Iron(Fe) is an essential micronutrient required by all fruit trees. To elucidate the regulatory mechanism of auxin to the long-distance transport of Fe, a gene encoding a putative CS protein was isolated from Pyrus be...Iron(Fe) is an essential micronutrient required by all fruit trees. To elucidate the regulatory mechanism of auxin to the long-distance transport of Fe, a gene encoding a putative CS protein was isolated from Pyrus betulifolia. This gene was designated as Pb CS1 containing 1 422 bp in length with an open reading frame encoding a protein of 473 amino acids with a predicted molecular mass of 52.69 ku and a theoretical isoelectric point of 6.91. The deduced Pb CS1 protein contained a conserved CS domain and WPNVDAHS sequence existing in the PWPN-box. Based on its conserved domain and phylogenetic status, the Pb CS1 should be grouped into type-Ⅰ subfamily of plant CS. Quantitative real-time PCR results indicated that the Pb CS1 expression was enriched in leaves, roots and phloem, but relatively weak in xylem. Using split root systems, Fe deficiency in one portion of the root system could induce dramatic up-regulation of the Pb CS1 expression in the Fe-sufficient part, suggesting that the Pb CS1 expression was activated by systemic signals. In addition, supplying with NAA and exogenous auxin to the de-topped shoots could recover the Fe deficiency-induced up-regulation of the Pb CS1 expression in the Fe-sufficient part of the root system. In contrast, NPA(an auxin transport inhibitor) application to the shoot tips arrested up-regulation of the Pb CS1 expression in the untreated portion. The results suggested that Fe-deficiency-induced alterations of the Pb CS1 expression were mediated by auxin.展开更多
基金financial support from China Agriculture Research System (CARS-29-13)
文摘Iron(Fe) is an essential micronutrient required by all fruit trees. To elucidate the regulatory mechanism of auxin to the long-distance transport of Fe, a gene encoding a putative CS protein was isolated from Pyrus betulifolia. This gene was designated as Pb CS1 containing 1 422 bp in length with an open reading frame encoding a protein of 473 amino acids with a predicted molecular mass of 52.69 ku and a theoretical isoelectric point of 6.91. The deduced Pb CS1 protein contained a conserved CS domain and WPNVDAHS sequence existing in the PWPN-box. Based on its conserved domain and phylogenetic status, the Pb CS1 should be grouped into type-Ⅰ subfamily of plant CS. Quantitative real-time PCR results indicated that the Pb CS1 expression was enriched in leaves, roots and phloem, but relatively weak in xylem. Using split root systems, Fe deficiency in one portion of the root system could induce dramatic up-regulation of the Pb CS1 expression in the Fe-sufficient part, suggesting that the Pb CS1 expression was activated by systemic signals. In addition, supplying with NAA and exogenous auxin to the de-topped shoots could recover the Fe deficiency-induced up-regulation of the Pb CS1 expression in the Fe-sufficient part of the root system. In contrast, NPA(an auxin transport inhibitor) application to the shoot tips arrested up-regulation of the Pb CS1 expression in the untreated portion. The results suggested that Fe-deficiency-induced alterations of the Pb CS1 expression were mediated by auxin.
