The Use of CRISPR/cas9, ZFNs, TALENs in Generating Site-Specific Genome Alterations

Erscheinungsjahr 2014
ISBN: 978-0-12-801185-0
Verlag: William Andrew Publishing

Buch, Englisch, 570 Seiten, Format (B × H): 152 mm x 229 mm, Gewicht: 1100 g

This new volume of Methods in Enzymology continues the legacy of this premier serial with quality chapters authored by leaders in the field. This volume covers recent research and methods development for changing the DNA sequence within the genomes of cells and organisms. Focusing on enzymes that generate double-strand breaks in DNA, the chapters describe use of molecular tools to introduce or delete genetic information at specific sites in the genomes of animal, plant and bacterial cells.

Autoren/Hrsg.

Weitere Mitwirkende

Doudna, Jennifer A.

Fachgebiete

• Naturwissenschaften Biowissenschaften Biowissenschaften Genetik und Genomik (nichtmedizinisch)
• Naturwissenschaften Biowissenschaften Enzymologie
• Naturwissenschaften Biowissenschaften Zellbiologie
• Naturwissenschaften Biowissenschaften Bakteriologie

Inhaltsverzeichnis

1. In Vitro Enzymology of Cas9
Carolin Anders and  Martin Jinek
2. Targeted Genome Editing in Human Cells Using Crispr-Cas Nucleases and Truncated Guide Rnas
Yanfang Fu, Deepak Reyon  and J. Keith Joung
3. Determining the Specificities of Talens, Cas9, and Other Genome Editing Enzymes
Vikram Pattanayak, John P. Guilinger,and  David R. Liu
4. Genome Engineering with Custom Recombinases
Thomas Gaj, and Carlos F. Barbas
5. Genome Engineering in Human Cells
Minjung Song, Young-Hoon Kim, Hyongbum Kim1 and Jin-Soo Kim
6. Genome Editing in Human Stem Cells
Susan M. Byrne, Prashant Mali, and George M. Church
7. Tagging Endogenous Loci for Live-Cell Fluorescence Imaging and Molecule Counting Using ZFNs, Talens and Cas9
Dambournet D., Hong SH., Grassart A and  Drubin DG
8. Genome Editing Using Cas9 Nickases
Alexandro E. Trevino and Feng Zhang
9. Assaying Break and Nick-Induced Homologous Recombination in Mammalian Cells Using the DR-GFP Reporter and Cas9 Nucleases
Lianne E.M. Vriend, Maria Jasin and Przemek M. Krawczyk
10. Adapting CRISPR/Cas9 for Functional Genomics Screens
Abba Malina, Alexandra Katigbak, Regina Cencic, Rayelle Itoua Maïga, Francis Robert, Hisashi Miura and Jerry Pelletier
11.  The iCRISPR Platform for Rapid Genome Editing in Human Pluripotent Stem Cells
Zengrong Zhu, Federico González and  Danwei Huangfu
12. Creating Cancer Translocations in Human Cells Using Cas9 DSBs and nCas9 Paired Nicks
Benjamin Renouf, Marion Piganeau, Hind Ghezraoui, Maria Jasin and Erika Brunet
13. Genome Editing for Human Gene Therapy
Torsten B. Meissner, Pankaj K. Mandal, Leonardo M. R. Ferreira, Derrick J. Rossi and Chad A. Cowa
14. Generation of Site-Specific Mutations in the Rat Genome Via CRISPR-Cas9
Yuting Guan, Yanjiao Shao, Dali Li  and Mingyao Liu
15. CRISPR-Cas9-Based Genome Editing in Mice by Single Plasmid Injection
Yoshitaka Fujihara and Masahito Ikawa
16. Imaging Genomic Elements in Living Cells using CRISPR/Cas9
Baohui Chen and Bo Huang
17. Cas9-Based Genome Editing in Xenopus Tropicalis
Takuya Nakayama, Ira L. Blitz, Margaret B. Fish, Akinleye O. Odeleye, Sumanth Manohar, Ken W.Y. Cho and Robert M. Grainger
18. Cas9-Based Genome Editing in Zebrafish
Andrew P.W. Gonzales, and Jing-Ruey Joanna Yeh
19. Cas9-Based Genome Editing in Drosophila
Benjamin E. Housden, Shuailiang Lin  and  Norbert Perrimon
20. Transgene Free Genome Editing by Germline Injection of CRISPR Cas RNA
Hillel T Schwartz and Paul W Sternberg
21. Cas9-Based Genome Editing in Arabidopsis and Tobacco
Jian-Feng Li, Dandan Zhang, and Jen Sheen
22. Multiplex Engineering of Industrial Yeast Genomes Using CRISPRm
Owen W. Ryan1 and Jamie H. D. Cate
23. Protein Engineering of Cas9 for Enhanced Function
Benjamin L. Oakes, Dana C. Nadler, and David F. Savage

