Crisanti:Andrew M Hammond: Difference between revisions
| Line 21: | Line 21: | ||
==Research interests== | ==Research interests== | ||
<!-- Feel free to add brief descriptions to your research interests as well --> | <!-- Feel free to add brief descriptions to your research interests as well --> | ||
I am a PhD student in Crisanti | I am a PhD student in [[Crisanti:Crisanti Lab | Crisanti Lab]] at [http://www.imperial.ac.uk/ Imperial College], working towards the development of a synthetic gene drive strategy for population suppression in malaria mosquitoes. As a lab, we are investigating the use of HEGs, TALENs and CRISPR as a homing endonuclease to invade and subsequently supress mosquito populations – as initially theorised by the principal investigator, Professor Austin Burt. | ||
My work is focused upon CRISPR, validating it as a tool for genome engineering in mosquitoes and testing the potential to use it in a gene drive. Previous research has predicted that an endonuclease-based gene drive targeting a female fertility gene would efficiently suppress populations if the mutations to this gene result in a recessive sterile phenotype. | My work is focused upon CRISPR, validating it as a tool for genome engineering in mosquitoes and testing the potential to use it in a gene drive. Previous research has predicted that an endonuclease-based gene drive targeting a female fertility gene would efficiently suppress populations if the mutations to this gene result in a recessive sterile phenotype. | ||
Revision as of 08:03, 5 May 2015
Contact Info
Andrew M Hammond
Crisanti lab
Division of Cell & Molecular Biology
South Kensington Campus, SAF
London, SW72AZ
UK
mail: andrew.hammond08[ät]imperial.ac.uk
Education
- 2012 - Present, PhD, Imperial College London
- 2011, BSc, Imperial College London
Research interests
I am a PhD student in Crisanti Lab at Imperial College, working towards the development of a synthetic gene drive strategy for population suppression in malaria mosquitoes. As a lab, we are investigating the use of HEGs, TALENs and CRISPR as a homing endonuclease to invade and subsequently supress mosquito populations – as initially theorised by the principal investigator, Professor Austin Burt.
My work is focused upon CRISPR, validating it as a tool for genome engineering in mosquitoes and testing the potential to use it in a gene drive. Previous research has predicted that an endonuclease-based gene drive targeting a female fertility gene would efficiently suppress populations if the mutations to this gene result in a recessive sterile phenotype.
We have made great steps towards achieving this ambitious aim, including the first use of CRISPR in Anopheles gambiae mosquitoes. To date, we have used CRISPR to characterise in vivo a number of recessive female sterile genes - demonstrating a high level of CRISPR activity in the process. Early results suggest that we can precisely engineer the genome of mosquitoes using CRISPR and that the technology meets all of the requirements for use a population suppressor.
Publications
- Goldbeter A and Koshland DE Jr. An amplified sensitivity arising from covalent modification in biological systems. Proc Natl Acad Sci U S A. 1981 Nov;78(11):6840-4. DOI:10.1073/pnas.78.11.6840 |
- JACOB F and MONOD J. Genetic regulatory mechanisms in the synthesis of proteins. J Mol Biol. 1961 Jun;3:318-56. DOI:10.1016/s0022-2836(61)80072-7 |
leave a comment about a paper here
- ISBN:0879697164
Useful links
