• 제목/요약/키워드: Chromosomes 2

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배양한 子宮癌세포의 염색체에 관한 연구 (Chromosome Studies on the Cultured Uterine Carcinoma Cells)

  • 강영선;김석환;이정길
    • 한국동물학회지
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    • 제13권1호
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    • pp.29-33
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    • 1970
  • 한국부인의 子宮癌細胞에 관한 본 연구결과는 다음과 같다. 1. 種族細胞의 染色體數는 45와 46의 2종류임을 확인했다. 2. 染色體 형태에 있어서 diplochromosome 의 출현율이 높아 5.3%을 나타낸다. 染色體 異常率은 細胞당 0.16이고, 異常型으로는 染色分體缺矢, 同位染色分體缺矢의 染色分體異常型과 2動原體인 染色體異常型이 보였다. 3. 核型을 분석한 결과 전체로는 그르프 F의 染色體數의 증가와 그르프 B 및 E의 감소경향을 보여주었다. 이것이 低2倍性인 細胞에서는 그르프C 및 G에서 감소하고, 반대로 高2倍性에서는 그르프C 및 G에서 증가하는 경향이 있었다.

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한국산 동사리과 (Odontobutidae)와 둑중개과 (Cottidae) 5종의 핵형 (Karyotypes of Five species in Odontobutidae and Cottidae of Korea)

  • 박갑만;송호복
    • 한국어류학회지
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    • 제18권3호
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    • pp.155-162
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    • 2006
  • 한국산 동사리과 (Odontobutidae)의 동사리 (Odontobutis platycephala), 얼록동사리 (O. interrupta), 남방동사리 (O. obscura) 그리고 둑중개과 (Cottidae)의 둑중개 (Cottus koreanus), 한둑중개 (C. hangiongensis) 등 5종의 핵형 분석을 실시하였다. 동사리, 얼록동사리, 남방동사리의 염색체 수 및 핵형은 2n=44 (22T), NF=44였으며, 둑중개와 한둑중개의 염색체 수와 핵형은 2n=48(2ST+22T), NF=52로 밝혀졌다.

한국산 석패와 7종의 염색체 연구 (Chromosomal Study of Seven Species of Unionidae ( Bivalvia : Palaeoheterodonta ) in Korea)

  • 박갑만;권오길
    • 한국패류학회지
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    • 제7권1호
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    • pp.12-29
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    • 1991
  • The chromosome numbers and the karyotypes of seven species in Unionidae are reported, using air drying in gonad. In seven species, the chromosome number of 38(2n) was counted. The mitotic chormosomes of A. arcaeformis flavotincta, A. woodiana and L. gottschei hd 7 pairs of metacentric and 12 pairs of submetacenrtic chromosomes, U. douglasiae had 6 pairs of metacentrics, 13 pairs of submetacentrics, U. douglasiae sinuolatus had 4 metacentric pairs and 15 submetacentric pairs, L. acrorhyncha had 5 metacentric pairs and 14 submetaacentric pairs, and S. triangularis had 5 mdtacenrtric pairs, 13 submetacentric pairs and 1 pair of subtelocentric chromosomes. The size of chromosomes of A. woodiana was the longest in length and L. gottschei was the shortest. The sexual difference of chromosomes was not observed.

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지식 베이스를 이용한 교육용 염색체 분석 시스템 (Chromosome Analysis System based on Knowledge Base for CAI)

  • 박정선;신용원
    • 한국지능정보시스템학회:학술대회논문집
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    • 한국지능정보시스템학회 2001년도 춘계정기학술대회
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    • pp.215-222
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    • 2001
  • The task for chromosome analysis and diagnosis by experienced cytogenetists are being concerned as repetitive, time consuming job and expensive. FOr that reason, chromosome analysis system based on knowledge base for CAI had been established to be able to analyze chromosomes and obtain necessary advises from the knowledge base instead of human experts. That s to say, knowledge base by IF THEN production rule was implemented to a knowledge domain with normal and abnormal chromosomes, and then the inference results by knowledge base could enter the inference data into the database. Experimental data were composed of normal chromosome of 2,736 patients'cases and abnormal chromosomes of 259 patients'cases that have been obtained from GTG-banding metaphase peripheral blood and amniotic fluid samples. The complete system provides variously morphological information by analysis of normal or abnormal chromosomes and it also has the advantage of being able to consult with user on chromosome analysis and diagnosis.

