• 한국식품영양과학회지
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• 제19권4호
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• pp.335-341
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• 1990

Nuclei proteins were purified from chick liver to homogeneity by means of acid extraction CM Sephadex c 25 column chromatography and Bio Rex 70 column chromatography, The molecular weight of liver Nuclei proteins 1 and 2 as estimated by electrophoresis on SDS-polycrylamide gel are 29000 and 27,000 respectively. These molecular weights are identical with those of Nuclei Proteins 1 and 2 isolated from chick erythrocyte. The liver and erythrocyte Nuclei Proteins also co-migrated in acetic acid-urea gel electrophoresis. Furthermore the anti-sera raised against liver Nuclei Proteins 1 and 2 cross-reacted with erythrocyte Nuclei Proteins 1 and 2 respectively, However the amino acid compositions of liver Nuclei Prooteins 1 and 2 were found to be different from those of corresponding erythrocyte Nuclei proteins ; the contents of serine and proline in liver Nuclei proteins were higherocyte Nuclei proteins ; the contents of serine and proline in liver Nuclei protesins were higher than those in erythrocyte Nuclei proteins while the content of lycsine in liver Nuclei proteins was lower than the erythrocyte Nuclei proteins, These results suggest that in spite of similarities in many respects the liver and erythrocyte Nuclei proteins in chicks and different proteins.

• 한국미생물·생명공학회지
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• 제18권6호
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• pp.560-565
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• 1990

Trichocderma koningii의 영양요구성 돌연변이주인 CUT 121로부터 얻은 원형질체를 야생형인 ATCC 26113의 핵과 혼합하여 PEG 용액을 처리한 결과, 독립 영양형의 형질전환체가 30 이상의 빈도로 생성되었다. 이 독립영양형 군체로부터 얻은 분리체 중의 하나는 xylanase의 활성이 야생형보다 3배 가량 증진되었으며, 다른 세포의 다당류 분해효소는 야생형과 유사한 수준을 나타내었다. 분리체의 DNA 함량, 인위적인 불리양상 및 동위효소 양상 등을 조사 분석한 결과, 독립영양형의 형질전환체는 실험에 사용된 형질전환체로 판명되었다. 이상의 결과로 Trichoderma속 균류의 균주개량법으로, 핵전이법이 통상의 원형질체 융합법보다 효율적인 것으로 판명되었다.

• 정보처리학회논문지B
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• 제16B권2호
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• pp.131-140
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• 2009

본 논문에서는 입력된 FISH 세포영상을 군집세포영역과 독립세포영역으로 분류하고, 군집세포영역에 대해서는 하나의 세포를 분리하는 알고리즘을 제안한다. 먼저 입력된 영상에 대해서 가우시안혼합모델과 세포의 명암도 값에 대한 최대 우도 함수를 사용하여 세포영역과 배경영역을 분할해줄 임계값을 정의하게 된다. 이렇게 얻어진 전경세포영역에 대해서 보다 정확한 세포 분석을 위해서 군집세포와 독립세포를 분류하게 된다. 세포 영역의 분류과정을 위해서는 베이지안 네트워크와 확률밀도함수를 사용한다. 학습데이터로부터 밀집도(compactness), 평활도(smoothness), 후-모멘트(Hu-moment)에 대한 형태학적 특징값을 추출하여 확률밀도함수를 구성하고, 이를 기반으로 베이지안 네트워크를 사용하여 두 영역을 분류하게 된다. 군집세포로 분류된 영역에 대해서는 그 군집세포를 구성하고 있는 독립세포로 각각 분리한다. 먼저, 명암도 기울기 변환(intensity gradient transform) 영상과 워터쉐드 알고리즘을 이용하여 군집세포 영역을 작은 영역으로 분할하게 된다. 작게 분할된 영역을 하나의 세포영역으로 병합시키기 위해서, 군집세포에 존재하는 독립세포의 수만큼의 마커를 결정 침식 연산을 사용하여 추출하고, 추출된 마커를 중심으로 단계적 병합 알고리즘을 제안한다. 본 논문에서 제안한 방법은 166개의 FISH 세포를 사용하여 테스트한 결과 99.29%의 정확한 분리결과를 보여줬으며 기존의 다른 알고리즘보다도 뛰어난 성능과 빠른 실행시간을 보여주었다.

