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The University of Southampton
Biological Sciences

Synthetic genetics: beyond DNA and RNA Event

Research talk
Time:
13:00
Date:
7 March 2018
Venue:
Building 5, Room 2017, Lecture Theatre J, Highfield Campus

For more information regarding this event, please telephone Selina Barry on 023 80 59 4794 or email S.J.Barry@soton.ac.uk .

Event details

Biological Sciences Invited Speaker Programme 2017-18

Abstract: Synthetic biology seeks to probe fundamental aspects of biological form and function by construction (i.e. resynthesis) rather than deconstruction (analysis). Synthesis thus complements reductionist and analytic studies of life, and allows novel approaches towards fundamental biological questions.  We have been exploiting the synthesis paradigm to explore the chemical etiology of the genetic apparatus shared by all life on earth. Specifically, we ask why information storage and propagation in biological systems is based on just two types of nucleic acids, DNA and RNA. Is the chemistry of life’s genetic system based on chance or necessity? Does it reflect a "frozen accident", imposed at the origin of life, or are DNA and RNA functionally superior to simple alternatives. I’ll be presenting recent progress on the development and application of strategies to enable the enzymatic synthesis and reverse transcription and hence replication and evolution of novel synthetic genetic polymers, which we term XNAs. We show that eight different synthetic polymers, based on nucleic acid architectures not found in nature, can also mediate genetic information storage and propagation [1]. Beyond heredity, we demonstrate a capacity for Darwinian evolution by the de novo selection of specific ligands (XNA aptamers) and catalysts (XNAzymes) based on entirely synthetic backbones [1, 2]. Thus, key hallmarks of living systems, including heredity and evolution are not limited to DNA and RNA but can be implemented in synthetic polymers and are likely to be emergent properties of polymers capable of information storage.

Speaker information

Dr Philipp Holliger,University of Cambridge, the MRC Laboratory of Molecular Biology (LMB)

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