• 제목/요약/키워드: 3 'UTR

검색결과 215건 처리시간 0.024초

MiRNA-15a Mediates Cell Cycle Arrest and Potentiates Apoptosis in Breast Cancer Cells by Targeting Synuclein-γ

  • Li, Ping;Xie, Xiao-Bing;Chen, Qian;Pang, Guo-Lian;Luo, Wan;Tu, Jian-Cheng;Zheng, Fang;Liu, Song-Mei;Han, Lu;Zhang, Jian-Kun;Luo, Xian-Yong;Zhou, Xin
    • Asian Pacific Journal of Cancer Prevention
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    • 제15권16호
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    • pp.6949-6954
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    • 2014
  • Background: Recent studies have indicated that microRNA-15a (miR-15a) is dysregulated in breast cancer (BC). We aimed to evaluate the expression of miR-15a in BC tissues and corresponding para-carcinoma tissues. We also focused on effects of miR-15a on cellular behavior of MDA-MB-231 and expression of its target gene synuclein-${\gamma}$ (SNCG). Materials and Methods: The expression levels of miR-15a were analysed in BC formalin fixed paraffin embedded (FFPE) tissues by microarray and quantitative real-time PCR. CCK-8 assays, cell cycle and apoptosis assays were used to explore the potential functions of miR-15a in MDA-MB-231 human BC cells. A luciferase reporter assay confirmed direct targets. Results: Downregulation of miR-15a was detected in most primary BCs. Ectopic expression of miR-15a promoted proliferation and suppressed apoptosis in vivo. Further studies indicated that miR-15a may directly interact with the 3'-untranslated region (3'-UTR) of SNCG mRNA, downregulating its mRNA and protein expression levels. SNCG expression was negatively correlated with miR-15a expression. Conclusions: MiR-15a has a critical role in mediating cell cycle arrest and promoting cell apoptosis of BC, probably by directly targeting SNCG. Thus, it may be involved in development and progression of BC.

Candida albicans의 마이크로RNA 동정과 분석 (Identification and analysis of microRNAs in Candida albicans)

  • 조진현;이헌진
    • 생명과학회지
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    • 제27권12호
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    • pp.1494-1499
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    • 2017
  • Candida albicans에 의한 구강 감염(캔디다증)은 구강 점막에 빈번하게 발생하며 잘 알려진 질병이다. 구강 캔디다증은 생명을 위협하는 정도의 곰팡이 감염증은 아니나, 특정상황에서 개인에게 심각한 위험을 초래할 수도 있다. 마이크로 RNA는 세포 내에서 다른 타겟 유전자를 저해하는 작은 크기의 RNA 분자이며 단백질을 코딩하지는 않고 번역과정을 억제하는 조절자로서의 역할을 하고 있다. 본 연구는 C. albicans의 마이크로RNA를 처음으로 동정하고 그러한 마이크로RNA가 지닌 기능을 조사하기 위함이다. 이를 위하여 C. albicans의 small RNA를 차세대 염기분석법을 통하여 분석하고 그러한 RNA들의 2차 구조를 생물정보학적 방법으로 조사하였다. 분석한 small RNA들은 마이크로 RNA라고 불리울 수 있는 특징들을 가지고 있었으며, 특별히 높게 발현되고 있는 두개의 마이크로 RNA 정도 크기의 RNA가 CBP1 유전자의 3' 말단 비번역구역(UTR)에서 반대방향으로 발현하는 것을 밝혀 내었다. 우리는 이러한 C. albicans의 RNA가 CBP1 유전자를 타겟으로 하여 조절하는지 알아보기 위해 RNA를 인위적으로 합성한 후 세포 내로 주입하고, 형광형미경으로 도입 사실을 확인하였다. 하지만 4시간과 8시간 후에 CBP1의 발현 변화는 관찰되지 않았다. 따라서, 이러한 결과는 C. albicans가 마이크로RNA에 의한 RNA 간섭(RNAi) 작용이 다른 진핵세포와는 다르게 작용하는 것을 알 수 있다.

