• Title/Summary/Keyword: 배아체

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Endoplasmic Reticulum and Protein Body Formation in Developing Endosperm Cells of Ginseng Seed (발달중인 인삼(Panax ginseng) 종자 배아세포의 소포체 및 단백과립 형성)

  • Yu, Seong-Cheol;Chae, Eun-Ju;Kim, U-Gap
    • Journal of Ginseng Research
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    • v.15 no.2
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    • pp.131-138
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    • 1991
  • This study was carried out to investigate the development of endoplasmic reticulum and the formation of Protein body in the endosperm cell during seed formation of Panax ginseng C. A. Meyer with electron microscope. In the endosperm cell of early developmental process after pollination, vesicles that contain storage materials produced in rough endoplasmic reticulum incorporated into central vacuole. The central vacuole is gradually subdivided into several small-sized vacuoles and increased in number. Amorphous proteinaceous materials of high electron density are produced in rough endoplasmic reticulum. Rough endoplasmic reticulum increase in number and surround the protein body and vesicles circularly. Spherical proteinaceous granules with limited membrane appeared from the amorphous granules at the peripheral region of the rough endoplasmic reticulum. Gradually, storage materials are accumulated within the vacuole surrounded by spherosomes. Protein bodies are formed by interfusing between vacuoles and vesicles derived from rough endoplasmic reticulum which contained the amorphous protein of high electron density.

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Development of Expressed Sequence Tags(ESTs) from Korean Native Chicken cDNA Libraries

  • Shin, Sang-Su;Song, Ki-Duk;Shin, Jee-Hye;Lee, Sun-Duck;Lee, Young-Mok;Kim, Jin-Kyu;Han, Jae-Yong
    • Proceedings of the Korea Society of Poultry Science Conference
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    • 2003.11a
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    • pp.67-68
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    • 2003
  • 한국 재래 닭의 유전적 특성 규명 및 기능 유전체 연구의 기초재료를 확보하고자 대량 EST 염기서열 결정 및 생물정보학 분석을 실시하였다. 대량 EST 염기서열 분석을 위한 첫 번째 단계로 재래 닭의 뇌, 비장, 정소, 배아 생식기를 이용하여 cDNA library를 구축하였다. 각각의 library로부터 총 15,121개의 클론을 선정하여 염기서열을 결정하였다. 생물정보학 분석결과 15,121개의 염기서열은 총 10,353개의 contig로 정리되었다. 이들 염기서열을 기존 데이터베이스를 대상으로 tBlastX(http://www.ncbi.nlm.nih.gov/BLAST) 분석을 실시한 결과, 염기서열 중 56 %가 기존 데이터베이스에 존재하는 유전자와의 상동성을 보였다. 상동성을 보이는 유전자들은 유전자의 구조 및 기능 분석에 이용될 것이고, 상동성을 보이지 않는 유전자들은 microarray와 같은 대량 유전자 발현분석 시스템을 이용하여 선별한 후 기능분석이 실시될 것이다.

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Aesthetic Study of Film Sound in Godard's (고다르 <카르멘이라는 이름(Prénom Carmen)>에 나타난 영화 사운드의 미학적 고찰)

  • Park, Byung-Kyu
    • The Journal of the Korea Contents Association
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    • v.18 no.8
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    • pp.82-91
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    • 2018
  • This paper examines the sound of Godard's <$Pr{\acute{e}}nom$ Carmen> from Deleuze's film aesthetics and Merleau-Ponty's phenomenological point of view. The rehearsal scene of a string quartet is a mirror-image that illuminates the music itself, and becomes a crystal-image with the indiscernibility of the present and the past in the break with the main narrative. On the other hand, urban noise and waves are the seeds composed of pure optical (sound) images and grow into pure sound crystals that collide with what is seen through the juxtaposition, substitution, and intentional connection of sound. However, these sound contradictions also lead to the integrated sound category as a 'sole movement' through Merleau-Ponty's dialectical thought, and even the dialectical sound management of pop and classical music is no longer a confrontation of the genre, but is integrated into the materialistic category of sound. This study is differentiated from the existing research by solving the sound aesthetics of the Godard's film through philosophical thought.

