Aashiq H. Kachroo, PhD.
Assistant Professor, Center for Applied Synthetic Biology, Biology
Canada Research Chair Tier 2 in Systems & Synthetic Biology, Biology
Biography Teaching activities Research activities Publications Participation activities Research & Infrastructure funding

Phone: | (514) 848-2424 ext. 2493 |
Email: | aashiq.kachroo@concordia.ca |
Website(s): |
Laboratory web page |
Availability: |
Lab - GE 320.01 Lab Phone 514-848-2424 ext. 5977 |
Education
PhD (Indian Institute of Science, Bangalore, INDIA)
PDF (The University of Texas at Austin, Austin, TX, USA)
Teaching activities
BIOL367-Fall
Molecular Biology
BIOL485/523/632-Winter
Agriculture & Agri-Food Biotechnology/ Advanced Biotechnology
Research activities
Engineering complex biological processes in simplified cells
The most deeply evolutionarily conserved human genes encode essential cellular machinery whose failures are linked to diverse diseases, from cancer to cardiovascular disease. Recent systematic studies have discovered extensive genetic polymorphism in these genes yet studying how these variations contribute to cellular function and overall human health remains a challenge. Our group is interested in studying these conserved human genes along with many of their variants, by systematically humanizing yeast cells, replacing each of the essential yeast genes in turn by its human version. The resulting strains will serve as new physical reagents for studying the human genes in a simplified organismal context, opening up simple high-throughput assays of human gene function, analyzing the impact of human genetic variation on gene function, the screening and repurposing of drugs and the rapid determination of mechanisms of drug resistance. Our work will illuminate fundamental principles of evolution, providing direct measurements of whether or not human and yeast genes have retained their ancestral functions over a billion years of evolutionary divergence.

Photo credit: Aashiq H. Kachroo
Publications
- SELECT PUBLICATIONS
- * Equal author
- & Corresponding author
- Pre-print
- 1. Garge RK*, Cha HJ*, Lee C, Gollihar JD, Kachroo AH, Wallingford JB&, Marcotte EM&. Antifungal benzimidazoles disrupt vasculature by targeting one of nine beta-tubulins. bioRxiv. 2020 (link)
Peer-reviewed
- 1. Garge RK, Laurent JM, Kachroo AH&, Marcotte EM&. Systematic humanization of the yeast cytoskeleton discerns functionally replaceable from divergent human genes. Genetics. 2020; PMID: 32522745 (link)
2. Laurent JM, Garge RK, Teufel AI, Wilke CO, Kachroo AH&, Marcotte EM&. Humanization of yeast genes with multiple human orthologs reveals functional divergence between paralogs. PLoS Biology. 2020; PMID:32421706. (link)
3. Teufel AI, Johnson MM, Laurent JM, Kachroo AH, Marcotte EM, Wilke CO. The many nuanced evolutionary consequences of duplicated genes. Molecular Biology and Evolution. 2019; PMID: 30428072.
4. Akhmetov A, Laurent JM, Gollihar J, Gardner EC, Garge RK, Ellington AD, Kachroo AH&, Marcotte EM&. Single-step Precision Genome Editing in Yeast Using CRISPR-Cas9. Bio-protocol. 2018; PMID: 29770349. (link)
5. Kachroo AH*&, Laurent JM*, Akhmetov A, Szilagyi-Jones M, McWhite CD, Zhao A,Marcotte EM&. Systematic bacterialization of yeast genes identifies a near-universally swappable pathway. eLife. 2017 Jun 29;6. pii: e25093. doi: 10.7554/eLife.25093. PMID: 28661399. (link)
6. Laurent JM, Young JH, Kachroo AH, Marcotte EM. Efforts to make and apply humanized yeast. Brief Funct Genomics. 2016, PMID: 26462863. (link)
7. Cannon B*, Kachroo AH*, Jarmoskaite I, Jayaram M, Russell R. Hexapeptides that inhibit processing of branched DNA structures induce a dynamic ensemble of Holliday junction conformations. J Biol Chem. 2015 Sep 11;290(37):22734-46. PMID: 26209636;PMCID: PMC4566245. (link)
8. Kachroo AH, Laurent JM, Yellman CM, Meyer AG, Wilke CO, Marcotte EM&. Evolution. Systematic humanization of yeast genes reveals conserved functions and genetic modularity. Science. 2015 May 22;348(6237):921-5. PMID: 25999509; PMCID: PMC4718922. (link)
9. Rowley PA*, Kachroo AH*, Ma CH, Maciaszek AD, Guga P, Jayaram M. Stereospecific suppression of active site mutants by methylphosphonate substituted substrates reveals the stereochemical course of site-specific DNA recombination. Nucleic Acids Res. 2015 Jul 13;43(12):6023-37. PMID: 25999343; PMCID: PMC4499138. (link)
Participation activities
Undergraduate mentorship
Concordia University-iGEM supervisor
2018-present
2019- Gold Medal at iGEM 2019 & nomination for the Best Presentation
2020- Gold Medal at iGEM 2020 & Best Software Award
Research & Infrastructure funding
NSERC-Discovery; NSERC-CREATE; FRQNT; CFI; CRC