• 제목/요약/키워드: circular RNA

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토마토 뿌리에서 분리한 식물생육촉진과 생물방제 세균 Chryseobacterium sp. T16E-39 균주의 유전체 서열 (Complete genome sequence of Chryseobacterium sp. T16E-39, a plant growth-promoting and biocontrol bacterium, isolated from tomato (Solanum lycopersicum L.) root)

  • 이신애;김상윤;상미경;송재경;원항연
    • 미생물학회지
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    • 제53권4호
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    • pp.351-353
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    • 2017
  • 토마토 뿌리에서 분리한 Chryseobacterium sp. T16E-39 균주는 식물생육촉진과 역병, 시들음병에 대한 억제효과가 있었다. 이 균주의 유전체 염기서열은 4,873,888 염기쌍이었으며 G + C 함량은 35.22%이었다. 이 유전체는 4,289개 단백질 유전자, 15개 rRNA 유전자, 71개 tRNA 유전자를 포함하였다. T16E-39 균주의 유전체에서 인산가용화, 식물호르몬 조절, 항산화 활성, 키틴 분해, 제9형 분비시스템에 관여하는 유전자를 확인하였으며, 이들 유전자는 식물의 생육을 촉진하고 병발생을 억제하는 기작과 관련되어 있을 것으로 판단된다.

Caution and Curation for Complete Mitochondrial Genome from Next-Generation Sequencing: A Case Study from Dermatobranchus otome (Gastropoda, Nudibranchia)

  • Do, Thinh Dinh;Choi, Yisoo;Jung, Dae-Wui;Kim, Chang-Bae
    • Animal Systematics, Evolution and Diversity
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    • 제36권4호
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    • pp.336-346
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    • 2020
  • Mitochondrial genome is an important molecule for systematic and evolutionary studies in metazoans. The development of next-generation sequencing (NGS) technique has rapidly increased the number of mitogenome sequences. The process of generating mitochondrial genome based on NGS includes different steps, from DNA preparation, sequencing, assembly, and annotation. Despite the effort to improve sequencing, assembly, and annotation methods of mitogenome, the low quality and/or quantity sequence in the final map can still be generated through the work. Therefore, it is necessary to check and curate mitochondrial genome sequence after annotation for proofreading and feedback. In this study, we introduce the pipeline for sequencing and curation for mitogenome based on NGS. For this purpose, two mitogenome sequences of Dermatobranchus otome were sequenced by Illumina Miseq system with different amount of raw read data. Generated reads were targeted for assembly and annotation with commonly used programs. As abnormal repeat regions present in the mitogenomes after annotation, primers covering these regions were designed and conventional PCR followed by Sanger sequencing were performed to curate the mitogenome sequences. The obtained sequences were used to replace the abnormal region. Following the replacement, each mitochondrial genome was compared with the other as well as the sequences of close species available on the Genbank for confirmation. After curation, two mitogenomes of D. otome showed a typically circular molecule with 14,559 bp in size and contained 13 protein-coding genes, 22 tRNA genes, two rRNA genes. The phylogenetic tree revealed a close relationship between D. otome and Tritonia diomea. The finding of this study indicated the importance of caution and curation for the generation of mitogenome from NGS.

circRNA circSnx12 confers Cisplatin chemoresistance to ovarian cancer by inhibiting ferroptosis through a miR-194-5p/SLC7A11 axis

