• 제목/요약/키워드: TNNC1

검색결과 3건 처리시간 0.02초

Characterization of TNNC1 as a Novel Tumor Suppressor of Lung Adenocarcinoma

  • Kim, Suyeon;Kim, Jaewon;Jung, Yeonjoo;Jun, Yukyung;Jung, Yeonhwa;Lee, Hee-Young;Keum, Juhee;Park, Byung Jo;Lee, Jinseon;Kim, Jhingook;Lee, Sanghyuk;Kim, Jaesang
    • Molecules and Cells
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    • 제43권7호
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    • pp.619-631
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    • 2020
  • In this study, we describe a novel function of TNNC1 (Troponin C1, Slow Skeletal and Cardiac Type), a component of actin-bound troponin, as a tumor suppressor of lung adenocarcinoma (LUAD). First, the expression of TNNC1 was strongly down-regulated in cancer tissues compared to matched normal lung tissues, and down-regulation of TNNC1 was shown to be strongly correlated with increased mortality among LUAD patients. Interestingly, TNNC1 expression was enhanced by suppression of KRAS, and ectopic expression of TNNC1 in turn inhibited KRASG12D-mediated anchorage independent growth of NIH3T3 cells. Consistently, activation of KRAS pathway in LUAD patients was shown to be strongly correlated with down-regulation of TNNC1. In addition, ectopic expression of TNNC1 inhibited colony formation of multiple LUAD cell lines and induced DNA damage, cell cycle arrest and ultimately apoptosis. We further examined potential correlations between expression levels of TNNC1 and various clinical parameters and found that low-level expression is significantly associated with invasiveness of the tumor. Indeed, RNA interference-mediated down-regulation of TNNC1 led to significant enhancement of invasiveness in vitro. Collectively, our data indicate that TNNC1 has a novel function as a tumor suppressor and is targeted for down-regulation by KRAS pathway during the carcinogenesis of LUAD.

가금 근육세포에서 유전자 발현을 유도하는 프로모터 개발 (Development of Promoters Inducing Gene Expression in Poultry Muscle Cells)

  • 강효서;남태희;이우주;이준상;신상수
    • 한국가금학회지
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    • 제50권4호
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    • pp.261-266
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    • 2023
  • 가축의 골격근은 동물성 단백질 식품으로서 중요한 역할을 하며, 가금육의 소비는 전세계적으로 꾸준히 증가하고 있다. 근육의 형성과 발달에는 근형성조절인자를 포함한 많은 유전자들이 관여하며, 발달 단계에 따라 유전자 발현의 정확한 조절이 필요하다. 본 연구에서는 근육에서 특이적으로 발현하는 유전자를 선발하고, 해당 유전자의 프로모터를 클로닝하고 기능을 분석하였다. 동물의 조직별 유전자 발현을 분석한 결과, 다수의 유전자들이 골격근 특이적인 발현양상을 보였는데, 특히 TNNT3와 TNNC2, MYF6 유전자들은 가금에서도 유사한 양상을 나타냈다. TNNT3, TNNC2, MYF6 유전자의 프로모터 부위를 중합효소연쇄반응을 통해 각각 1.2 kb, 1.03 kb, 1.43 kb씩 증폭하여, 녹색형광단백질 유전자를 포함한 벡터의 앞부분에 삽입하였다. 염기서열 분석 결과, 세 프로모터는 기존에 밝혀진 유전체 서열과 거의 일치함을 확인하였다. QM7 메추리 근육세포주에서 각각의 프로모터를 포함한 벡터를 도입한 결과, 세 프로모터 모두녹색형광단백질을 성공적으로 발현시켰다. 녹색 형광의 밝기는 대조군으로 사용한 CMV-IE 프로모터와 비교 시, 약 7배 정도 어두웠다. 클로닝한 프로모터들에는 230개 이상의 전사인자들이 결합할 수 있을 것으로 예측되었으며, 특히 MYF5나 MYOD, MYOG와 같은 근형성조절인자를 포함한 근육에서 발현하는 다양한 전사인자들이 결합할 수 있을 것으로 예측되었다. 이 프로모터들은 가금의 근육세포에서 유전자 발현을 유도하는 연구에 활용이 가능할 것이며, 추후연구를 통해 프로모터 부위별 발현 조절 기능 연구가 필요할 것으로 사료된다.

Muscle differentiation induced up-regulation of calcium-related gene expression in quail myoblasts

  • Park, Jeong-Woong;Lee, Jeong Hyo;Kim, Seo Woo;Han, Ji Seon;Kang, Kyung Soo;Kim, Sung-Jo;Park, Tae Sub
    • Asian-Australasian Journal of Animal Sciences
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    • 제31권9호
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    • pp.1507-1515
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    • 2018
  • Objective: In the poultry industry, the most important economic traits are meat quality and carcass yield. Thus, many studies were conducted to investigate the regulatory pathways during muscle differentiation. To gain insight of muscle differentiation mechanism during growth period, we identified and validated calcium-related genes which were highly expressed during muscle differentiation through mRNA sequencing analysis. Methods: We conducted next-generation-sequencing (NGS) analysis of mRNA from undifferentiated QM7 cells and differentiated QM7 cells (day 1 to day 3 of differentiation periods). Subsequently, we obtained calcium related genes related to muscle differentiation process and examined the expression patterns by quantitative reverse-transcription polymerase chain reaction (qRT-PCR). Results: Through RNA sequencing analysis, we found that the transcription levels of six genes (troponin C1, slow skeletal and cardiac type [TNNC1], myosin light chain 1 [MYL1], MYL3, phospholamban [PLN], caveolin 3 [CAV3], and calsequestrin 2 [CASQ2]) particularly related to calcium regulation were gradually increased according to days of myotube differentiation. Subsequently, we validated the expression patterns of calcium-related genes in quail myoblasts. These results indicated that TNNC1, MYL1, MYL3, PLN, CAV3, CASQ2 responded to differentiation and growth performance in quail muscle. Conclusion: These results indicated that calcium regulation might play a critical role in muscle differentiation. Thus, these findings suggest that further studies would be warranted to investigate the role of calcium ion in muscle differentiation and could provide a useful biomarker for muscle differentiation and growth.