TY  - JA
AU  - Liu,L.
AU  - Zhang Yudong
AU  - Meiling Ding
AU  - Wei Chen
AU  - Kang,M.S.
AU  - Fan Xingming
AU  - Jeffers,D.P.
TI  - Introgression of the crtRB1 gene into quality protein maize inbred lines using molecular markers
PY  - 2015///
CY  - Dordrecht (Netherlands) : 
PB  - Springer
KW  - Retinol
KW  - AGROVOC
KW  - Inbred lines
KW  - Maize
N1  - Peer review; Open Access
N2  - Quality protein maize (QPM; Zea mays L.) has effectively enhanced levels of the amino acids, lysine, and tryptophan, over normal maize and provided balanced dietary protein for the health and development of monogastric animals and humans. However, as in normal maize, QPM varieties are low in provitamin A (ProVA), a precursor of vitamin A, which can lead to vitamin A deficiency in humans when maize is a significant part of their diet. In this study, maize inbred Hp321-1 carrying the favorable alleles crtRB1-50 TE-2 and crtRB1-30 TE-1 that can enhance levels of ProVA, was used as donor for improving ProVA in QPM inbred lines CML161 and CML171. Functional markers for identifying the favorable alleles crtRB1-50 TE-2 and crtRB1-30 TE-1 were used in foreground selection, and simple sequence repeat markers were used in background selection for the BC1F1, BC2F1, and BC2F2 generations. The background recovery rates were 77.4 and 84.5 % for CML161 and CML171 populations, respectively, in the BC1F1 generation, and 89.9 and 92.1 % in the BC2F2 generation. With foreground and background selection, the mean ProVA concentration has been improved from 1.60 lg g-1 in the parent of CML161 to 5.25 lg g-1 in its BC2F3 offspring, from 1.80 lg g-1 in the parent of CML171 to 8.14 lg g-1 in its BC2F3 offspring while maintaining similar QPM characteristics of the recurrent parents. The success from this study offers maize breeders a procedure for increasing ProVA in QPM lines, which will greatly mitigate vitamin A defi- ciency and protein-energy malnutrition in developing countries
UR  - https://hdl.handle.net/10883/19751
T2  - Molecular Breeding
DO  - https://doi.org/10.1007/s11032-015-0349-7
ER  -