Identification of MeC3HDZ1/MeCNA as a potential regulator of cassava storage root development.

Plant Sci

Institute for Plant Molecular and Cell Biology (IBMCP), CSIC-Universitat Politècnica de Valencia, Camino de Vera S/N, 46022 València, Spain. Electronic address:

Published: February 2024

AI Article Synopsis

  • Cassava's storage root is a vital food source for over 500 million people in sub-Saharan Africa, and understanding its genetic regulation is crucial for biotechnological improvements.
  • Researchers identified eight C3HDZ transcription factors in cassava, focusing particularly on MeC3HDZ1, which shows high expression in the storage root cambium and xylem.
  • MeC3HDZ1 is confirmed to regulate gene expression related to storage root development, suggesting it could be a key target for enhancing cassava productivity in future biotechnological applications.

Article Abstract

The storage root (SR) of cassava is the main staple food in sub-Saharan Africa, where it feeds over 500 million people. However, little is known about the genetic and molecular regulation underlying its development. Unraveling such regulation would pave the way for biotechnology approaches aimed at enhancing cassava productivity. Anatomical studies indicate that SR development relies on the massive accumulation of xylem parenchyma, a cell-type derived from the vascular cambium. The C3HDZ family of transcription factors regulate cambial cells proliferation and xylem differentiation in Arabidopsis and other species. We thus aimed at identifying C3HDZ proteins in cassava and determining whether any of them shows preferential activity in the SR cambium and/or xylem. Using phylogeny and synteny studies, we identified eight C3HDZ proteins in cassava, namely MeCH3DZ1-8. We observed that MeC3HDZ1 is the MeC3HDZ gene displaying the highest expression in SR and that, within that organ, the gene also shows high expression in cambium and xylem. In-silico analyses revealed the existence of a number of potential C3HDZ targets displaying significant preferential expression in the SR. Subsequent Y1H analyses proved that MeC3HDZ1 can bind canonical C3HDZ binding sites, present in the promoters of these targets. Transactivation assays demonstrated that MeC3HDZ1 can regulate the expression of genes downstream of promoters harboring such binding sites, thereby demonstrating that MeC3HDZ1 has C3HDZ transcription factor activity. We conclude that MeC3HDZ1 may be a key factor for the regulation of storage root development in cassava, holding thus great promise for future biotechnology applications.

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http://dx.doi.org/10.1016/j.plantsci.2023.111938DOI Listing

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