• 제목/요약/키워드: Heterochromatin formation

검색결과 10건 처리시간 0.023초

Gold and silver plasmonic nanoprobes trace the positions of histone codes

  • Choi, Inhee;Song, Jihwan;Park, Hyunsung
    • BMB Reports
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    • 제55권3호
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    • pp.111-112
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    • 2022
  • We visualized the distribution of heterochromatin in a single nucleus using plasmonic nanoparticle-conjugated H3K9me3 and H3K27me3 antibodies. Due to distance-dependent plasmonic coupling effects between nanoprobes, their scattering spectra shift to longer wavelengths as the distance between heterochromatin histone markers reduced during oncogene-induced senescence (OIS). These observations were supported by simulating scattering profiles based on considerations of particle numbers, interparticle distances, and the spatial arrangements of plasmonic nanoprobes. Using this plasmon-based colourimetric imaging, we estimated changes in distances between H3K9me3 and H3K27me3 during the formation of senescence-associated heterochromatin foci in OIS cells. We anticipate that the devised analytical technique combined with high-spatial imaging and spectral simulation will eventually lead to a new means of diagnosing and monitoring disease progression and cellular senescence.

BMI-1026 treatment can induce SAHF formation by activation of Erk1/2

  • Seo, Hyun-Joo;Park, Hye-Jeong;Choi, Hyung-Su;Hwang, So-Yoon;Park, Jeong-Soo;Seong, Yeon-Sun
    • BMB Reports
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    • 제41권7호
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    • pp.523-528
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    • 2008
  • BMI-1026 is a synthetic aminopyrimidine compound that targets cyclin dependent kinases (cdks) and was initially designed as a potential anticancer drug. Even though it has been well documented that BMI-1026 is a potent cdk inhibitor, little is known about the cellular effects of this compound. In this study, we examined the effects of BMI-1026 treatment on inducing premature senescence and then evaluated the biochemical features of BMI-1026-induced premature senescence. From these experiments we determined that BMI-1026 treatment produced several biochemical features of premature senescence and also stimulated expression of mitogen activated protein kinase (MAPK) family proteins. BMI-1026 treatment caused nuclear translocation of activated Erk1/2 and the formation of senescence associated heterochromatin foci in 5 days. The heterochromatin foci formation was perturbed by inhibition of Erk1/2 activation.

Laser 조사가 망막의 미세구조에 미치는 영향 (The Effect of Laser Irridation on the Ultrastructure of Retina)

  • 김덕훈;문정학
    • 한국안광학회지
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    • 제1권1호
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    • pp.15-22
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    • 1996
  • 본 연구는 망막조직의 미세구조를 전자현미경을 이용하여, 생쥐(ICR)에 대한 Laser 조사의 영향을 조사하였다. 그 결과는 다음과 같다. l. 정상군에서 대개의 망막층은 여러 특수한 세포들과 신경섬유로 구성된 복잡한 구조를 가지고 있었다. 2. Laser 조사의 기간이 길어질수록, 망막의 각 세포의 층과 구조는 일정한 형태를 나타내지 못했다. 시세포 visual cell들은 심하게 이형염색질체 heterochromatin이며, 세포질은 종대되며, 핵의 모양은 불규칙적이며,일부의 세포질은 소실되었다. 망막층의 핵과 신경섬유는 매우 불규칙적이며, 소포의 형성, 각 세포간 경계의 불명확함이 있었다. 색소상피세포 pigment epithelail cell들은 정상모양이 아니며, 세포질에는 큰 공포 형성이 있으며, 핵의 응축과 불규칙한 모양 등이 있었다.

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The role of EZH1 and EZH2 in development and cancer

  • Soo Hyun, Lee;Yingying, Li;Hanbyeol, Kim;Seounghyun, Eum;Kyumin, Park;Chul-Hwan, Lee
    • BMB Reports
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    • 제55권12호
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    • pp.595-601
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    • 2022
  • Polycomb Repressive Complex 2 (PRC2) exhibits key roles in mammalian development through its temporospatial repression of gene expression. EZH1 or EZH2 is the catalytic subunit of PRC2 that mediates the mono-, di- and tri-methylation of histone H3 lysine 27 (H3K27me1/2/3), H3K27me2/me3 being a hallmark of facultative heterochromatin. PRC2 is a chromatin-modifying enzyme that is recruited to a limited number of "nucleation sites", spreads H3K27 methylation and fosters chromatin compaction. EZH1 and EZH2 exhibit differences in their expression patterns, levels of histone methyltransferase activity (HMT) in the context of PRC2, and DNA/nucleosome binding activity. This suggests that their roles in heterochromatin formation are disparate. Dysregulation of PRC2 activity leads to aberrant gene expression and is implicated in cancer and developmental diseases. In this review, we discuss the distinct function of PRC2/EZH1 and PRC2/EZH2 in the early and late developmental stages. We then discuss the cancers associated with PRC2/EZH1 and PRC2/EZH2.

