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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 2: Method for Biolistic Site-Specific Integration in Plants Catalyzed by Bxb1 Integrase
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Chapter title
Method for Biolistic Site-Specific Integration in Plants Catalyzed by Bxb1 Integrase
Chapter number 2
Book title
Chromosome and Genomic Engineering in Plants
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-4931-1_2
Pubmed ID
Book ISBNs
978-1-4939-4929-8, 978-1-4939-4931-1
Authors

Ruyu Li, Zhiguo Han, Lili Hou, Gurminder Kaur, Qian Yin, David W. Ow

Abstract

Crop improvement is a never ending process. With a transgenesis approach, it is not inconceivable to envision a continuous addition of new transgenes to existing cultivars. Previously, we described a recombinase-directed gene stacking method in tobacco (Hou et al., Mol Plant 7:1756-1765, 2014). Being able to stack DNA to a previous location ensures that the number of genetic loci does not increase with each new round of transgene addition. Whereas the previous demonstration was conducted through polyethylene glycol to mediate uptake of DNA into tobacco protoplasts, we now describe protocols for using biolistic transformation to stack DNA in tobacco and rice.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 3 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 3 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 2 67%
Unknown 1 33%
Readers by discipline Count As %
Agricultural and Biological Sciences 2 67%
Unknown 1 33%