  • Kaiyun Qin;Fenghua Zhang;Hongxia Wang;Na Wang;Hongbing Qiu;Xinzhuan Jia;Shan Gong;Zhengmao Zhang
    • BMB Reports
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    • 제56권3호
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    • pp.184-189
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    • 2023
  • Ovarian cancer (OC) is the most common gynecological malignancy worldwide, and chemoresistance occurs in most patients, resulting in treatment failure. A better understanding of the molecular processes underlying drug resistance is crucial for development of efficient therapies to improve OC patient outcomes. Circular RNAs (circRNAs) and ferroptosis play crucial roles in tumorigenesis and resistance to chemotherapy. However, little is known about the role(s) of circRNAs in regulating ferroptosis in OC. To gain insights into cisplatin resistance in OC, we studied the ferroptosis-associated circRNA circSnx12. We evaluated circSnx12 expression in OC cell lines and tissues that were susceptible or resistant to cisplatin using quantitative real-time PCR. We also conducted in vitro and in vivo assays examining the function and mechanism of lnc-LBCSs. Knockdown of circSnx12 rendered cisplatin-resistant OC cells more sensitive to cisplatin in vitro and in vivo by activating ferroptosis, which was at least partially abolished by downregulation of miR-194-5p. Molecular mechanics studies indicate that circSnx12 can be a molecular sponge of miR-194-5p, which targets SLC7A11. According to our findings, circSnx12 ameliorates cisplatin resistance by blocking ferroptosis via a miR-194-5p/SLC7A11 pathway. CircARNT2 may thus serve as an effective therapeutic target for overcoming cisplatin resistance in OC.

Whole genome sequence of Staphylococcus aureus strain RMI-014804 isolated from pulmonary patient sputum via next-generation sequencing technology

  • Ayesha, Wisal;Asad Ullah;Waheed Anwar;Carlos M. Morel;Syed Shah Hassan
    • Genomics & Informatics
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    • 제21권3호
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    • pp.34.1-34.10
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    • 2023
  • Nosocomial infections, commonly referred to as healthcare-associated infections, are illnesses that patients get while hospitalized and are typically either not yet manifest or may develop. One of the most prevalent nosocomial diseases in hospitalized patients is pneumonia, among the leading causes of mortality and morbidity. Viral, bacterial, and fungal pathogens cause pneumonia. More severe introductions commonly included Staphylococcus aureus, which is at the top of bacterial infections, per World Health Organization reports. The staphylococci, S. aureus, strain RMI-014804, mesophile, on-sporulating, and non-motile bacterium, was isolated from the sputum of a pulmonary patient in Pakistan. Many characteristics of S. aureus strain RMI-014804 have been revealed in this paper, with complete genome sequence and annotation. Our findings indicate that the genome is a single circular 2.82 Mbp long genome with 1,962 protein-coding genes, 15 rRNA, 49 tRNA, 62 pseudogenes, and a GC content of 28.76%. As a result of this genome sequencing analysis, researchers will fully understand the genetic and molecular basis of the virulence of the S. aureus bacteria, which could help prevent the spread of nosocomial infections like pneumonia. Genome analysis of this strain was necessary to identify the specific genes and molecular mechanisms that contribute to its pathogenicity, antibiotic resistance, and genetic diversity, allowing for a more in-depth investigation of its pathogenesis to develop new treatments and preventive measures against infections caused by this bacterium.

Comparative Genome Analysis of Psychrobacillus Strain PB01, Isolated from an Iceberg

  • Choi, Jun Young;Kim, Sun Chang;Lee, Pyung Cheon
    • Journal of Microbiology and Biotechnology
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    • 제30권2호
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    • pp.237-243
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    • 2020
  • A novel psychrotolerant Psychrobacillus strain PB01, isolated from an Antarctic iceberg, was comparatively analyzed with five related strains. The complete genome of strain PB01 consists of a single circular chromosome (4.3 Mb) and a plasmid (19 Kb). As potential low-temperature adaptation strategies, strain PB01 has four genes encoding cold-shock proteins, two genes encoding DEAD-box RNA helicases, and eight genes encoding transporters for glycine betaine, which can serve as a cryoprotectant, on the genome. The pan-genome structure of the six Psychrobacillus strains suggests that strain PB01 might have evolved to adapt to extreme environments by changing its genome content to gain higher capacity for DNA repair, translation, and membrane transport. Notably, strain PB01 possesses a complete TCA cycle consisting of eight enzymes as well as three additional Helicobacter pylori-type enzymes: ferredoxin-dependent 2-oxoglutarate synthase, succinyl-CoA/acetoacetyl-CoA transferase, and malate/quinone oxidoreductase. The co-existence of the genes for TCA cycle enzymes has also been identified in the other five Psychrobacillus strains.