감마선 처리에 의한 스프레이형 국화 화색변이체로부터 Flavonoid 3'-Hydroxylase(F3'H) 유전자의 분리 및 특성 구명 (Isolation and Characterization of a Novel Flavonoid 3'-Hydroxylase (F3'H) Gene from a Chrysanthemum (Dendranthema grandiflorum) and Its Gamma-ray Irradiated Mutants)

  • 정성진;이긍주;김진백;김동섭;김상훈;강시용
    • 원예과학기술지
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    • 제30권2호
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    • pp.162-170
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    • 2012
  • 스프레이 국화품종 'Argus'와 감마선 조사에 의해 화색변이가 일어난 돌연변이체의 꽃잎으로부터 안토시아닌 생합성 경로에서 중요한 역할을 담당하는 신규 $DgF3'H$의 전장 cDNA와 genomic DNA를 분리하였다. 전장 cDNA는 1,527bp(509 아미노산)의 ORF를 포함하고 있으며, 원품종 'Argus'와 화색변이체 사이의 염기서열 상동성은 97% 이상을 나타내었다. Genomic DNA의 크기는 야생형 'Argus'에서 3,831bp이었고, 3가지 화색 변이체에서는 3,828부터 3,838bp의 크기를 나타내었다. $DgF3'H$ 유전자는 세 개의 exon사이에 두개의 intron을 갖고 있는 구조이고, 3'과 5' UTR 부분을 제외한 intron의 크기는 야생형 'Argus'에서 2,157bp이지만 3가지 화색 변이체에서는 2,155부터 2,159bp의 크기를 갖고 있었다. 이것은 감마선 조사에 의해 intron 부분의 유전자가 결실 또는 삽입된 것으로 추정된다. Southern 분석 결과 국화의 genome 내에서는 복수의 F3'H 유전자를 갖는 것이 확인되었다. $DgF3'H$ 유전자의 발현 정도를 분석한 결과, 연분홍의 'Argus'와 두 개의 보라색 변이체(AM1 and AM3)에서 높게 발현되었으나 흰색 변이체(AM2)에서는 매우 약하게 발현되었으며, 염기서열 변이에 의한 F3'H 유전자의 구조적 차이가 화색의 변이에 관련된 것으로 추정되었다. 국화 'Argus' 및 화색 변이체를 이용하여 본 연구에서 분리한 신규 F3'H 유전자의 구조 및 유전자 발현 등을 포함하는 유전정보들은 화색 변이의 유전적 기작을 밝히는데 중요한 자료로 이용될 것으로 기대되나 향후 다른 유전적 발현요소들이 국화의 F3'H 유전자의 발현에 관여하는지에 관한 추가적인 연구가 필요하다고 하겠다.

miR-200a Inhibits Tumor Proliferation by Targeting AP-2γ in Neuroblastoma Cells

  • Gao, Shun-Li;Wang, Li-Zhong;Liu, Hai-Ying;Liu, Dan-Li;Xie, Li-Ming;Zhang, Zhi-Wei
    • Asian Pacific Journal of Cancer Prevention
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    • 제15권11호
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    • pp.4671-4676
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    • 2014
  • Background: MicroRNA-200a (miR-200a) has been reported to regulate tumour progression in several tumours but little is known about its role in neuroblastoma. Our aim was to investigate the potential role and mechanism of miR-200a in neuroblastomas. Materials and Methods: Expression levels of miR-200a in tissues were determined using RT-PCR. The effect of miR-200a and shAP-$2{\gamma}$ on cell viability was evaluated using MTS assays, and target protein expression was determined using Western blotting and RT-PCR. Luciferase reporter plasmids were constructed to confirm direct targeting. Results were reported as mean${\pm}$S.E.M and differences were tested for significance using the 2-tailed Students t-test. Results: We determined that miR-200a expression was significantly lower in neuroblastoma tumors than the adjacent non-cancer tissue. Over-expression of miR-200 are reduced cell viability in neuroblastoma cells and inhibited tumor growth in mouse xenografts. We identified AP-$2{\gamma}$ as a novel target for miR-200a in neuroblastoma cells. Thus miR-200a targets the 3'UTR of AP-$2{\gamma}$ and inhibits its mRNA and protein expression. Furthermore, our result showed that shRNA knockdown of AP-$2{\gamma}$ in neuroblastoma cells results in significant inhibit of cell proliferation and tumor growth in vitro, supporting an oncogenic role of AP-$2{\gamma}$ in neuroblastoma. Conclusions: Our study revealed that miR-200a is a candidate tumor suppressor in neuroblastoma, through direct targeting of AP-$2{\gamma}$. These findings re-enforce the proposal of AP-$2{\gamma}$ as a therapeutic target in neuroblastoma.