Arsenite induces premature senescence via p53/p21 pathway as a result of DNA damage in human malignant glioblastoma cells

  • Ninomiya, Yasuharu;Cui, Xing;Yasuda, Takeshi;Wang, Bing;Yu, Dong;Sekine-Suzuki, Emiko;Nenoi, Mitsuru
    • BMB Reports
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    • 제47권10호
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    • pp.575-580
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    • 2014
  • In this study, we investigate whether arsenite-induced DNA damage leads to p53-dependent premature senescence using human glioblastoma cells with p53-wild type (U87MG-neo) and p53 deficient (U87MG-E6). A dose dependent relationship between arsenite and reduced cell growth is demonstrated, as well as induced ${\gamma}H2AX$ foci formation in both U87MG-neo and U87MG-E6 cells at low concentrations of arsenite. Senescence was induced by arsenite with senescence-associated ${\beta}$-galactosidase staining. Dimethyl- and trimethyl-lysine 9 of histone H3 (H3DMK9 and H3TMK9) foci formation was accompanied by p21 accumulation only in U87MG-neo but not in U87MG-E6 cells. This suggests that arsenite induces premature senescence as a result of DNA damage with heterochromatin forming through a p53/p21 dependent pathway. p21 and p53 siRNA consistently decreased H3TMK9 foci formation in U87M G-neo but not in U87MG-E6 cells after arsenite treatment. Taken together, arsenite reduces cell growth independently of p53 and induces premature senescence via p53/p21-dependent pathway following DNA damage.

Streptanthus tortus 조직배양 세포에서 사부 영역과 사공의 형성 (Formation of Sieve Element Area and Sieve Pore in Suspension Cultures of Streptanthus tortus)

  • 조봉희
    • 식물조직배양학회지
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    • 제28권2호
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    • pp.109-112
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    • 2001
  • 사부에서 사부영역 또는 사공은 원형질 연락사로부터 형성된다. 사공의 형성은 원형질 연락사에 작은 소포체의 융합 또는 새로 형성된 세포벽의 특정한 장소가 먼저 분해된 후 소포체와 세포벽의 융합으로 형성되었거나, 또는 세포질에서 여러개의 작은 소포체들이 원형으로 모여 서로 융합되면서 형성되었다. 소포체들은 세포 내에 산재해 있는 인이나 이질염 색질에서 합성되었다. 조직배양 세포로부터 유도된 사부나 사공은 일반 식물에 존재하는 사부와 마찬가지로 원통모양이었다. 사공이 다양한 방법으로 형성되며, 사공형성에 필요한 재료는 소포체에서 유래되는 것으로 추정된다.

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Temporal and Spatial Expression Patterns of Nine Arabidopsis Genes Encoding Jumonji C-Domain Proteins

  • Hong, Eun-Hye;Jeong, Young-Min;Ryu, Jee-Youn;Amasino, Richard M.;Noh, Bosl;Noh, Yoo-Sun
    • Molecules and Cells
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    • 제27권4호
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    • pp.481-490
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    • 2009
  • Diverse posttranslational modifications of histones, such as acetylation and methylation, play important roles in controlling gene expression. Histone methylation in particular is involved in a broad range of biological processes, including heterochromatin formation, X-chromosome inactivation, genomic imprinting, and transcriptional regulation. Recently, it has been demonstrated that proteins containing the Jumonji (Jmj) C domain can demethylate histones. In Arabidopsis, twenty-one genes encode JmjC domain-containing proteins, which can be clustered into five clades. To address the biological roles of the Arabidopsis genes encoding JmjC-domain proteins, we analyzed the temporal and spatial expression patterns of nine genes. RT-PCR analyses indicate all nine Arabidopsis thaliana Jmj (AtJmj) genes studied are actively expressed in various tissues. Furthermore, studies of transgenic plants harboring AtJmj::${\beta}$-glucuronidase fusion constructs reveal that these nine AtJmj genes are expressed in a developmentally and spatially regulated manner.

Suppressor of Variegation 3-9 Homolog 2, a Novel Binding Protein of Translationally Controlled Tumor Protein, Regulates Cancer Cell Proliferation

