scholarly journals Reverse Genetic Strategies inCaenorhabditis elegans: Towards Controlled Manipulation of the Genome

2011 ◽  
Vol 11 ◽  
pp. 1394-1410 ◽  
Author(s):  
Howard A. Baylis ◽  
Rafael P. Vázquez-Manrique

Caenorhabditis eleganshas a complete annotated genome sequence that is augmented by increasing quantities of data from high-throughput postgenomic analyses. This has led to an increasing need to identify the biological functions of specific genes using reverse genetics, i.e., moving from gene to phenotype. Fundamental to this aim is the ability to alter the structure of particular genes by means that are not accessible to classical genetic strategies. Thus, one dream ofC. elegansresearchers is to establish a toolkit for the controlled manipulation of anylociwithin the genome. AlthoughC. elegansis amenable to a wide variety of genetic and molecular manipulations, controlled manipulation of endogenous genes by, for example, gene targeting has proved elusive until relatively recently. In this review, we describe and discuss the different methods available for the inactivation and modification of endogenous loci with a focus on strategies that permit some measure of control in this process. We describe methods that use random mutagenesis to isolate mutations in specific genes. We then focus on techniques that allow controlled manipulation of the genome: gene modification by transposon mobilisation, gene knock-out mediated by zinc-finger nucleases, and gene targeting by biolistic transformation.

Genomics ◽  
2010 ◽  
Vol 95 (1) ◽  
pp. 37-46 ◽  
Author(s):  
Rafael P. Vázquez-Manrique ◽  
James C. Legg ◽  
Birgitta Olofsson ◽  
Sung Ly ◽  
Howard A. Baylis

2003 ◽  
pp. 205-216
Author(s):  
Ichiro Sora ◽  
Kazutaka Ikeda ◽  
Yuji Mishina

2013 ◽  
Vol 3 (10) ◽  
pp. 1717-1725 ◽  
Author(s):  
Kelly J. Beumer ◽  
Jonathan K. Trautman ◽  
Michelle Christian ◽  
Timothy J. Dahlem ◽  
Cathleen M. Lake ◽  
...  

2020 ◽  
Vol 11 ◽  
Author(s):  
Yuan Zhang ◽  
Allan M. Showalter

For the past 5 years, clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9 (CRISPR/Cas9) technology has appeared in the molecular biology research spotlight. As a game-changing player in genome editing, CRISPR/Cas9 technology has revolutionized animal research, including medical research and human gene therapy as well as plant science research, particularly for crop improvement. One of the most common applications of CRISPR/Cas9 is to generate genetic knock-out mutants. Recently, several multiplex genome editing approaches utilizing CRISPR/Cas9 were developed and applied in various aspects of plant research. Here we summarize these approaches as they relate to plants, particularly with respect to understanding the biosynthesis and function of the plant cell wall. The plant cell wall is a polysaccharide-rich cell structure that is vital to plant cell formation, growth, and development. Humans are heavily dependent on the byproducts of the plant cell wall such as shelter, food, clothes, and fuel. Genes involved in the assembly of the plant cell wall are often highly redundant. To identify these redundant genes, higher-order knock-out mutants need to be generated, which is conventionally done by genetic crossing. Compared with genetic crossing, CRISPR/Cas9 multi-gene targeting can greatly shorten the process of higher-order mutant generation and screening, which is especially useful to characterize cell wall related genes in plant species that require longer growth time. Moreover, CRISPR/Cas9 makes it possible to knock out genes when null T-DNA mutants are not available or are genetically linked. Because of these advantages, CRISPR/Cas9 is becoming an ideal and indispensable tool to perform functional studies in plant cell wall research. In this review, we provide perspectives on how to design CRISPR/Cas9 to achieve efficient gene editing and multi-gene targeting in plants. We also discuss the recent development of the virus-based CRISPR/Cas9 system and the application of CRISPR/Cas9 to knock in genes. Lastly, we summarized current progress on using CRISPR/Cas9 for the characterization of plant cell wall-related genes.


2008 ◽  
Vol 105 (50) ◽  
pp. 19821-19826 ◽  
Author(s):  
K. J. Beumer ◽  
J. K. Trautman ◽  
A. Bozas ◽  
J.-L. Liu ◽  
J. Rutter ◽  
...  

2010 ◽  
Vol 150 ◽  
pp. 474-475
Author(s):  
A Tovkach ◽  
V Zeevi ◽  
D Weinthal ◽  
T Tzfira

2005 ◽  
Vol 23 (8) ◽  
pp. 967-973 ◽  
Author(s):  
Matthew H Porteus ◽  
Dana Carroll

2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Brian D. Janssen ◽  
Yi-Pei Chen ◽  
Brenda M. Molgora ◽  
Shuqi E. Wang ◽  
Augusto Simoes-Barbosa ◽  
...  

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