Literature DB >> 16461945

Simple modifications of the standard DNA sequencing protocol allow for sequencing through siRNA hairpins and other repeats.

Jan Kieleczawa1.   

Abstract

RNAi is a relatively new but powerful technology used for monitoring gene silencing in many species. The RNA corresponding to the gene of interest can be delivered into cells using various protocols, but the approach where both sense and antisense strands are located in the same transcript seems to be the most promising. However, the DNA sequencing step is a challenge due to the formation of a strong hairpin structure. In this work we present a very simple modification to the standard DNA sequencing protocol that allows sequencing through such difficult regions. The modification does not require any additional enzymatic or chemical manipulations. It simply adds a 5-min heat-denaturation step at 98 degrees C, prior to addition of a Taq mix. The inclusion of this step is very effective in sequencing through many different categories of difficult templates. Other examples of the implementation of this step have been described previously and more detailed information on heat-denaturation of plasmid DNAs has been presented.

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Year:  2005        PMID: 16461945      PMCID: PMC2291731     

Source DB:  PubMed          Journal:  J Biomol Tech        ISSN: 1524-0215


  12 in total

Review 1.  Post-transcriptional gene silencing by double-stranded RNA.

Authors:  S M Hammond; A A Caudy; G J Hannon
Journal:  Nat Rev Genet       Date:  2001-02       Impact factor: 53.242

2.  DNA cloning using in vitro site-specific recombination.

Authors:  J L Hartley; G F Temple; M A Brasch
Journal:  Genome Res       Date:  2000-11       Impact factor: 9.043

3.  Short hairpin RNAs (shRNAs) induce sequence-specific silencing in mammalian cells.

Authors:  Patrick J Paddison; Amy A Caudy; Emily Bernstein; Gregory J Hannon; Douglas S Conklin
Journal:  Genes Dev       Date:  2002-04-15       Impact factor: 11.361

4.  Blocking oligonucleotides improve sequencing through inverted repeats.

Authors:  Dominic Esposito; William K Gillette; James L Hartley
Journal:  Biotechniques       Date:  2003-11       Impact factor: 1.993

Review 5.  RNA interference.

Authors:  Gregory J Hannon
Journal:  Nature       Date:  2002-07-11       Impact factor: 49.962

6.  Overcoming obstacles in DNA sequencing of expression plasmids for short interfering RNAs.

Authors:  Daniel C Ducat; Francisco J Herrera; Steven J Triezenberg
Journal:  Biotechniques       Date:  2003-06       Impact factor: 1.993

Review 7.  RNAi and double-strand RNA.

Authors:  P A Sharp
Journal:  Genes Dev       Date:  1999-01-15       Impact factor: 11.361

8.  A system for stable expression of short interfering RNAs in mammalian cells.

Authors:  Thijn R Brummelkamp; René Bernards; Reuven Agami
Journal:  Science       Date:  2002-03-21       Impact factor: 47.728

9.  Role for a bidentate ribonuclease in the initiation step of RNA interference.

Authors:  E Bernstein; A A Caudy; S M Hammond; G J Hannon
Journal:  Nature       Date:  2001-01-18       Impact factor: 49.962

10.  Analysis of gene function in somatic mammalian cells using small interfering RNAs.

Authors:  Sayda M Elbashir; Jens Harborth; Klaus Weber; Thomas Tuschl
Journal:  Methods       Date:  2002-02       Impact factor: 3.608

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  7 in total

1.  Optimization of protocol for sequencing of difficult templates.

Authors:  Jan Kieleczawa; Erica Mazaika
Journal:  J Biomol Tech       Date:  2010-07

2.  Fundamentals of sequencing of difficult templates--an overview.

Authors:  Jan Kieleczawa
Journal:  J Biomol Tech       Date:  2006-07

3.  Identification of optimal protocols for sequencing difficult templates: results of the 2008 ABRF DNA Sequencing Research Group difficult template study 2008.

Authors:  Jan Kieleczawa; Debbie Adam; Doug Bintzler; Michelle Detwiler; David Needleman; Peter Schweitzer; Sushmita Singh; Robert Steen; Michael Zianni
Journal:  J Biomol Tech       Date:  2009-04

4.  Effect of primer proximity to a difficult-to-sequence region on read length and sequence quality.

Authors:  Jan Kieleczawa
Journal:  J Biomol Tech       Date:  2008-12

5.  In ovo electroporation of miRNA-based plasmids in the developing neural tube and assessment of phenotypes by DiI injection in open-book preparations.

Authors:  Nicole H Wilson; Esther T Stoeckli
Journal:  J Vis Exp       Date:  2012-10-16       Impact factor: 1.355

6.  Genotype/Phenotype Relationship in a Consanguineal Family With Brugada Syndrome Harboring the R1632C Missense Variant in the SCN5A Gene.

Authors:  Michelle M Monasky; Emanuele Micaglio; Giuseppe Ciconte; Sara Benedetti; Chiara Di Resta; Gabriele Vicedomini; Valeria Borrelli; Andrea Ghiroldi; Marco Piccoli; Luigi Anastasia; Vincenzo Santinelli; Maurizio Ferrari; Carlo Pappone
Journal:  Front Physiol       Date:  2019-05-28       Impact factor: 4.566

7.  Enhancing the throughput and multiplexing capabilities of next generation sequencing for efficient implementation of pooled shRNA and CRISPR screens.

Authors:  Md Fahmid Islam; Atsushi Watanabe; Lai Wong; Conor Lazarou; Frederick S Vizeacoumar; Omar Abuhussein; Wayne Hill; Maruti Uppalapati; C Ronald Geyer; Franco J Vizeacoumar
Journal:  Sci Rep       Date:  2017-04-21       Impact factor: 4.379

  7 in total

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