• Journal of Microbiology and Biotechnology
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• 제4권3호
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• pp.183-190
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• 1994

Cell-free extracts prepared from cultured insect cells, Spodoptera. frugiperda, were analyzed for activation of early gene transcription of an insect baculovirus, Autographa californica nuclear polyhedrosis virus (AcNPV). The template DNA used for in vitro transcription assays contained promoter sites for the baculovirus genes that have been classified as immediate early ($\alpha$) or early genes. These genes are located in the HindIII-K/Q region of the AcNPV genome. Nuclei isolated from the AcNPV-infected Spodoptera frugiperda cells were also used for in vitro transcription analysis by RNase-mapping the labeled RNA synthesized from in vitro run-on reaction in the isolated nuclei. The genes studied by this technique were p26 and pl0 genes which were classified as delayed early and late gene, respectively. We found that transcription of the genes from the HindIII-K region was accurately initiated and unique in the whole cell extract obtained from uninfected cells, although abundance of the in vitro transcripts was reverse to that of in vivo RNA. With isolated nuclei transcription of the p26 gene was inhibited by $\alpha$-amanitin suggesting that the p26 gene was transcribed by host RNA polymerase II. However, transcription of the pl0 gene in isolated nuclei was not inhibited by $\alpha$-amanitin, but rather stimulated by the inhibitor. We also found that the synthesis of $\alpha$-amanitin-resistant RNA polymerase was begun before 6 hr p.i., the time point at which the onset of viral DNA replication as well as the appearance of a-amanitin-resistant viral transcripts were detected. These studies give us strong evidence to support the previous data that early genes of AcNPV were transcribed by host RNA polymerease III, while transcription of late genes was mediated at least by a novel $\alpha$-amanitin-resistant RNA polymerase.

• Archives of Pharmacal Research
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• 제9권3호
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• pp.157-161
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• 1986

Isolated calf thymus nuclei were in vitro methylated with S- adenosy-L-methyl-$^{14}C$ methionine, and the proteins were fractionated according to their solubilities. Histone fraction ($H_{2}SO_{4}$-soluble fraction) contained approximately 60% total radioactivity incorporated, while "residual protein" which was ($H_{2}SO_{4}$-insoluble contained the remaining radio-activity. The "residual protein" was further fractionated into various acidic proteins, which contained very littel of the radioactivity. However, the protein fraction eluted from DEAE-cellulose with 0.5 N NaOH contained the largest amount of radioactivity. This protein was found to be basic in nature by amino analysis.

• 한국균학회지
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• 제16권4호
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• pp.210-213
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• 1988

맛느타리버섯(P. sapidus)의 균사체로부터 핵을 직접 분리하여 느타리버섯(P. ostreatus)의 원형질체에 전이시켜 다음과 같은 결과를 얻었다. 맛느타리버섯의 핵을 느타리버섯의 Arginine 영양요구성 균주 원형질체에 전이하여 얻은 균주의 균총 형태는 3종류로 구분되었으며, 형태 1은 균총이 두모균주의 모양으로 명확히 분리되었고, 형태 2는 균총은 분리되나 모균주와 다른 형태, 형태 3은 균총의 분리현상이 없이 안정하고 균일하게 생장하였다. 등전점 전기영동으로 핵 전이균주와 모균주의 Esterase, Malate dehydrogenase, Superoxide dismutase의 동질효소 pattern을 비교한 결과 핵 전이균주들은 모균주와 차이가 있었으며, 특히 형태 3의 두 균주는 모균주에서 볼 수 없는 새로운 band가 발견되었다.

• 생명과학회지
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• 제8권4호
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• pp.400-409
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• 1998

Formation of adduct was studied in benzo(a)pyrene(BP)- and doxorubicin(Dx)-treated human NC-37 cells and isolated nuclei. Major adducts formed were determined by fluorescence absorption spectrophotometery and DNA-lin-ked protein assay. When isolated nuclei were exposed to carcinogens BP and DMBA, and anticancer drugs m-AMSA, ellipticine and Dx, varying degrees of adduct formation occured between DNA-protein complex and these drugs. When the mixture was centrifuged 1.7 M sucrose solution, binding BP and DMBA appeared to be similar between the sediment and the supernatant. When the sediment was centrifuged again with 0.35% polymin-P, the amount of BP bound was 2-fold greater in the protein(1077$\pm$55cpm) than in DNA fraction (470$\pm$20cpm), whereas that of DMBA was 1.6-fold greater in the DNA than in protein fraction. In the case of m-AMSA, ellipticine and Dx, the amount of binding was slightly greater in supernatant than in sediment in centrifugation with 1.7 M sucrose, and more than 3 times greater in the DNA- than in protein- fraction in centrifugation with 0.35% polymin P. DNA fractions which associated with a subset of nonhistone chromosomal protein were isolated from NC-37 cells exposed to $^{3}$H-BP and $^{14}$C-Dx. They were separated into two distince components DNA-S and DNA-P by centrifugation with 2M Nacl chromatin extraction. The results indicated that the amount of $^{3}$H-BP bound was 6.0-fold greater in DNA-P as compared with DNA-S, while that of $^{14}$C-Dx binding appreaed to be 6.2-fold greater in DNA-S than in DNA-P fraction. When $^{3}$H-BP binding wasdetermined in the presence of cold Dx, the amount of binding was reduced only in the DNA-P fraction, indicating that the interaction between DNA and protein is decreased. Gene expression by these drugs, BP treated cells were increased to compare with nomal cells but reduced by treatment with BP-Dx. These results suggest that the protein moiety which tightly bound to DNA-P fraction may play an important role in the regulation of gene expression.