Purification and Characterization of Cop, a Protein Involved in the Copy Number Control of Plasmid pE194

  • Kwak, Jin-Hwan;Kim, Jung-Ho;Kim, Mu-Yong;Choi, Eung-Chil
    • Archives of Pharmacal Research
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    • 제21권3호
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    • pp.291-297
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    • 1998
  • Cop protein has been overexpressed in Escherichia coli using a T7 RNA polymerase system. Purification to apparent homogeneity was achieved by the sequential chromatography on ion exchange, affinity chromatography, and reverse phase high performance liquid chromatography system. The molecular weight of the purified Cop was estimated as 6.1 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). But the molecular mass of the native state Cop was shown to be 19 kDa by an analytical high performance size exclusion chromatography, suggesting a trimer-like structure in 50 mM Tris-HCI buffer (pH 7.5) containing 100 mM NaCl. Cop protein Was calculated to contain $39.1% {\alpha}-helix, 16.8% {\beta}-sheet$, 17.4% turn, and 26.8% random structure. The DNA binding property of Cop protein expressed in E. coli Was preserved during the expression and purification process. The isoelectric point of Cop was determined to be 9.0. The results of amino acid composition analysis and N-terminal amino acid sequencing of Cop showed that it has the same amino acid composition and N-terminal amino acid sequence as those deduced from its DNA sequence analysis, except for the partial removal of N-terminal methionine residue by methionyl-aminopeptidase in E. coli.

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First report of gill thelohanellosis from common carp (Cyprinus carpio) fingerling in Korea

  • Mariem BESSAID;Ki Hong Kim
    • 한국어병학회지
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    • 제36권2호
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    • pp.395-401
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    • 2023
  • Myxosporeans are widespread cnidarian endoparasites in marine and freshwater ecosystems and several species were reported to be a threat to cultured fish causing serious diseases with mass mortality. In the present study, we found a myxosporean species in the genus Thelohanellus from the gills of the cultured common carp (Cyprinus carpio) fingerling for the first time in Korea. The morphological observation showed 500 ㎛ ~ 1 mm size, oval to circular shaped plasmodia containing spores which are pyriform at the anterior end and round at the posterior end (average size 20.1 ㎛ × 9.1 ㎛), with 5 to 6 turns of a single polar filament located in the polar capsule with an average size of 10 ㎛ × 4.6 ㎛. The 18S rRNA sequence was closest to the sequence of T. wangi among Thelohanellus species infecting gills but was not completely identical. Based on the morphological characteristics and molecular analysis results, we classified the present myxosporean parasite as Thelohanellus sp., temporarily. The prevalence and infection intensity of Thelohanellus sp. in the common carp fingerling were very high, which was thought to be the main cause of high mortality.

바이로이드-가장 작은 식물병원체 (Viroid-the Smallest Plant Pathogen)

  • 이재열
    • 한국식물병리학회지
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    • 제1권3호
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    • pp.199-206
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    • 1985
  • 바이로이드(viroid)는 그의 완전한 분자구조가 처음으로 밝혀진 식물병원체이며, coat-protein이 제거된 viral-RNA가 아닌 바이로이드로서의 독립적인 특성과 병원성을 가진 작은 크기의 병원체임이 밝혀짐으로써 미생물의 영역을 한 단계 넓혀서 생각하도록 하였다. 일반적으로 생각되는 미생물 즉 곰팡이, 세균, 마이코플라스마, 바이러스들이 동물과 식물 및 인체에 병원체로서 작용하는데 바이로이드는 현재까지 고등식물에서만 발견되는 병원체이다. 다라서 바이로이드가 동물 및 인체에서 아직까지 밝혀지지 않고 있는 병의 병원체일 가능성이 있으므로 이에 대한 연구가 계속되고 있다. 바이로이드는 작은 크기임에도 독자적인 자기증식을 하는 능력과 생존을 유지하는 특성이 있기 때문에 이들의 분자구조 및 생물적 특성을 연구하는데 좋은 자료가 되며, 최근에 급속한 진전을 보이고 있는 분자생물학 및 유전공학적인 방법과 기술을 이용하여 Viroid의 여러 가지 성질과 생물학적인 위치에 대한 연구가 활발히 진행되고 있다. 앞으로 연구가 계속되어 Viroid의 증식과 병원성에 대한 문제가 해결된다면, 바이로이드병의 예방이나 치료법이 확립된 것이며 또한 목적하는 유전자를 운반하는 Vector로 개발하여 생물공학 분야에 적극적으로 활용할 수 있을 것이다.

