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Targeted Modification
of Genomes with Lactococcus Lactis Ll.LtrB Group II Intron
(TARGETRON)
Introduction
Functional genomic disciplines seek to
understand the contributions of genes and their protein products
in healthy and disease conditions. Due to evolutionary conservation,
model organisms provide simplified systems for analysis, while
still producing relevant results. Gene function can be assessed
by two principal methods: gain of function and loss of function
methodologies. Gain of function approaches seek to express
novel genes in organisms or overexpress the corresponding
gene in a model organism. Loss of function approaches focus
on gene disruption. In both approaches, the physiologic consequences
of the gene manipulation is measured. Yeast represents a favored
eukaryotic genetic system. The group II intron LtrB is a ribozyme
that catalyzes its own splicing and is able to insert itself
into essentially any gene in various species. In order to
use group II introns to manipulate eukaryotic genomes, the
catalytically active ribonucleoprotein (RNP) particles must
be expressed. Manners to apply these technologies in eukaryotic
cells are limited.
Invention Description
Our invention enables high-throughput
screening of genomes for the purpose of targeted modifications
of DNA with the LI.LtrB group II intron (targetron). A computer
algorithm identifies suitable targets for a specific, regulatable
chromosomal gene delivery or for desired gene disruption.
The algorithm design tailors targetrons for genetic engineering,
functional genomics, and potential gene therapy in living
organisms, including mammalian cells, yeast, zebrafish, and
oocyte nuclei.
Benefits
- Targeted and efficient modification
of genomes
- Does not require the use of antiobiotic-resistance
gene as a selection marker
Features
- Computer algorithm using LI.LtrB group
II intron for target identification
IP Status
Copyrighted method
UT Researcher
Alan Lambowitz, Ph.D., Institute
for Cellular and Molecular Biology, The University of Texas
at Austin
Jiri Perutka, Ph.D., Institute for Cellular and Molecular
Biology, The University of Texas at Austin
For further information please contact:
University of Texas,
Austin, USA
Website : www.otc.utexas.edu

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