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단관백색레그혼순계에 있어 중심입지수, 등완비 및 상대적길이에 의한 염색체의 형태적 특징과 수에 관한 연구 (Study on the Chromosome Size, Number and Shape by the Centromeric Index, Arm Ratio and Relative Length in Single Comb White Leghorns)

  • 오봉국;손시환;최연호
    • 한국가금학회지
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    • 제13권2호
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    • pp.167-172
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    • 1986
  • 본 연구는 단관백백레그혼순계 염색체의 형태적 특징과 크기를 명확히 구명하기 위하여 중심입지수, 등 완비 및 상대적 길이를 측정하여 이용하고 이들의 염색체 수를 밝혔다. 시험재료로서는 서울대학교 부속목장에서 사육중인 단관백색레그혼순계 암컷 20수와 수컷 5수를 공시하고 이들을 수정시켜 50개의 수정란에 대하여 염색체 분석을 하였다. 분석방법으로서는 중기상의 포착을 위하여 colchicine을 이용하고, hypotonic, fixation, air-drying 처리를 하여 나타난 초기 metaphase상으로서 핵형분석하였다. 시험 결과 분석된 각 염색체의 형태적 특징은 다음과 같다. 1. 1,2심 염색체 : meta 및 submetacentric으로서 이들 둘 간에는 크기에 따라 명확히 구분된다. 2. 3,4심 염색체 : 길이는 서로 비슷하나, 4심 염색체에서는 짧은 단완이 나타나고, 3심은 acrocentric 형태이다. 3. 5심 염색체 : 성염색체(Z)로서 metacentric 형태이다. W 염색체 역시 metacentric 이지만 7-8심 염색체 크기 정도이다. 4. 6심 염색체 : 3심과 같이 acro 형체이나 3심 염색체 크기의 반정도이다. 5. 7,8심 염색체 : 6심 크기의 반정도로서 길이는 서로 비슷하나 7심은 짧은 단완을 가지고, 8심은 acrocentric 염색체이다. 6. 9심 염색체 : 7심과 8심의 크기와 비슷하나 metacentric 양상이다. 7. 나머지 30쌍의 소형염색체 : 점의 형태로서 대부분 acrocentric 형태이다. 이 밖에도 염색체의 수에 있어서 관찰된 sample의 58%가 78개로 나타났고, 나머지는 72-77개로 나타남에 따라 이의 염색체 수는 최소 78개로 사료된다.

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한국산 Paramphistomum explanatum(Creplin, 1849)의 핵형분석 (The Karyotype of Payamphistomum explanatum(Creplin, 1849) Obtained from Korean Cattle)

  • 이재구;강창원;이호일
    • Parasites, Hosts and Diseases
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    • 제24권1호
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    • pp.42-48
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    • 1986
  • As a series of systematic classification of paramphistomes, in the first step, paramphistomes in the lumen and reticulum were collected on 170 Korean catties (2∼3 years age, male) slaughtered at Jeonju abattoir from July, 1984 to September, 1985 and were classified by means of morphology of the worms. Afterwards, the karyotype of Paramphistomum explanatum (Creplin, 1849) which is the common in Korean cattle was detected by means of modified air-drying method from testis cells of the worm. The following is a brief summary of the leading facts gained through the experiment. 1. Most of the cattle slaughtered at the abattoir were infected with paramphistomes. The 5 species of the worms were detected on 170 Korean cattle and the worm burden per head was from 2 to 784(on the average 170) worms, 120(70.59%) heads out of them involving 2∼100 worms. In 28,900 individuals of paramphistomes obtained on 170 Korean cattle, appearance rates of various worms were as follows : 49.74% in P. explanatum, 48.08% in P. cervi, 0.98% in Orthocoelium orthocoelium, 0.89% in Fischoederius cobboldi and 0.14% in Cotylophoron cotylcphorum. 2. The chromosome number of 620 P. explanatum in the haploid and diploid cells was n=9 and 2n=18, and abundant cells in meiotic division were observed; 1,420 haploid and 38 diploid cells were reliable. Nine pairs of mitotic chromosomes were homologous and the chromosomes were composed of aye medium-sized metacentrics(m), subtelocentrics(st) or submetacentrics(sm) and four smallsized subtelocentrics(st) or submetacentrics(am), while meiotic metaphase chromosomes were composed of five medium and four small-sized. 3. The haploid of the testis cells showed C-band in the centromeric region from 8 of them, whereas the remaining chromosome No. 5 included heterochromatin on the tip region, and chromosomes No. 3 and No. 7 showed a remarkable C-band distinguished from other chromosomes.