Expression of ADAM-8, 9, 10, 12, 15, 17 and ADAMTS-1 Genes in Mouse Uterus During Periimplantation Period (착상 전후시기의 생쥐 자궁조직에서의 ADAM-8, 9, 10, 12, 15, 17과 ADAMTS-1 유전자의 발현)

  • Kim, Ji Young;Koog, Min Ji;Bae, In Hee;Kim, Haekwon
    • Clinical and Experimental Reproductive Medicine
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    • v.32 no.1
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    • pp.33-46
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    • 2005
  • 연구목적: ADAMs은 metalloprotease/disintegrin domain을 가진 transmemebrane glycoprotein으로써 지금까지 30개 이상의 ADAM 및 10개 이상의 ADAMTS가 알려져 있다. 이들의 기능은 포유동물의 수정 시 sperm-egg binding과 fusion, myoblast fusion, integrin과의 결합 등에 직접 관여하거나, TNF-alpha 등의 생체신호전달물질이 세포로부터 분비될 때에 이들의 구조를 변화시켜 활성화시키는 효소작용, 그리고 dendritic cell differentiation 등에 관여하는 것으로 알려져 있다. 그러나 자궁내막 조직에서의 유전자 및 단백질 발현 여부에 관해서는 거의 보고되어 있지 않고 있다. 본 연구에서는 착상 전후 시기의 생쥐 자궁조직에서 ADAM-8, 9, 10, 12, 15, 17 그리고 ADAMTS-1의 유전자가 발현하는 지를 알아보았다. 연구 재료 및 방법: 본 연구에서는 생쥐의 자궁조직을 대상으로 ADAM-8, 9, 10, 12, 15, 17 그리고 ADAMTS-1을 선정하여, 초기 임신 기간에서의 유전자 발현 여부를 조사하였고 이 결과를 바탕으로 자궁조직에서의 이들 유전자들의 생리적인 기능을 규명하고자 하였다. 결 과: 임신한 생쥐 자궁조직에서의 ADAM-8, 9, 10, 12, 15, 17 그리고 ADAMTS-1의 유전자 및 단백질의 발현 양상을 RT-PCR 방법을 이용하여 알아본 결과, 조사된 ADAM 종류와 임신 날짜별로 다르게 나타났다. ADAM-8의 유전자 전사체는 임신 1일째 매우 강하게 발현되었으나 임신 3일째로 진행되면서 감소하다가 이후 다시 임신 5일째가 되면서 증가하는 양상을 보였다. ADAM-9, 10, 17 그리고 ADAMTS-1의 경우는 임신 1일째에서 5일째까지 유전자의 발현 양상이 크게 변하지 않았고 ADAM-12와 ADAM-15의 유전자 전사체는 임신 1일에서 5일로 진행되면서 현저하게 증가되는 양상을 보였다. 이후 임신 6일에서 8일에서는 생쥐 배아가 착상된 부위와 비 착상부위로 나누어 유전자의 발현 양상을 관찰한 결과, 조사된 ADAM 모두 비착상 부위보다 착상부위에서 유전자 전사체의 발현이 크게 증가되는 것으로 나타났다. 결 론: 이상의 결과로 미루어 ADAM 유전자는 임신초기 착상과정과 임신 단계에 따른 자궁의 조직 재구성에 중요한 역할을 할 것으로 생각된다.

Genetic Polymorphism of Avian Leukosis Virus Host Receptors in Korean Native Chickens and Establishment of Resistant Line