Über Autor(innen)

Doudna, Jennifer A.
Jennifer A. Doudna, Ph.D., professor of Molecular and Cell Biology and Chemistry at the University of California, Berkeley and Howard Hughes Medical Institute investigator, has devoted her scientific career to revealing the secret life of RNA. Using the approaches of structural biology and biochemistry, Doudna's work deciphering the molecular structure of RNA enzymes and other functional RNAs has shown how these seemingly simple molecules can carry out complex functions and can work together with proteins to control the information content of a cell.

Doudna grew up amidst the natural wonders of Hawaii, where she experienced volcanic eruptions, explored remote beaches and honed her body-surfing skills while living in the small town of Hilo on the Big Island. Doudna earned a B.A. in Biochemistry at Pomona College in 1985, where she worked with outstanding chemists Sharon Panasenko and Fred Grieman, and enjoyed the mentorship of many other great professors. She then worked with Jack Szostak at Harvard, completing her Ph.D. in 1989 on the develpoment of a self-replicating RNA based on the activity of a group I self-splicing intron. This work showed how RNA could function as both a template and a catalyst for generating copies of itself, a key propoerty of life. As a Lucille Markey postdoctoral associate with Tom Cech at University of Colorado at Boulder, Doudna began crystallizing catalytic RNA molecules with a goal of determining their three-dimensioanl structures and hence inlocking the key to their biochemical activities. She continued this work as a faculty member at Yale University, where she became a professor in 1994 in the Department of Molecular Biophysics and Biochemistry. In two landmark studies early in her career, Doudna and colleagues solved the crystal structures of two large RNAs - the P4-P6 domain of the Tetrahymena thermophila group I intron ribozyme and the hepatitis delta virus ribozyme. By determining their molecular structures, her work advanced the understanding of RNA's ability to function as a catalyst in biological systems. In 2002, Doudna moved to the University of California at Berkeley, where her lab began studying the function of small RNAs that control the use of a cell's genetic information. This led to her work on bacterial immune systems that employ RNA molecules derived from viruses to target and destroy foreign DNA. In collaboration with the lab of Emmanuelle Charpentier, Doudna and postdoctoral associate Martin Jinek discovered the function of an RNA-guided enzyme in the bacterial immune pathway, Cas9, whose ability to cut double-stranded DNA can be programmed by changing the guide RNA sequence. They recognized that such an activity could be employed as a molecular tool for precision genome engineering in various kinds of cells, a discovery that has triggered a revolution in the fields of molecular genetics and genomics.

Doudna's work has been honored by numerous awards. She received the National Academy of Sciences Award for Initiatives in Research in 1999, and the Alan T. Waterman Award from the NSF in 2000. In 2001 she received the Eli Lilley Award in Biological Chemistry from the American Chemical Society, and in 2013 she was the recipient of the Mildred Cohn Award from ASBMB and the Hans Neurath Award from the Protein Society. She has been a Howard Hughes Medical Institute investigator since 1997 and a member of the National Academy of Sciences since 2002. She was named to the American Academy of Arts and Sciences in 2003 and elected to the Institute of Medicine in 2010. In 2014 she received the Lurie Prize from the Foundation for the NIH.