Formation of friable embryogenic callus in cassava is enhanced under conditions of reduced nitrate, potassium and phosphate

PLoS One. 2017 Aug 14;12(8):e0180736. doi: 10.1371/journal.pone.0180736. eCollection 2017.

Abstract

Agrobacterium-mediated transformation is an important research tool for the genetic improvement of cassava. The induction of friable embryogenic callus (FEC) is considered as a key step in cassava transformation. In the present study, the media composition was optimized for enhancing the FEC induction, and the effect of the optimized medium on gene expression was evaluated. In relative comparison to MS medium, results demonstrated that using a medium with reducing nutrition (a 10-fold less concentration of nitrogen, potassium, and phosphate), the increased amount of vitamin B1 (10 mg/L) and the use of picrolam led to reprogram non-FEC to FEC. Gene expression analyses revealed that FEC on modified media increased the expression of genes related to the regulation of polysaccharide biosynthesis and breakdown of cell wall components in comparison to FEC on normal CIM media, whereas the gene expression associated with energy flux was not dramatically altered. It is hypothesized that we reprogram non-FEC to FEC under low nitrogen, potassium and phosphate and high vitamin B1. These findings were more effective in inducing FEC formation than the previous protocol. It might contribute to development of an efficient transformation strategy in cassava.

MeSH terms

  • Culture Media
  • Gene Expression Profiling
  • Gene Expression Regulation, Plant / drug effects
  • Genes, Plant
  • Genotype
  • Manihot / drug effects
  • Manihot / embryology*
  • Manihot / genetics
  • Nitrates / pharmacology*
  • Oligonucleotide Array Sequence Analysis
  • Phosphates / pharmacology*
  • Plant Somatic Embryogenesis Techniques*
  • Plants, Genetically Modified
  • Potassium / pharmacology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Thiamine / pharmacology

Substances

  • Culture Media
  • Nitrates
  • Phosphates
  • RNA, Messenger
  • Potassium
  • Thiamine

Grants and funding

This work was supported by the following funding: 1) East Asia Science and Innovation Area Joint Research Program (e-ASIA JRP; to M.S.), Strategic Funds for the Promotion of Science and Technology (to M.S.), Core Research for Evolutionary Science and Technology (CREST Grant No.: JPMJCR13B4; to M.S.), and EIG CONCERT-Japan 4th Call under the Strategic international Research cooperative Program (to M.S.) of the Japan Science and Technology Agency (JST); 2) KAKENHI Grant Number 16K14832 (to M.S.) of the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan; 3) Science and Technology Research Partnership for Sustainable Development (SATREPS; to M.S.) of JST/Japan International Cooperation Agency (JICA); 4) Japan Society for the Promotion of Science (JSPS) Program for Advancing Strategic International Networks to Accelerate the Circulation of Talented Researchers (to M.S.); 5) RIKEN Center for Sustainable Resource Science (CSRS) (to M.S.).