마(Dioscorea opposita)에 발생한 Japanese yam mosaic virus 진단 및 염기서열 분석 (Diagnosis and Sequence Analysis of Japanese yam mosaic virus from Yam (Dioscorea opposita))

  • 이중환;손창기;권중배;남효훈;김영태;김미경;이수헌
    • 식물병연구
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    • 제22권4호
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    • pp.289-292
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    • 2016
  • JYMV에 감염된 마는 잎과 엽맥에 부정형의 황화증상을 나타내었고, 마 주산단지인 경북 안동지역에서 조사한 결과 33.6%-40.8%의 감염률을 나타냈다. 마에 발생하는 JYMV 분리주 BRI 게놈의 polyprotein을 코딩하는 영역에 대한 염기서열을 결정하고 이를 JYMV isolate BRI로 명명하고 GenBank에 KU309315로 유전자 등록을 하였으며, 외피단백질 영역에 대한 유연관계 분석에서 대부분의 일본이나 중국과 분리주와는 다른 유연관계를 보이는데 이것은 분화 과정 중에 나타나는 변이주 가능성이 제시되나 추후 광범위한 조사를 통한 정밀한 분석이 필요하다.

Down Regulation of miR-34a and miR-143 May Indirectly Inhibit p53 in Oral Squamous Cell Carcinoma: a Pilot Study

  • Manikandan, Mayakannan;Rao, Arunagiri Kuha Deva Magendhra;Arunkumar, Ganesan;Rajkumar, Kottayasamy Seenivasagam;Rajaraman, Ramamurthy;Munirajan, Arasambattu Kannan
    • Asian Pacific Journal of Cancer Prevention
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    • 제16권17호
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    • pp.7619-7625
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    • 2015
  • Background: Aberrant microRNA expression has been associated with the pathogenesis of a variety of human malignancies including oral squamous cell carcinoma (SCC). In this study, we examined primary oral SCCs for the expression of 6 candidate miRNAs, of which five (miR-34a, miR-143, miR-373, miR-380-5p, and miR-504) regulate the tumor suppressor TP53 and one (miR-99a) is involved in AKT/mTOR signaling. Materials and Methods: Tumor tissues (punch biopsies) were collected from 52 oral cancer patients and as a control, 8 independent adjacent normal tissue samples were also obtained. After RNA isolation, we assessed the mature miRNA levels of the 6 selected candidates against RNU44 and RNU48 as endogenous controls, using specific TaqMan miRNA assays. Results: miR-34a, miR-99a, miR-143 and miR-380-5p were significantly down-regulated in tumors compared to controls. Moreover, high levels of miR-34a were associated with alcohol consumption while those of miR-99a and miR-143 were associated with advanced tumor size. No significant difference was observed in the levels of miR-504 between the tumors and controls whereas miR-373 was below the detection level in all but two tumor samples. Conclusions: Low levels of miR-380-5p and miR-504 that directly target the 3'UTR of TP53 suggest that p53 may not be repressed by these two miRNAs in OSCC. On the other hand, low levels of miR-34a or miR-143 may relieve MDM4 and SIRT1 or MDM2 respectively, which will sequester p53 indicating an indirect mode of p53 suppression in oral tumors.