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오골계의 염색체 분염법 (G-banding)에 따른 핵형분석에 관한 연구 (The Study of G- Banding Chromosome in Silkie)

  • 강태석;오봉국;손시환
    • 한국가금학회지
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    • 제12권2호
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    • pp.83-87
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    • 1985
  • This experiment was carried out to identify the chromosomes of silkie. It was many difference from other breeds in morphology and characteristics. In this experiment, chromosomal analysis was used early embryos. In aspect of morphological chromosomes, chromosomal size and shape are similar to other breeds. The chromosomes of silkie were shown to morphlogy as follows. They were identified that chromosome #l and #2 were grouped as submentacentric, #3, #5 and #6 were telocentric #4 and #7 were acrocentric and #8 was metacentric chromosome. Zㆍsex chromosome was shown 5th, W-sex chromosome was 8th to 9th and they were metacentric chromosome, respectively. Each chromosome through the G-banding was shown the 3 dark bands in 1 p2, distinct light band in 1p1, dark band in 2p2, broad light band in 3pl, dark band from centromere and distal part in 4th chromosome and dark band in 5pl. Z-sex chromosome was shown dark at p-arm distal part.

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New Zealand White 토끼의 생식세포 및 체세포 분열에 의한 염색체 분석 (Chromosomal Analysis of Meiosis and Mitosis in New Zealane White Rabbit)

  • 신선희;김희수;최영현;이원호
    • 생명과학회지
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    • 제11권4호
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    • pp.354-361
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    • 2001
  • Chromosomal characteristics of New Zealane White rabbit was studied at meiosis and mitosis. The meiotic chromosomal preparations were mad with the modified air-drying method and karyotype analysis was performed with the G-banding technique, using isolated mitotic metapase chromosomes of the New Zealand White rabbit. Chromosomes, sex vesicles and centromeres could be classified in the zygotene and the pachytene of the meiosis I. The hair-like processes projecting laterally from the axes of bivalent chromosomes at the mid-to-late pachytene were observed and made the appearance of the lampbrush chromosome structure. Chromosomes could be classified onthe basis of the numbers and locations of chiasma in the diakinesis. Twenty-one autosomal bivalents and a single unequal terminally associated X-Y bivalent were observe during the late prophase and the metaphase of the meiosis I. Most of the bivalent types observed in the New Zealand White rabbit spermatrocytes were 1CH, 1TAl, and 2TA bivalents. The mean chiasma frequency(CF) of the male New Zealand White rabbit was 30.2 and it was found that the CF value tended to decrease through diakinesis and the metaphase I. The karyotype of the New Zealand White rabbit was a male chromosome number of 44(2n=44) comprising 8 pairs of metacentric, 9 pairs of submetacentric, 4 pairs o acrocentric autosomes, metacentric X chromosome and acrocentric Y chromosome.

