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Circular RNAs

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Cover of 'Circular RNAs'

Table of Contents

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    Book Overview
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    Chapter 1 Detection and Reconstruction of Circular RNAs from Transcriptomic Data
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    Chapter 2 Deep Computational Circular RNA Analytics from RNA-seq Data
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    Chapter 3 Genome-Wide circRNA Profiling from RNA-seq Data
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    Chapter 4 Analysis of Circular RNAs Using the Web Tool CircInteractome
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    Chapter 5 Characterization and Validation of Circular RNA and Their Host Gene mRNA Expression Using PCR
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    Chapter 6 Detecting Circular RNAs by RNA Fluorescence In Situ Hybridization
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    Chapter 7 Single-Molecule Fluorescence In Situ Hybridization (FISH) of Circular RNA CDR1as
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    Chapter 8 A Highly Efficient Strategy for Overexpressing circRNAs
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    Chapter 9 Constructing GFP-Based Reporter to Study Back Splicing and Translation of Circular RNA
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    Chapter 10 Northern Blot Analysis of Circular RNAs
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    Chapter 11 Nonradioactive Northern Blot of circRNAs
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    Chapter 12 Characterization of Circular RNA Concatemers
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    Chapter 13 Characterization of Circular RNAs (circRNA) Associated with the Translation Machinery
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    Chapter 14 Synthesis and Engineering of Circular RNAs
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    Chapter 15 Preparation of Circular RNA In Vitro
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    Chapter 16 Discovering circRNA-microRNA Interactions from CLIP-Seq Data
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    Chapter 17 Identification of circRNAs for miRNA Targets by Argonaute2 RNA Immunoprecipitation and Luciferase Screening Assays
Attention for Chapter 14: Synthesis and Engineering of Circular RNAs
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Chapter title
Synthesis and Engineering of Circular RNAs
Chapter number 14
Book title
Circular RNAs
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7562-4_14
Pubmed ID
Book ISBNs
978-1-4939-7561-7, 978-1-4939-7562-4
Authors

Sonja Petkovic, Sabine Müller

Abstract

Circular RNAs (circRNAs) have been discovered in all kingdoms of life. They are produced from introns as well as from exons. However, strongest interest is in circRNAs that are transcribed and spliced from exons of protein and noncoding genes in eukaryotic cells including humans. Therefore, synthesis and engineering of circRNAs as models for structure and function studies are strongly required. In vitro, methods for RNA synthesis and circularization are available. Chemical synthesis allows for preparation of RNAs incorporating nonnatural nucleotides in small RNA segments, whereas enzymatic synthesis is advantageous for production of long RNAs, however, without the possibility for site-specific modification. Strategies for chemical and enzymatic RNA synthesis may be combined to obtain long modified linear RNA strands for subsequent circularization. Here, we describe two alternative protocols for synthesis and circularization in dependence on downstream applications and template structure.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 28 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 28 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 18%
Student > Master 5 18%
Student > Bachelor 3 11%
Other 2 7%
Researcher 2 7%
Other 1 4%
Unknown 10 36%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 12 43%
Medicine and Dentistry 2 7%
Business, Management and Accounting 1 4%
Agricultural and Biological Sciences 1 4%
Chemistry 1 4%
Other 0 0%
Unknown 11 39%