Novel Polymorphisms of Adrenergic, Alpha-1B-, Receptor and Peroxisome Proliferator-activated Receptor Gamma, Coactivator 1 Beta Genes and Their Association with Egg Production Traits in Local Chinese Dagu Hens

  • Mu, F.;Jing, Y.;Qin, N.;Zhu, H.Y.;Liu, D.H.;Yuan, S.G.;Xu, R.F.
    • Asian-Australasian Journal of Animal Sciences
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    • 제29권9호
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    • pp.1256-1264
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    • 2016
  • Adrenergic, alpha-1B-, receptor (ADRA1B) and peroxisome proliferator-activated receptor gamma, coactivator 1 beta (PPARGC1B) genes are involved in regulation of hen ovarian development. In this study, these two genes were investigated as possible molecular markers associated with hen-housed egg production, egg weight (EW) and body weight in Chinese Dagu hens. Samples were analyzed using the polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) technique, followed by sequencing analysis. Two novel single nucleotide polymorphisms (SNPs) were identified within the candidate genes. Among them, an A/G transition at base position 1915 in exon 2 of ADRA1B gene and a T/C mutation at base position 6146 in the 3'- untranslated region (UTR) of PPARGC1B gene were found to be polymorphic and named SNP A1915G and T6146C, respectively. The SNP A1915G (ADRA1B) leads to a non-synonymous substitution (aspartic acid 489-to-glycine). The 360 birds from the Dagu population were divided into genotypes AA and AG, allele A was found to be present at a higher frequency. Furthermore, the AG genotype correlated with significantly higher hen-housed egg production (HHEP) at 30, 43, 57, and 66 wks of age and with a higher EW at 30 and 43 wks (p<0.05). For the SNP T6146C (PPARGC1B), the hens were typed into TT and TC genotypes, with the T allele shown to be dominant. The TC genotype was also markedly correlated with higher HHEP at 57 and 66 wks of age and EW at 30 and 43 wks (p<0.05). Moreover, four haplotypes were reconstructed based on these two SNPs, with the AGTC haplotype found to be associated with the highest HHEP at 30 to 66 wks of age and with higher EW at 30 and 43 wks (p<0.05). Collectively, the two SNPs identified in this study might be used as potential genetic molecular markers favorable in the improvement of egg productivity in chicken breeding.

Roles of E-Cadherin (CDH1) Genetic Variations in Cancer Risk: a Meta-analysis

  • Deng, Qi-Wen;He, Bang-Shun;Pan, Yu-Qin;Sun, Hui-Ling;Xu, Ye-Qiong;Gao, Tian-Yi;Li, Rui;Song, Guo-Qi;Wang, Shu-Kui
    • Asian Pacific Journal of Cancer Prevention
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    • 제15권8호
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    • pp.3705-3713
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    • 2014
  • E-Cadherin (CDH1) genetic variations may be involved in invasion and metastasis of various cancers by altering gene transcriptional activity of epithelial cells. However, published studies on the association of CDH1 gene polymorphisms and cancer risk remain contradictory, owing to differences in living habits and genetic backgrounds. To derive a more better and comprehensive conclusion, the present meta-analysis was performed including 57 eligible studies of the association between polymorphisms of CDH1 gene promoter -160 C>A, -347 G>GA and 3'-UTR +54 C>T and cancer risk. Results showed that these three polymorphisms of CDH1 were significantly associated with cancer risk. For -160 C>A polymorphism, -160A allele carriers (CA and CA+AA) had an increased risk of cancer compared with the homozygotes (CC), and the similar result was discovered for the -160A allele in the overall analyses. In the subgroup analyses, obvious elevated risk was found with -160A allele carriers (AA, CA, CA+AA and A allele) for prostate cancer, while a decreased colorectal cancer risk was shown with the AA genotype. For the -347 G>GA polymorphism, the GAGA genotype was associated with increased cancer risk in the overall analysis with homozygous and recessive models. In addition, results of subgroup analysis indicated that the elevated risks were observed in colorectal cancer and Asian descendants. For +54 C>T polymorphism, a decreased risk of cancer was found in heterozygous, dominant and allele models. Moreover, +54T allele carriers (CT, CT+TT genotype and T allele) showed a potential protective factor in gastric cancer and Asian descendants.

