MYC MEME KANSERI HÜCRELERINDE tRNA’LARIN IFADESINI REGÜLE EDER

Yıl 2023, , 88 - 95, 28.02.2023

Pervin Elvan Tokgün , Onur Tokgün

https://doi.org/10.26650/JARHS2023-1199491

Öz

Amaç: Protein sentezi süreci, DNA’nın çekirdekte mRNA’ya kopyalanmasıyla başlar, ardından mRNA, bir proteine çevrilmek üzere sitoplazmaya taşınır ve ribozoma bağlanır. Protein sentezi sadece sitoplazmada gerçekleşmez. Mitokondri de kendi genetik sistemine sahiptir. Bu nedenle mtDNA’da replikasyon, transkripsiyon ve translasyon gerçekleşir. MYC onkogeni, birçok kanser türünün gelişimine neden olur. MYC ayrıca ribozom biyogenezi ve protein sentezi ile ilgili bazı hedef genleri kontrol eder. tRNA sentetazlarının artan ifadelerinin, çeşitli insan kanseri türlerinde tümör büyümesini desteklemede önemli rolü olduğu bulunmuştur. Bu çalışmada, nükleus ve mitokondride görev yapan tRNA‘ların MYC’e bağımlı ifadelerini belirlemeyi amaçladık. Gereç ve Yöntem: Hücreler lentiviral MYC overekspresyon/shRNA vektörleri ile infekte edildi. RNA izolasyonu için TRIZOL reaktifi kullanıldı ve yeni nesil dizileme için kütüphaneler hazırlandı. RNA örneklerinin ve kütüphanelerin kalitesi, Agilent BioAnalyzer kullanılarak değerlendirildi. Dizileme, Illumina HT2500 platformunda yapıldı. Bulgular: Meme kanseri hücrelerinde MYC ifade değişimine bağlı olarak 65 nuklear tRNA ve 6 nükleer kodlanmış mitokondriyal tRNA saptadık. Sonuç: Bu çalışma, meme kanserinde tRNA‘ların MYC‘e bağlı regülasyonunu ortaya koymaktadır. Moleküler mekanizmaların aydınlatılması için daha ileri fonksiyonel çalışmalar gereklidir.

Anahtar Kelimeler

tRNA, yeni nesil dizileme, meme kanseri

Destekleyen Kurum

Pamukkale Üniversitesi BAP

Proje Numarası

2016HZDP006

DEREGULATED EXPRESSIONS OF MYC ALTER THE EXPRESSIONS OF tRNAS IN BREAST CANCER CELLS

Öz

Objective: The protein synthesis process is started with DNA being transcribed into mRNA in the nucleus, then mRNA is transported to the cytoplasm and attaches to a ribosome in order to be translated into a protein. Protein synthesis not only occurs in the cytoplasm. Mitochondria by itself also has its own genetic system. Therefore mtDNA can be replicated, transcribed, and translated. MYC oncogene drives the generation of many cancer types. MYC also controls some target genes related to ribosome biogenesis and protein synthesis. Increased expressions of tRNA synthetases have been found to be important players in promoting tumor growth in various types of human cancers. In this study we aimed to identify deregulated expressions of tRNAs that are players both in the nucleus and mitochondria in a MYC-dependent manner in breast cancer cells. Material and Methods: Cells were infected with lentiviral MYC shRNA/ overexpression vectors in order to manipulate MYC expressions. TRIZOL reagent was used for RNA isolation and libraries were generated for sequencing. The quality of the RNA samples and libraries was assessed using Agilent BioAnalyzer. Sequencing was performed on the Illumina HT2500 platform. Results: We obtained 6 nuclear-encoded mitochondrial tRNAs and 65 nuclear tRNAs as a result of deregulated expression of MYC. Conclusion: This study reveals MYC-dependent regulation of tRNAs in breast cancer. Further functional studies are required for underlying molecular mechanisms.

Anahtar Kelimeler

tRNA, next-generation sequencing, breast cancer

Proje Numarası

2016HZDP006

Kaynakça

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