  • Lee, Kyung Youn;Shin, Yun Ji;Han, Jae Young
    • Korean Journal of Poultry Science
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    • v.49 no.2
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    • pp.99-108
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    • 2022
  • Avian leukosis virus (ALV) is a highly contagious retrovirus that causes tumors and has resulted in great economic loss worldwide owing to its high transmission rate. Various ALV viral subgroups exist, with infections occurring via specific host receptors. The susceptibility or resistance of avian species to the ALV-A and K subgroups is determined by the host receptor, the tumor virus locus A (tva) gene, while that to ALV-B depends on another host receptor, the tumor virus locus B (tvb) gene. The resistance alleles of tva and tvb have primarily been identified in China, but none have beendetected in Korea. We analyzed the frequencies of tva and tvb genotypes in White Leghorn (WL), Korean Ogye (KO), and Korean native chicken (KNC) breeds, and assessed the resistance to ALV subgroups. In WL, both tva and tvb had various genotypes, including susceptibility and resistance alleles, whereas in KO, tva and tvb resistance alleles were dominant. In KNC, tva susceptibility and resistance alleles were mixed, whereas tvb resistance alleles were dominant. In addition, we showed that there were differences in the splicing pattern of tva transcripts and the expression level of tvb transcripts within breeds. Finally, we confirmed that ALV resistance depended on KO and KNC genotypes by in vitro infection of chicken embryonic fibroblasts with ALV. These results highlight that some KO and KNC individuals are naturally resistant to ALV subgroups A, B, and K, and will facilitate the preservation of economically superior traits through selective breeding.

The Effect of Estrogen on the Transcription of the Insulin-like Growth Factor-I Gene in the Uterus (자궁 내 insulin-like growth factor-I 유전자 발현에 미치는 에스트로겐의 영향)

  • Kwak, In-Seok
    • Journal of Life Science
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    • v.19 no.5
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    • pp.593-597
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    • 2009
  • The uterus plays a critical role in pregnancy and steroid hormones, and both estrogen (E2) and progesterone (P4) especially play important roles in the cross-talk between embryos and uterus to support the pregnancy. E2 stimulates uterine growth during early pregnancy to prepare for implantation of embryos. This cross-talk during the implantation period involves hormones (E2 and P4) and growth factors, including insulin-like growth factor-I (IGF-I). In the uterus of a pregnant pig, the action of E2 is mediated by estrogen receptor-${\beta}$ (ER-${\beta}$). The expression of ER-a was much higher in early pregnancy than in mid- and late- pregnancy, suggesting E2 secretion from embryos enhances transcription of ER-a during early pregnancy. In order to prove whether IGF-I is an E2 target gene, quantitative real-time PCR was performed on ovariectomized murine uterus with E2 and/or P4 treatment(s). Increased IGF-I mRNA expression was observed with E2 treatment, however, it was not significantly induced by P4 treatment, which clearly demonstrates that, in mice, E2 depends on the activation of uterine IGF-I gene expression. The expression of IGF-I in the uterus of pigs was much higher in early pregnancy than in mid- and late- pregnancy and these data exhibited the same expression pattern with the ER-${\beta}$ gene expression in the uterus. It suggests that a positive co-relationship between IGF-I and ER-${\beta}$ expression exists in the uterus, and that both gene expressions of IGF-I and ER-${\beta}$ are regulated by E2. It further suggests that uterine the IGF-I gene expression might be initiated by E2 secreted from embryos to increase ER-${\beta}$ gene expression, and that this increased ER-${\beta}$ further stimulates the expression of IGF-I in the uterus during early pregnancy.

A Current Advance of Gene Targeting and Gene Trapping Methods As Tools of Making Transgenic Mice (형질전환생쥐의 제조 수단으로서 유전자 적중법 및 함정법의 개발 현황)

  • Kang, Hae-Mook
    • Development and Reproduction
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    • v.14 no.4
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    • pp.215-223
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    • 2010
  • The construction of transgenic mouse using embryonic stem (ES) cells has been crucial in the functional studies of gene on mouse genome. Gene knockout mice have been powerful for elucidating the function of genes as well as a research model for human diseases. Gene targeting and gene trapping mathods have been the representative technologies for making the knockout mice by using ES cells. Since the gene targeting and the gene trapping methods were independently developed about 20 years ago, it's efficiency and productivity has been improved with a advance of molecular biology. Conventional gene targeting method has been changes to high throughput conditional gene targeting. The combination of the advantage of gene targeting and gene tapping elements allows to extend a spectrum of gene trapping and to improve the efficiency of gene targeting. These advance should be able to produce the mutant with various phenotype to target a certain gene, and in postgenome era they have served as crucial research tools in understanding the functional study of whole genome in mouse.

