogg-Dubé Syndrome Manifesting as Spontaneous Pneumothorax: A Novel Mutation of the Folliculin Gene

  • Kim, Kyung Soo;Choi, Hang Jun;Jang, Woori;Chae, Hyojin;Kim, Myungshin;Moon, Seok Whan
    • Journal of Chest Surgery
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    • 제50권5호
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    • pp.386-390
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    • 2017
  • $Birt-Hogg-Dub{\acute{e}}$ syndrome (BHDS) is a rare disease with autosomal dominant inheritance that manifests through skin tumors, pulmonary cystic lesions, and renal tumors. A mutation of FLCN located on chromosome 17p11.2, which encodes a tumor-suppressor protein (folliculin), is responsible for the development of BHDS. We report the case of a patient presenting with spontaneous pneumothorax, in whom a familial genetic study revealed a novel nonsense mutation: $p.(Arg379^*)$ in FLCN.

황색종 연초 돌연변이 계통 KF8832-85의 특성 (Characteristics of A New Flue-cured Tobacco Mutant Line KF 8832-85)

  • 조수헌
    • 한국연초학회지
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    • 제17권1호
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    • pp.27-32
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    • 1995
  • A new flue-cured tobacco mutant line BU 8832-85 was developed at Taegu Experiment Station, Korea Ginseng and Tobacco Research Institute in 1994. KF 8832-85 was resulted from a cross of flue-cured cultivars NC 95$\times$NC 2326, and developed by a pedigree system of breeding ; initial selection was made by plant type and resistance to bacterial wilt(BW) disease(heudomonas solanaceamm) in the F2 generation under the natural field conditions infested with the pathogen. One white flowered plant was occurred by spontaneous mutation in a certain line among the F3 generatioin while the others were pink. Six plants from the seeds by selfing were selected at the field infested with the pathogen among 240 populations with white flowering in the F4, KF 8832-85 was selected based on yield and leaf quality trials among 6 lines in Fs generation. BCF 8832-85 was compared with its Parent for certain agronomic and chemical characteristics at Taegu Experiment Station in 1993 and 1994. The results showed that KF 8832-85 have white flower, the stalk height was approximately that of NC 2326 but averaged about loom taller than NC 95. It produced ground suckers as much as NC 95, and did not breakdown leaf at the same as WC 2326. KF 8832-85 have high resistance to bacterial wilt disease. Yield of KF 8832-85 was 10 and 18% higher then that of NC 2326 and WC 95, respectively. Price per Kg was equal to that of NC 2326. The contents of nicotine and reducing sugar did not differ significantly from NC 95, while total nitrogen was significantly lower than NC 95. Therefore, the new mutant line is genetically stable for agronomic and chemical characteristics and provides a source of bacterial wilt disease resistance for use in breeding resistant flue-cured cultivars. Key words : Mutant line, White flower, Spontaneous mutation.

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개의 유선암종과 악성 비만세포 종양에서 발생한 종양억제 유전자 p53의 변이 (Mutation of Canine Tumor Suppressor Gene p53 in a Mammary Gland Adenocarcinoma and a Malignant Mast Cell Tumor)

  • Lee, Chung-ho;Kweon, Oh-kyeong
    • 한국임상수의학회지
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    • 제19권2호
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    • pp.195-198
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    • 2002
  • 개에서 자연적으로 발생한 12예의 종양에 대해, 종양 억제 유전자 p53의 변이와의 관계를 확인해 보았다. 종양조직에서 일반적인 방법으로 DNA를 추출하여, PCR 기법으로 p53을 증폭하여 염기서열을 확인한 결과, 개의 유선암종 예에서 exon 8의 codon 285에서 CCT $\longrightarrow$ TCT (proline $\longrightarrow$ serine)로 점변이 된 것이 확인되었다. 또한 악성 비만세포 종양 예에서도 exon 8의 codon 249에서 AGT $\longrightarrow$AGC로 점변이 된 것이 확인되었으나 silent point mutation (serine)으로 판명되었다. 이상의 결과를 토대로 개의 유선암종과 악성 비만세포 종양에서 종양억제 유전자 p53의 변이가 확인되었으며, 이는 종양의 형성과 관련된 p53의 역할이나 종양의 치료 및 예후 판정에 p53 을 활용하는 연구의 초석이 되리라 사료되며, 차후 이 유전자에 대한 광범위한 연구가 지속되어야 하리라 생각된다.

반수체 Saccharomyces diastaticus의 에탄올내성 증진 (Improvement of Ethanol-Tolerance of Haploid Saccharomyces diastaticus)

  • 송상호;김근;이민웅
    • 한국미생물·생명공학회지
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    • 제22권6호
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    • pp.584-592
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    • 1994
  • Several mutation procedures have been compared to obtain an ethanol-tolerant Saccha- romyces diastaticus strain secreting glucoamylase. These procedures include spontaneous mutation, EMS treatment, UV irradiation, and combination of EMS treatment and UV irradiation. All these methods were followed by adaptation of the yeast cells to gradually higher ethanol concentration. Among these procedures, the combined method of EMS treatment and UV irradiation gave the promising result, i.e. the ethanol tolerance of the yeast increased from 11.5%(v/v) to 14.0%(v/v). Respiratory deficient petite mutants of industrial and ethanol-tolerant yeast strains have been isola- ted and hybridized with haploid S. diastaticus strains. The resulting hybrids showed increased ethanol tolerance and starch-fermentability.

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폐 편평세포암에서 자발성 아포토시스와 원격전이 (Spontaneous Apoptosis and Metastasis in Squamous Cell Carcinoma of the Lung)

  • 오윤경;기근홍
    • Radiation Oncology Journal
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    • 제17권3호
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    • pp.203-208
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    • 1999
  • 목적 : 폐암 환자의 대부분은 진단 당시 수술을 받을 수 없는 병기로 발견되기 때문에 수술 조직이 아닌 기관지내시경 조직에서 자발성 아포토시스 정도를 평가하여 이의 임상적 의의에 대한 기초 자료로 삼고자 본 연구를 시행하였다. 대상 및 방법 : 1990년 9월부터 1994년 9월까지의 4년동안 흉부에 방사선치료를 받은 폐 편평세포암 환자 중 조직표본이 충분히 보관되어 있으며 추적이 가능하였던 19명을 대상으로 하였다. 병기는 II기가 1명, IIIa기 8명, IIIb기 5명, IV기 5명이었다. 면역조직화학적 염색법으로 자발성 아포토시스율(Al)과 p53 단백질 양성률을 관찰하였다. 결과 : 19명 중 16명은 $5\~15$ 개월 후에 사망하였으며 3명은 55, 67, 67 개월간 생존하고 있다. 중앙생존기간은 17개월, 평균 생존기간은 24 개월이었다. AI는 $0\~1\%$의 범위로 중앙값이 $0.4\%$였다. AI가 낮은 군에서 진단 당시 원격전이가 있었던 경우가 $50\%$ (5/10) 였고, 높은 근에서는 원격전이가 전혀 없었다(0/9). 생존기간에 영향을 줄 수 있는 예후인자들의 분석 결과 단변량 분석에서는 M병기가 통계학적으로 유의한 차이를 보였고, 다변량 분석에서는 AI, 화학요법, M병기, T병기, 병기가 의의가 있었다. 자발성 아포토시스와 p53 변이 사이의 관련은 관찰되지 않았다. 결론 : AI는 진단 당시 원격전이와 관련이 있으며, p53 변이와는 관련이 없었다. AI가 낮은 군에서 높은 군보다 생존기간이 짧은 경향을 보였다.

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