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عنوان
İnsanda apoptozu düzenleyen uzun kodlamayan RNA'ların moleküler karakterizasyonu

پدید آورنده
Sweef, Osama

موضوع
Apoptosis,Genetics,Molecular biology

رده

کتابخانه
Center and Library of Islamic Studies in European Languages

محل استقرار
استان: Qom ـ شهر: Qom

Center and Library of Islamic Studies in European Languages

تماس با کتابخانه : 32910706-025

NATIONAL BIBLIOGRAPHY NUMBER

Number
TL58204

LANGUAGE OF THE ITEM

.Language of Text, Soundtrack etc
انگلیسی

TITLE AND STATEMENT OF RESPONSIBILITY

Title Proper
İnsanda apoptozu düzenleyen uzun kodlamayan RNA'ların moleküler karakterizasyonu
General Material Designation
[Thesis]
First Statement of Responsibility
Sweef, Osama
Subsequent Statement of Responsibility
Akgül, Bünyamin

.PUBLICATION, DISTRIBUTION, ETC

Name of Publisher, Distributor, etc.
Izmir Institute of Technology (Turkey)
Date of Publication, Distribution, etc.
2019

GENERAL NOTES

Text of Note
149 p.

DISSERTATION (THESIS) NOTE

Dissertation or thesis details and type of degree
Ph.D.
Body granting the degree
Izmir Institute of Technology (Turkey)
Text preceding or following the note
2019

SUMMARY OR ABSTRACT

Text of Note
Apoptosis is an evolutionarily form of programmed cell death for development and tissue homeostasis. Apoptosis is regulated by protein-coding genes and plays an important role in a wide range of biological processes. We aimed to identify and characterize differentially expressed lncRNAs in apoptosis. HeLa cells were used as a model system to identify the lncRNAs. The total RNAs was subjected to deep sequencing by next-generation sequencing. OmicsBOX Bioinformatics tools were used for differential expression analysis of lncRNAs that are apoptosis-induced. Gene set enrichment analysis (GSEA) was used to profile the miRNAs targeting lncRNAs. Cytoscape software was used to reconstruct lncRNA-miRNA targeting networks. RT-qPCR was used to validate miRNAs and their targets of lncRNAs and it was found that the overexpression of miR-519d-3p causes downregulation of lncRNAs RAB22A-202, PARD3-211, and AC027237.1-210. Also, the overexpression of miR-124-3p down-regulates the expression level of APEX2-202 and CD59-209. GTF2A1-AS, TNFRSF10B-AS, and CAMTA1-DT were detected in the nucleus and have no poly (A) tail and they belong to TATA-less promoter genes. TNFRSF10B-AS has a coding probability of 0.99 and alignment to High-scoring Segment Pair (HSP) clarifies one hit to Q9UBN6 protein. ChIRP clarifies that TNFRSF10B-AS binds to a protein (25 kDa). miR-519d-3p and miR-124-3p interact with lncRNA targets by miRNA-mediated lncRNA degradation pattern under apoptosis conditions. TNFRSF10B-AS has a putative regulatory function in the nucleus during apoptosis via binding specifically to the ribonucleoprotein partner.

UNCONTROLLED SUBJECT TERMS

Subject Term
Apoptosis
Subject Term
Genetics
Subject Term
Molecular biology

PERSONAL NAME - PRIMARY RESPONSIBILITY

Sweef, Osama

PERSONAL NAME - SECONDARY RESPONSIBILITY

Akgül, Bünyamin

CORPORATE BODY NAME - SECONDARY RESPONSIBILITY

Izmir Institute of Technology (Turkey)

ELECTRONIC LOCATION AND ACCESS

Electronic name
 مطالعه متن کتاب 

p

[Thesis]
276903

a
Y

Proposal/Bug Report

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