MicroRNA-3200-5p Promotes Osteosarcoma Cell Invasion via Suppression of BRMS1

  • Li, Gen;Li, Li;Sun, Qi;Wu, Jiezhou;Ge, Wei;Lu, Guanghua;Cai, Ming
    • Molecules and Cells
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    • 제41권6호
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    • pp.523-531
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    • 2018
  • Tumour metastasis is one of the most serious challenges of cancer as it is the major cause of mortality in patients with solid tumours, including osteosarcoma (OS). In this regard, anti-metastatic genes have potential for metastasis inhibition strategies. Recent evidence showed the importance of breast cancer metastasis suppressor 1 (BRMS1) in control of OS invasiveness, but the regulation of BRMS1 in OS remains largely unknown. Here, we used bioinformatics analyses to predict BRMS1-targeting microRNAs (miRNAs), and the functional binding of miRNAs to BRMS1 mRNA was evaluated using a dual luciferase reporter assay. Among all BRMS1-targeting miRNAs, only miR-151b, miR-7-5p and miR-3200-5p showed significant expression in OS specimens. Specifically, we found that only miR-3200-5p significantly inhibited protein translation of BRMS1 via pairing to the 3'-UTR of the BRMS1 mRNA. Moreover, we detected significantly lower BRMS1 and significantly higher miR-3200-5p in the OS specimens compared to the paired adjacent non-tumour bone tissues. Furthermore, BRMS1 and miR-3200-5p levels were inversely correlated to each other. Low BRMS1 was correlated with metastasis and poor patient survival. In vitro, overexpression of miR-3200-5p significantly decreased BRMS1 levels and promoted OS cell invasion and migration, while depletion of miR-3200-5p significantly increased BRMS1 levels and inhibited OS cell invasion and migration. Thus, our study revealed that miR-3200-5p may be a critical regulator of OS cell invasiveness.

T-DNA 삽입에 의한 Formaldehyde-Responsive Protein1 기능파괴 돌연변이체의 특성연구 (Characterization of T-DNA Insertional Mutant of Formaldehyde-Responsive Protein1)

  • 서재현;우수영;김욱;권미
    • 한국산림과학회지
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    • 제99권4호
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    • pp.501-507
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    • 2010
  • Formaldehyde responsive protein1(FRP1)은 175개의 아미노산으로 이루어진 universal stress protein(USP) family이며 대표적인 대기오염물질인 포름알데히드에 반응하는 단백질로 보고된 바 있다. 하지만 FRP1의 기능에 관해서는 전혀 밝혀진 바가 없다. 본 연구에서는 FRP1의 대기오염관련 기능연구를 위하여 FRP1 유전자에 T-DNA가 삽입된 돌연변이체를 분리하여 휘발성 유기화합물에 대한 반응성 및 세포활성변화 등을 분석하였다. 총 4개의 T-DNA 삽입 돌연변이 개체를 분석한 결과 3'UTR에 pROK2 vector가 삽입된 frp1-4 라인을 분리하였으며, frp1-4에서의 FRP1 유전자의 발현을 전사수준에서 분석한 결과 분리한 frp1-4은 FRP1 기능파괴 돌연변이체임을 알 수 있었다. FRP1의 전사가 억제됨에 따라 frp1-4($29.1{\pm}2.55$ cm)은 대조구($33.75{\pm}1.55$ cm)에 비해 키가 약간 작고 rosette leaves의 크기가 줄어드는 등 전체적으로 생장과 발달이 저해되는 것을 관찰할 수 있었다. 대조구와 frp1-4의 휘발성 유기화합물에 대한 반응성 및 세포활성 변화를 분석한 결과, 대조구는 포름알데히드 처리에 의한 엽록소 함량 저하가 7.5% 임에 반해 frp1-4은 35%에 이르러 포름알데히드에 의한 엽록소의 파괴현상이 FRP1의 기능파괴체에서 더 심각하게 발생하는 것을 확인하였다. 또한 대조구에 비해 frp1-4에서 포름알데히드 처리에 의한 세포활성의 감소가 대조구에 비해 더 현저하게 나타나는 것을 세포수준에서 관찰할 수 있었다. 그러므로 FRP1은 식물의 발달과 생장에 영향을 끼칠 뿐만 아니라 대기오염물질에 대한 스트레스 저항성에도 관여하는 단백질임을 알 수 있었다.