The Silencing of Carotenoid β-Hydroxylases by RNA Interference in Different Maize Genetic Backgrounds Increases the β-Carotene Content of the Endosperm

Int J Mol Sci. 2017 Nov 24;18(12):2515. doi: 10.3390/ijms18122515.

Abstract

Maize (Zea mays L.) is a staple food in many parts of Africa, but the endosperm generally contains low levels of the pro-vitamin A carotenoid β-carotene, leading to vitamin A deficiency disease in populations relying on cereal-based diets. However, maize endosperm does accumulate high levels of other carotenoids, including zeaxanthin, which is derived from β-carotene via two hydroxylation reactions. Blocking these reactions could therefore improve the endosperm β-carotene content. Accordingly, we used RNA interference (RNAi) to silence the endogenous ZmBCH1 and ZmBCH2 genes, which encode two non-heme di-iron carotenoid β-hydroxylases. The genes were silenced in a range of maize genetic backgrounds by introgressing the RNAi cassette, allowing us to determine the impact of ZmBCH1/ZmBCH2 silencing in diverse hybrids. The β-carotene content of the endosperm increased substantially in all hybrids in which ZmBCH2 was silenced, regardless of whether or not ZmBCH1 was silenced simultaneously. However, the β-carotene content did not change significantly in C17 hybrids (M7 × C17 and M13 × C17) compared to C17 alone, because ZmBCH2 is already expressed at negligible levels in the C17 parent. Our data indicate that ZmBCH2 is primarily responsible for the conversion of β-carotene to zeaxanthin in maize endosperm.

Keywords: RNAi; carotenoid β-hydroxylase; hybrid; maize (Zea mays L.); β-carotene.

MeSH terms

  • Endosperm / metabolism*
  • Genotype
  • Mixed Function Oxygenases / genetics*
  • Mixed Function Oxygenases / metabolism
  • Plant Proteins / genetics*
  • Plant Proteins / metabolism
  • RNA Interference*
  • Zea mays / genetics*
  • Zea mays / metabolism
  • Zeaxanthins / metabolism
  • beta Carotene / metabolism*

Substances

  • Plant Proteins
  • Zeaxanthins
  • beta Carotene
  • Mixed Function Oxygenases
  • beta-carotene hydroxylase