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Chromosome and Genomic Engineering in Plants

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Cover of 'Chromosome and Genomic Engineering in Plants'

Table of Contents

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    Book Overview
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    Chapter 1 Production of Engineered Minichromosome Vectors via the Introduction of Telomere Sequences
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    Chapter 2 Method for Biolistic Site-Specific Integration in Plants Catalyzed by Bxb1 Integrase
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    Chapter 3 Protocol for In Vitro Stacked Molecules Compatible with In Vivo Recombinase-Mediated Gene Stacking
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    Chapter 4 Chromosome and Genomic Engineering in Plants
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    Chapter 5 One-Step Generation of Chromosomal Rearrangements in Rice
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    Chapter 6 Genome Elimination by Tailswap CenH3: In Vivo Haploid Production in Arabidopsis thaliana
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    Chapter 7 Chromosome and Genomic Engineering in Plants
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    Chapter 8 CRISPR/Cas-Mediated Site-Specific Mutagenesis in Arabidopsis thaliana Using Cas9 Nucleases and Paired Nickases
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    Chapter 9 Chromosome and Genomic Engineering in Plants
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    Chapter 10 Seamless Genome Editing in Rice via Gene Targeting and Precise Marker Elimination
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    Chapter 11 Chromosome and Genomic Engineering in Plants
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    Chapter 12 Chromosome and Genomic Engineering in Plants
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    Chapter 13 Image Analysis of DNA Fiber and Nucleus in Plants
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    Chapter 14 Chromosome and Genomic Engineering in Plants
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    Chapter 15 Chromosome and Genomic Engineering in Plants
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    Chapter 16 Chromosome and Genomic Engineering in Plants
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    Chapter 17 Mapping of T-DNA and Ac/Ds by TAIL-PCR to Analyze Chromosomal Rearrangements
Attention for Chapter 8: CRISPR/Cas-Mediated Site-Specific Mutagenesis in Arabidopsis thaliana Using Cas9 Nucleases and Paired Nickases
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Chapter title
CRISPR/Cas-Mediated Site-Specific Mutagenesis in Arabidopsis thaliana Using Cas9 Nucleases and Paired Nickases
Chapter number 8
Book title
Chromosome and Genomic Engineering in Plants
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-4931-1_8
Pubmed ID
Book ISBNs
978-1-4939-4929-8, 978-1-4939-4931-1
Authors

Simon Schiml, Friedrich Fauser, Holger Puchta

Abstract

The CRISPR/Cas system has recently become the most important tool for genome engineering due to its simple architecture that allows for rapidly changing the target sequence and its applicability to organisms throughout all kingdoms of life. The need for an easy-to-use and reliable nuclease is especially high in plant research, as precise genome modifications are almost impossible to achieve by Agrobacterium-mediated transformation and the regeneration of plants from protoplast cultures is very labor intensive. Here, we describe the application of the Cas9 nuclease to Arabidopsis thaliana for the induction of heritable targeted mutations, which may also be used for other plant species. To cover the concern for off-target activity, we also describe the generation of stable mutants using paired Cas9 nickases.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 62 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 62 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 12 19%
Student > Ph. D. Student 10 16%
Student > Bachelor 7 11%
Student > Master 7 11%
Student > Doctoral Student 4 6%
Other 5 8%
Unknown 17 27%
Readers by discipline Count As %
Agricultural and Biological Sciences 22 35%
Biochemistry, Genetics and Molecular Biology 18 29%
Medicine and Dentistry 2 3%
Psychology 1 2%
Unknown 19 31%