Expression of OB-R, Regulation of Mitogen Activated Protein Kinase Activity and Maturation by Leptin in Mouse Oocytes (생쥐 난자 및 초기배아에서 Leptin 수용체 발현 및 Leptin에 의한 Mitogen Activated protein Kinase 활성의 조절 및 난자의 성숙 조절)

  • Kang, Byung-Moon;Han, Hyun-Joo;Seo, Hye-Young;Hong, Suk-Ho;Gye, Myung-Chan
    • Clinical and Experimental Reproductive Medicine
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    • v.28 no.2
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    • pp.111-120
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    • 2001
  • Objective: To verify the expression of leptin receptor (OB-R) in oocytes and preimplantation embryos, the involvement of mitogen activated protein kinase (MAPK or Erk1/2) in the leptin signaling, and effect of leptin on the oocyte maturation in mice. Method: RT-PCR analysis of OB-R was conducted in germinal vesicle (GV)-intact and MII stage oocytes, and 1, 2, 8-cell embryos and blastocysts. Germinal vesicle breakdown (GVB), polar body extrusion, monitored in the presence or absence of leptin ($1{\mu}M$). Following the leptin treatment, temporal changes in MAPK activity were verified by immunoprecipitation and in vitro kinase assay in MII oocytes. Results: The expression of OB-R mRNA was found in GV and MII oocyte but not in the embryos. MAPK activity of the MII oocytes was significantly increased by brief incubation in the HTF supplemented with leptin ($1{\mu}M$). Priming of PD098059, a MEK inhibitor to leptin treatment attenuated the activation of MAPK by leptin in MII oocytes. Following 24 hrs of culture of the GV oocytes, leptin significant increased the GVB and 1 st polar body extrusion. Conclusion: This result suggested that functional interaction between leptin and OB-R resulted in potentiation of MAPK (Erk1/2) activity in MII oocytes through MEK activation and that leptin might be a local regulator of meiotic maturation of the mouse oocytes.

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STUDIES ON THE LEVELS OF INDOLE-3-ACETIC ACID (IAA) AND INDOLE-3-ACETYL-L-ASPARATE(IAAsp)IN RELATION TO SOMATIC EMBRYOGENESIS OF CALLI DERIVED FROM GINSENG (PANAX GINSENG C.A. MEYER) ROOTS (인삼근 캘루스의 체세포 배아 발생과 관련한 IAA 및 IAAsp의 수준에 관한 연구)

  • Chen Kai-hsien;Hsing Yue-ie;Chen Shuh-chun;Chang Wei-chin
    • Proceedings of the Ginseng society Conference
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    • 1984.09a
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    • pp.45-48
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    • 1984
  • Ion-pair reverse phase HPLC techniques were used to compare the contents of IAA and IAAsp in the embryogenic and non-embryogenic calli derived from ginseng (Panax ginseng C.A. Meyer) root tissues. The contents of IAA and IAAsp of the embryogenic callus were much higher (7 to 18 X respectively) than those of non-embryogenic callus. There is a distinct fluorescent peak of an unknown component in the HPLC profile of the extract for indolic compounds from non-embryo-genic callus. This distinct difference may be employed as a promising parameter to screen the culture pieces for obtaining the calli with high potential for embryoid formation.

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Stem Cell Based Strategies for the Treatment of Degenerative Retinal Diseases (망막변성질환에서의 줄기세포 기반치료)

  • Park, Jung-Hyun;Ku, Seung-Yup;Cho, Myung-Soo;Lee, Hak-Sup;Choi, Young-Min;Moon, Shin-Yong;Yu, Hyeong-Gon
    • Clinical and Experimental Reproductive Medicine
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    • v.37 no.3
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    • pp.199-206
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    • 2010
  • Stem-cell therapy has the potential to improve vision in patients with untreatable retinal disease. Various types of cell source including fetal, embryonic and adult stem cells, intrinsic and extrinsic factors for differentiation into retinal progenitors and transplantation mode were discussed in this review. Experimental approaches have successfully induced photoreceptor precursor cells and retinal pigment epithelium. Stem-cell-based therapy is a promising treatment to restore vision in patients with retinal disease, in spite of the challenges.