Decoding and recoding plant development

Plant Physiol. 2021 Oct 5;187(2):515-526. doi: 10.1093/plphys/kiab336.

Abstract

The development of multicellular organisms has been studied for centuries, yet many critical events and mechanisms of regulation remain challenging to observe directly. Early research focused on detailed observational and comparative studies. Molecular biology has generated insights into regulatory mechanisms, but only for a limited number of species. Now, synthetic biology is bringing these two approaches together, and by adding the possibility of sculpting novel morphologies, opening another path to understanding biology. Here, we review a variety of recently invented techniques that use CRISPR/Cas9 and phage integrases to trace the differentiation of cells over various timescales, as well as to decode the molecular states of cells in high spatiotemporal resolution. Most of these tools have been implemented in animals. The time is ripe for plant biologists to adopt and expand these approaches. Here, we describe how these tools could be used to monitor development in diverse plant species, as well as how they could guide efforts to recode programs of interest.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • CRISPR-Cas Systems / genetics
  • Cell Differentiation*
  • Cell Lineage*
  • Gene Editing*
  • Genetic Engineering
  • Integrases / genetics
  • Molecular Biology
  • Plant Development / genetics
  • Plant Development / physiology*
  • Synthetic Biology*
  • Systems Biology*

Substances

  • Integrases