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Creation of an Ethanol-Tolerant Yeast Strain by Genome Reconstruction Based on Chromosome Splitting Technology

  • Park, A-Hwang;Sugiyama, Minetaka;Harashima, Satoshi;Kim, Yeon-Hee
    • Journal of Microbiology and Biotechnology
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    • 제22권2호
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    • pp.184-189
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    • 2012
  • We sought to breed an industrially useful yeast strain, specifically an ethanol-tolerant yeast strain that would be optimal for ethanol production, using a novel breeding method, called genome reconstruction, based on chromosome splitting technology. To induce genome reconstruction, Saccharomyces cerevisiae strain SH6310, which contains 31 chromosomes including 12 artificial mini-chromosomes, was continuously cultivated in YPD medium containing 6% to 10% ethanol for 33 days. The 12 mini-chromosomes can be randomly or specifically lost because they do not contain any genes that are essential under high-level ethanol conditions. The strains selected by inducing genome reconstruction grew about ten times more than SH6310 in 8% ethanol. To determine the effect of mini-chromosome loss on the ethanol tolerance phenotype, PCR and Southern hybridization were performed to detect the remaining mini-chromosomes. These analyses revealed the loss of mini-chromosomes no. 11 and no. 12. Mini-chromosome no. 11 contains ten genes (YKL225W, PAU16, YKL223W, YKL222C, MCH2, FRE2, COS9, SRY1, JEN1, URA1) and no. 12 contains fifteen genes (YHL050C, YKL050W-A, YHL049C, YHL048C-A, COS8, YHLComega1, ARN2, YHL046W-A, PAU13, YHL045W, YHL044W, ECM34, YHL042W, YHL041W, ARN1). We assumed that the loss of these genes resulted in the ethanol-tolerant phenotype and expect that this genome reconstruction method will be a feasible new alternative for strain improvement.

종양세포(腫瘍細胞)의 염색체(染色體)에 대한 오크라톡신 A의 독성(毒性)에 관한 연구(硏究) (Studies on toxicity of ochratoxin A to chromosomes of turmor cell-line)

  • 윤화중;노민희;김강련
    • 대한수의학회지
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    • 제29권2호
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    • pp.51-57
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    • 1989
  • This study was performed to investigate the toxicity of ochratoxin A (OA) to the chromosomes of $K_{562}$ tumor cell-line in vitro. The results of this experiment were as follows: 1) Chromosomes of $K_{562}$tumor cell-line resulted in pseudotriploidy on the control group. Chromosomes of $K_{562}$ tumor cell-line treated with OA resulted in heteroploidy compared with the control group. The mean number of chromosomes in the karyotype of the control group (60) were 7 in the A group, 5 in the B group, 20 in the C+X group, 7 in the D group, 9 in the E group, 6 in the F group, and 6 in the G+Y group respectively. The number of chromosomes were increased as follows: Treating with $0.7{\mu}M$ OA, the number of chromosomes were increased one in E and F group, two in G+Y group compared with control group. In treated with $1.5{\mu}M$ OA, the increasing number of chromosome was one in E and F group. In treated with $3{\mu}M$ OA, E and F group was increased one and G+Y group were increased two chromosomes compared with control group. But in treated with $6{\mu}M$ OA, the number of chromosome in G+Y group was decreased one. 2) $K_{562}$ tumor cell line treated with OA showed Philadelphia-Chromosome in the long arm of the G group karyotype chromosome. The rate of chromosome aberration in $K_{562}$ tumor cell-line treated with OA was 77% in $0.7{\mu}M$ OA group, 71% in $1.5{\mu}M$ OA group, 82% in $3{\mu}M$ OA group and 94% in $6{\mu}M$ OA group respectively. The rate of chromosome aberration of $K_{562}$ tumor cell-line treated with OA was high in the high dose level of OA, and chromosome aberration of $K_{562}$ tumor cell-line treated with OA showed deletion, minute, dicentric-chromosome and translocation in the long arm of the C-group karyotype. As a result of this study, the toxicity of OA showed deletion, minute, dicentric-chromosome and translocation in the long arm of the C-group karyotype, and then, the toxicity of OA resulted in the damage to RNA and protein synthesis in $K_{562}$ tumor cell-line, and the C-group karyotype of $K_{562}$ tumor cell-line was target of the toxicity of OA.

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