Akanksha Thawani, PhD

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Overview

Dr. Akanksha Thawani is an Assistant Professor in the Department of Biochemistry and Molecular Biophysics at Columbia University Irving Medical Center. She earned her B.Tech. in Chemical Engineering and Computer Science from the Indian Institute of Technology Bombay, graduating with the Institute Silver Medal and the highest cumulative GPA in her class. She completed her Ph.D. in Chemical and Biological Engineering at Princeton University, where she trained with Dr. Sabine Petry, Dr. Howard A Stone and Dr. Josh Shaevitz. Her doctoral work uncovered design principles of microtubule nucleation and mitotic spindle assembly, including a core microtubule nucleation module and regulatory mechanisms that enable robust yet adaptable cytoskeletal self-organization.

Akanksha carried this mechanistic mindset into genome biology during her postdoctoral training at the University of California, Berkeley, where she was a Damon Runyon Cancer Research Fellow in the laboratories of Eva Nogales and Kathleen Collins. There, she pioneered biochemical reconstitution and cryo-electron microscopy approaches to capture mobile genetic elements in the human genome, producing the first atomic-resolution structures of the human LINE-1 retrotransposon machinery engaged with its native RNA and DNA substrates. Her work revealed how LINE elements hijack human DNA replication and demonstrated how retrotransposon mechanisms can be repurposed for efficient, RNA-only genome insertion without double-strand breaks. She also helped establish the structural and mechanistic basis for R2 retrotransposon insertion and contributed to the development of targeted, donor-free transgene insertion strategies at the human rDNA locus.

At Columbia, the Thawani Laboratory investigates how mobile elements shape genomes across the tree of life and how their mechanisms can be harnessed for biotechnology. The lab integrates structural biology, biochemistry, functional genomics, and genome engineering to illuminate retrotransposon biology in health and disease while developing next-generation genome-writing technologies. Dr. Thawani is committed to rigorous and supportive mentorship. Her work and mentoring have been recognized through major early-career support, including a Burroughs Wellcome Fund Career Award at the Scientific Interface and the Damon Runyon Dale F. Frey Award for Breakthrough Scientists.

Credentials & Experience

Education & Training

  • BA, 2014 Chemical Engineering and Computer Science, Indian Institute of Technology (IIT) Bombay
  • PhD, 2020 Chemical and Biological Engineering, Princeton University
  • Fellowship: 2025 Molecular Biology, University of California, Berkeley

Honors & Awards

  • 2025: Burroughs Wellcome Fund Career Award at the Scientific Interface
  • 2025: Damon Runyon Dale F. Frey Award
  • 2024: STAT Wunderkind
  • 2024: MIT Technology Review 35 Under 35 Innovators (regional)
  • 2024: Eddie Méndez Award, Fred Hutchinson Cancer Center
  • 2023: Leading Edge Fellow
  • 2021: Damon Runyon Cancer Research Foundation Postdoctoral Fellowship
  • 2020: Harold M. Weintraub Graduate Student Award

Research

Decoding and harnessing mobile genetic elements

Eukaryotic cells face a central tension: they must preserve genome integrity across cell divisions while continually confronting, and often co-opting, mobile genetic elements that can rewrite DNA. Among the most powerful of these are retrotransposons, RNA-guided ‘copy-and-paste’ systems that have shaped genome architecture over millions of years and remain active in humans. LINE-1, the only autonomously active retrotransposon in the human genome, is a major driver of somatic variation and is increasingly linked to genome instability and inflammatory signaling in cancer, neurodegeneration, and aging. At the same time, retrotransposons execute efficient genome insertion without donor DNA or double-strand breaks, offering a blueprint for safer large-payload gene insertion technologies.

The Thawani Lab seeks to define, at molecular resolution, how retrotransposon machines assemble, recognize nucleic acid substrates, recruit host DNA replication and repair pathways, and complete genome insertion. We combine biochemical reconstitution, high-resolution cryo-electron microscopy, functional genomics, and long-read sequencing to capture insertion intermediates and map host-factor dependencies across cellular contexts. In parallel, we translate mechanistic insight into engineering: repurposing LINE-like and R2 retrotransposon systems for RNA-only, donor-free transgene insertion and developing strategies to improve specificity, fidelity, and control. By uniting fundamental mechanism with tool development, our goal is to reveal how the “dark matter” of the genome influences human physiology and disease, and to convert nature’s genome-writing enzymes into next-generation platforms for therapeutic genome engineering.

Please visit the Thawani Lab for more information.

Selected Publications

  1. Thawani A*, Rodriguez-Vargas AJ*, Treeck BV, Hassan NT, Aledson D, Nogales E, Collins K. Structures of vertebrate R2 retrotransposon complexes during target-primed reverse transcription and after second strand nicking. Science Advances, 11, 10.1126/sciadv.adu5533 (2025).
  2. Thawani A, Collins K, Nogales E. Structural and biochemical studies of mobile retrotransposon proteins in action. Current Opinion in Structural Biology, 92, 103053 (2025).
  3. Thawani A, Florez Ariza AJ, Nogales E, Collins K. Template and target-site recognition by human LINE-1 in retrotransposition. Nature 626, 186-193 (2024).
  4. Thawani A, Petry S. Molecular insight into how the 𝛾-Tubulin Ring Complex makes microtubules. Journal of Cell Science 134, 14, jcs245464 (2021).
  5. Thawani A, Rale MJ, Coudray N, Bhabha G, Shaevitz JW, Stone HA, Petry S. The transition state and regulation of 𝛾-TuRC-mediated microtubule nucleation revealed by single molecule microscopy. eLife, doi.org/10.7554/eLife.54253 2020 (2020).
  6. Thawani A, Stone HA, Shaevitz JW, Petry S. Spatiotemporal organization of branched microtubule networks eLife, doi.org/10.7554/eLife.43890 (2019).
  7. Thawani A*, Kadzik RS*, Petry S. XMAP215 is a microtubule nucleation factor that functions synergistically with the gamma-tubulin ring complex. Nature Cell Biology, 20, 575–585 (2018).