• 한국가축번식학회지
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• 제16권4호
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• pp.341-346
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• 1993

The development of isolated blastomeres from mammalian preimplantation embryos has been basically studied for the multiplication of embryos from superior animals. Therefore, this study was investigated the effect of co-culture with mouse fetal fibroblast cells(MFFC) on in vitro development of blastomeres from mouse preimplantation embryos. Mature female ICR mice were treated with hormone to induce superovulation and embryos were collected at each 2, 4, and 8-cell stage. Then, after removing zona pellucida with protease, blastomeres were isolated by micropipetting, or reconstituted with different stage blastomere, and incubated for 72 hrs either in T6 or TCM199 or on the monolayer of MFFC, which was prepared with fibroblast cells from 14∼14 day mouse fetus. After incubation, we examined their development rates every day and the nuclei numbers of each blastocyst by Hoechst-33342 staining. In the development rates of blastomeres, there were no significant differences between media but the higher rateswere found in the monolayer of MFFC, regardless of reconsititution. In addition, blastomeres cultured with MFFC had slightly greater number of nuclei than those cultured in single media. Generally, the higher development rates of blastomeres were found from earlier stage embryos than the later ones, regardless of culture conditions. Reconsitituted blastomeres had more nuclei but did not show the higher development rates, compared to the single blastomeres. Taken together, our results suggest that co-culture with MFFC have a beneficial effect on the in vitro development of blastomeres from mouse embryos.

• Journal of Microbiology and Biotechnology
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• 제7권3호
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• pp.161-166
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• 1997

Nuclei were isolated from the protoplasts of Trichoderma harzianum T95 and treated with colchicine, a polyploid inducer. The nuclei were transferred into the protoplast of multi-auxotrophic Gliocladium virens G88 which cannot grow in minimal medium. The protoplast of G. virens G88 carrying the transferred nuclei were regenerated in a regeneration minimal medium containing $17{\mu}g/ml$ of chloroneb as a haploid inducer. Six intergeneric hybrids between G. virens and T. harzianum were isolated from the regeneration minimal medium. The hybrids could be classified into three types according to morphology, those with an isozyme pattern, those with an protein band and those with an randomly amplified polymorphic DNA(RAPD) pattern produced by random primers and repetitive sequences. The first group was identified to be a haploid recombinant, the second group a heterokaryon, and the third appeared to be petite.

• 한국균학회지
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• 제15권4호
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• pp.250-253
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• 1987

원형질체내에 외래유전물질 도입에 의한 균주 개발의 가능성 검토의 일환으로 사철느타리의 원형질체로부터 핵을 분리하여 느타리의 원형질체내로 전이하여 얻은 결과는 다음과 같았다. 1. 핵전이주는 크게 3가지 type으로 구분되었는데 type 1은 아주 빠른 균사생장과 clamp connection를 형성하지 않으며 CM+benomyl에서 균총분리가 나타남으로서 이질이배체로 사료되었다. type 2는 주된 핵전이주로서 모균주와 비슷하거나 다소 빠른 균사생장과 clamp connection을 지녀 자실체를 형성하였으며 heterokaryon으로서 원형질체 융합주와 유사하였다. 그러고 type 3은 핵 또는 염색체 단편의 전이로 clamp connection를 지니지 않고 아주 느리거나 MM에서 생육이 거의 불가능한 균주였다. 2. 핵전이주 및 모균주를 전기영동법으로 esterase 동위효소 pattern을 조사한 결과 핵전이주는 모균주와 구별되었는데 type 1인 이질이배체는 새로운 band를 나타내었으며, type 2와 type 3은 모균주들을 합한 것으로 보였다.