TY - CHAP
T1 - CRISPR based development of RNA editing and the diagnostic platform
AU - Satish, Lakkakula
AU - Lavanya, Gunamalai
AU - Kasthuri, Thirupathi
AU - Kalaivaani, Aruchamy
AU - Shamili, Sasanala
AU - Muthuramalingam, Pandiyan
AU - Gowrishankar, Shanmugaraj
AU - Pandian, Shunmugiah Karutha
AU - Singh, Vijai
AU - Sitrit, Yaron
AU - Kushmaro, Ariel
N1 - Publisher Copyright: © 2021 Elsevier Inc.
PY - 2021/1/1
Y1 - 2021/1/1
N2 - Clustered Regularly Interspersed Short Palindromic Repeat-CRISPR-Associated (CRISPR-Cas) system has improved the ability to edit and control gene expression as desired. Genome editing approaches are currently leading the biomedical research with improved focus on direct nuclease dependent editing. So far, the research was predominantly intended on genome editing over the DNA level, recent adapted techniques are initiating to secure momentum through their proficiency to provoke modifications in RNA sequence. Integration of this system besides to lateral flow method allows reliable, quick, sensitive, precise and inexpensive diagnostic. These interesting methods illustrate only a small proportion of what is technically possible for this novel technology, but several technological obstacles need to be overcome prior to the CRISPR-Cas genome editing system can meet its full ability. This chapter covers the particulars on recent advances in CRISPR-Cas9 genome editing technology including diagnosis and technical advancements, followed by molecular mechanism of CRISPR-based RNA editing and diagnostic tools and types, and CRISPR-Cas-based biosensors.
AB - Clustered Regularly Interspersed Short Palindromic Repeat-CRISPR-Associated (CRISPR-Cas) system has improved the ability to edit and control gene expression as desired. Genome editing approaches are currently leading the biomedical research with improved focus on direct nuclease dependent editing. So far, the research was predominantly intended on genome editing over the DNA level, recent adapted techniques are initiating to secure momentum through their proficiency to provoke modifications in RNA sequence. Integration of this system besides to lateral flow method allows reliable, quick, sensitive, precise and inexpensive diagnostic. These interesting methods illustrate only a small proportion of what is technically possible for this novel technology, but several technological obstacles need to be overcome prior to the CRISPR-Cas genome editing system can meet its full ability. This chapter covers the particulars on recent advances in CRISPR-Cas9 genome editing technology including diagnosis and technical advancements, followed by molecular mechanism of CRISPR-based RNA editing and diagnostic tools and types, and CRISPR-Cas-based biosensors.
KW - Biosensors
KW - CRISPR-Cas system
KW - Genome editing
KW - Non-coding RNA
KW - Targeted gene repair
UR - http://www.scopus.com/inward/record.url?scp=85101327950&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/bs.pmbts.2020.12.015
DO - https://doi.org/10.1016/bs.pmbts.2020.12.015
M3 - Chapter
C2 - 33785175
SN - 9780323853217
T3 - Progress in Molecular Biology and Translational Science
SP - 117
EP - 159
BT - Reprogramming the Genome
A2 - Singh, Vijai
PB - Elsevier B.V.
ER -