  • Kim, A-Reum;Sung, Jee Young;Rho, Seung Bae;Kim, Yong-Nyun;Yoon, Kyungsil
    • Biomolecules & Therapeutics
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    • 제27권2호
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    • pp.231-239
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    • 2019
  • Suppressor of Variegation 3-9 Homolog 2 (SUV39H2) methylates the lysine 9 residue of histone H3 and induces heterochromatin formation, resulting in transcriptional repression or silencing of target genes. SUV39H1 and SUV39H2 have a role in embryonic development, and SUV39H1 was shown to suppress cell cycle progression associated with Rb. However, the function of human SUV39H2 has not been extensively studied. We observed that forced expression of SUV39H2 decreased cell proliferation by inducing $G_1$ cell cycle arrest. In addition, SUV39H2 was degraded through the ubiquitin-proteasomal pathway. Using yeast two-hybrid screening to address the degradation mechanism and function of SUV39H2, we identified translationally controlled tumor protein (TCTP) as an SUV39H2-interacting molecule. Mapping of the interacting regions indicated that the N-terminal 60 amino acids (aa) of full-length SUV39H2 and the C-terminus of TCTP (120-172 aa) were critical for binding. The interaction of SUV39H2 and TCTP was further confirmed by co-immunoprecipitation and immunofluorescence staining for colocalization. Moreover, depletion of TCTP by RNAi led to up-regulation of SUV39H2 protein, while TCTP overexpression reduced SUV39H2 protein level. The half-life of SUV39H2 protein was significantly extended upon TCTP depletion. These results clearly indicate that TCTP negatively regulates the expression of SUV39H2 post-translationally. Furthermore, SUV39H2 induced apoptotic cell death in TCTP-knockdown cells. Taken together, we identified SUV39H2, as a novel target protein of TCTP and demonstrated that SUV39H2 regulates cell proliferation of lung cancer cells.

Downregulation of JMJD2a and LSD1 is involved in CK2 inhibition-mediated cellular senescence through the p53-SUV39h1 pathway

  • Park, Jeong-Woo;Bae, Young-Seuk
    • BMB Reports
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    • 제55권2호
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    • pp.92-97
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    • 2022
  • Lysine methylation is one of the most important histone modifications that modulate chromatin structure. In the present study, the roles of the histone lysine demethylases JMJD2a and LSD1 in CK2 downregulation-mediated senescence were investigated. The ectopic expression of JMJD2a and LSD1 suppressed the induction of senescence-associated β-galactosidase activity and heterochromatin foci formation as well as the reduction of colony-forming and cell migration ability mediated by CK2 knockdown. CK2 downregulation inhibited JMJD2a and LSD1 expression by activating the mammalian target of rapamycin (mTOR)-ribosomal p70 S6 kinase (p70S6K) pathway. In addition, the down-regulation of JMJD2a and LSD1 was involved in activating the p53-p21Cip1/WAF1-SUV39h1-trimethylation of the histone H3 Lys9 (H3K9me3) pathway in CK2-downregulated cells. Further, CK2 downregulation-mediated JMJD2a and LSD1 reduction was found to stimulate the dimethylation of Lys370 on p53 (p53K370me2) and nuclear import of SUV39h1. Therefore, this study indicated that CK2 downregulation reduces JMJD2a and LSD1 expression by activating mTOR, resulting in H3K9me3 induction by increasing the p53K370me2-dependent nuclear import of SUV39h1. These results suggest that CK2 is a potential therapeutic target for age-related diseases.

양서루 피부 과립선의 미세구조 (Ultrastructure of the Granular Glands in the Amphibian Skin)

  • 김한화;노용태;정영화;지영득
    • 한국동물학회지
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    • 제22권3호
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    • pp.103-114
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    • 1979
  • 양서류 피부과립선의 미세구조를 관찰하기 위하여 무미양서류인 무당개구리(Bombina orientalis), 두꺼비 (Bufo bufo gargarizans), 개구리 (Rana nigromaculata) 및 옴개구리 (Rana rugosa)의 피부조직은 2.5% glutaraldehyde-paraformaldehyde (pH 7.2)와 1%osmium tetroxide에 전후 고정한 후 ethanol과 acetone으로 탈수, Epon 812 mixture에 포매하여 LKB ultramicrotome으로 초박절표본을 만들어 uranyl acetate와 lead citrate으로 염색하여 JEOL-100B형 전자현미경으로 관찰하여 다음과 같은 결과를 얻었다. 1. 양서류 피부과립선은 선상피세포와 근상피세포로 이루어졌다. 2. 양서류 피부과립선의 선상피세포는 암세포들로 구성되었으나 무당개구리에서는 명세포도 관찰되었다. 3. 양서류 피부과립선은 전분지를 하였다. 4. 양서류 피부과립선 상피세포의 핵은 원형 내지 타원형으로 크고 작은 핵경함요를 보였고, heterochromatin은 주로 핵경 인접부에 많았다. 세포질에는 mitochondria가 핵주변부에 비교적 많이 산재하였고, rough-surfaced endoplasmic reticulum은 핵 주변부에 발달하였지만 smooth-surfaced endoplasmic reticulum은 미약하였다. 5. 분비과립들은 구형 또는 난형으로 높은 전자밀도를 보였으며 다소 약한 전자밀도를 보이는 과립도 관찰되었다. 6. 양서류 과립선내 분비과립들이 같은 세포내에서 다소 전자밀도의 차이를 보이는 것은 분비과립의 형성단계에 따른 농도 차이에 기인하며 그 화학적 조성은 유사하다고 생각된다.

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