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해양 생물에서 분리된 Phaeobacter inhibens KJ-2의 항균 활성 (Examination of Antimicrobial Activity by Phaeobacter inhibens KJ-2 Isolated from a Marine Organism)

  • 김윤범;김동휘;허문수
    • 생명과학회지
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    • 제27권10호
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    • pp.1161-1167
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    • 2017
  • 본 연구는 양식업에 막대한 경제적인 손실을 야기시키는 세균성 어류질병인 Vibrio anguillarum을 예방하고 억제하기 위한 목적을 두고, 제주 연안에 서식하는 군소 알로부터 특징적인 균주를 분리 하였다. 이를 16S rRNA 염기서열 분석, 형태학적 특성을 통해 균을 동정하여 Phaeobacter inhibens KJ-2로 명명하였다. Phaeobacter inhibens KJ-2 균주는 Vibrio sp.에 대해 강한 항균 활성을 갖고 있으며, 항균물질의 생산특성을 배양조건에 따라 검토하였으며, 그 결과 진탕 배양의 경우 $20^{\circ}C$에서 24시간 배양 후, 정치 배양의 경우 96시간 배양 후 항균 활성이 가장 높게 나타났다. 진탕 배양 및 정치 배양 모두 4시간 후부터 생육도는 낮았으나 항균 물질 생산을 시작하였다. 생육도가 거의 없는데도 불구하고 항균물질이 생산이 이루어졌는데, 이는 QS (Quorum Sensing)의 신호 물질인 AHLs과 관련이 있다고 사료되며, AHLs의 생성능은 항균 활성과 거의 일치함을 알 수 있었다. 이런 배양특성을 바탕으로 항균 활성을 검토한 결과 V. anguillarum외 다른 Vibrio sp.에 대해서도 항균활성을 나타내었다. 특히 Vibrio vulnificus, Vibrio campbellii, Vibrio mimicus에 대해 높은 저해능을 나타내었다.

부호 영역 DNA 시퀀스 기반 강인한 DNA 워터마킹 (Robust DNA Watermarking based on Coding DNA Sequence)

  • 이석환;권성근;권기룡
    • 전자공학회논문지CI
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    • 제49권2호
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    • pp.123-133
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    • 2012
  • 본 논문에서는 DNA 시퀀스의 불법 복제 및 변이 방지와 개인 정보 침해 방지, 또는 인증을 위한 DNA 워터마킹에 대하여 논의하며, 변이에 강인하고 아미노산 보존성을 가지는 부호영역 DNA 시퀀스 기반 DNA 워터마킹 기법을 제안한다. 제안한 DNA 워터마킹은 부호 영역의 코돈 서열에서 정규 특이점에 해당되는 코돈들을 삽입 대상으로 선택되며, 워터마크된 코돈이 원본 코돈과 동일한 아미노산으로 번역되도록 워터마크가 삽입된다. DNA 염기 서열은 4개의 문자 {A,G,C,T}로 (RNA은 {A,C,G,U}) 구성된 문자열이다. 제안한 방법에서는 워터마킹 신호처리에 적합한 코돈 부호 테이블을 설계하였으며, 이 테이블에 따라 코돈 서열들을 정수열로 변환한 다음 원형 각도 형태의 실수열로 재변환한다. 여기서 코돈은 3개의 염기들로 구성되며, 64개의 코돈들은 20개의 아미노산으로 번역된다. 선택된 코돈들은 아미노산 보존성을 가지는 원형 각도 실수 범위 내에서 인접 코돈과의 원형 거리차 기준으로 워터마크에 따라 변경된다. HEXA와 ANG 시퀀스를 이용한 $in$ $silico$ 실험을 통하여 제안한 방법이 기존 방법에 비하여 아미노산 보존성을 가지면서 침묵 변이와 미스센스 변이에 보다 강인함을 확인하였다.