000 03535nab a22004097a 4500
999 _c56864
_d56856
001 56864
003 MX-TxCIM
005 20211006085122.0
007 ta
008 150424s2015 xxu|||p|op||| 00| 0 eng d
024 8 _ahttps://doi.org/10.1007/s00122-015-2475-3
040 _aMX-TxCIM
041 _aeng
100 1 _aSuwarno, W.B.
_9714
245 1 0 _aGenome‑wide association analysis reveals new targets for carotenoid biofortification in maize
260 _aNew York:
_bSpringer,
_c2015.
500 _aPeer review
500 _aOpen Access
520 _aKey message Genome-wide association analysis in CIMMYT’s association panel revealed new favorable native genomic variations in/nearby important genes such as hydroxylases and CCD1 that have potential for carotenoid biofortification in maize. Abstract Genome-wide association studies (GWAS) have been used extensively to identify allelic variation for genes controlling important agronomic and nutritional traits in plants. Provitamin A (proVA) enhancing alleles of lycopene epsilon cyclase (LCYE) and β-carotene hydroxylase 1 (CRTRB1), previously identified through candidate-gene based GWAS, are currently used in CIMMYT’s maize breeding program. The objective of this study was to identify genes or genomic regions controlling variation for carotenoid concentrations in grain for CIMMYT’s carotenoid association mapping panel of 380 inbred maize lines, using high-density genome-wide platforms with ~476,000 SNP markers. Population structure effects were minimized by adjustments using principal components and kinship matrix with mixed models. Genome-wide linkage disequilibrium (LD) analysis indicated faster LD decay (3.9 kb; r2 = 0.1) than commonly reported for temperate germplasm, and therefore the possibility of achieving higher mapping resolution with our mostly tropical diversity panel. GWAS for various carotenoids identified CRTRB1, LCYE and other key genes or genomic regions that govern rate-critical steps in the upstream pathway, such as DXS1, GGPS1, and GGPS2 that are known to play important roles in the accumulation of precursor isoprenoids as well as downstream genes HYD5, CCD1, and ZEP1, which are involved in hydroxylation and carotenoid degradation. SNPs at or near all of these regions were identified and may be useful target regions for carotenoid biofortification breeding efforts in maize; for example a genomic region on chromosome 2 explained ~16 % of the phenotypic variance for β-carotene independently of CRTRB1, and a variant of CCD1 that resulted in reduced β-cryptoxanthin degradation was found in lines that have previously been observed to have low proVA degradation rates.
536 _aGlobal Maize Program
536 _aGenetic Resources Program
546 _aText in english
591 _bCIMMYT Informa No. 1932
594 _aINT1617
594 _aINT2691
594 _aINT2925
650 7 _aMaize
_gAGROVOC
_2
_91173
650 7 _91032
_aCarotenoids
_gAGROVOC
650 7 _91132
_aGenomics
_2AGROVOC
700 1 _9143
_aKaeppler, S.M.
700 1 _9832
_aPixley, K.V.
_gGenetic Resources Program
_8INT1617
700 1 _9850
_aPalacios-Rojas, N.
_gGlobal Maize Program
_8INT2691
700 1 _9875
_aBABU, R.
_gGlobal Maize Program
_8INT2925
773 0 _wu444762
_x1432-2242 (Revista en electrónico)
_dBerlin (Germany) : Springer-Verlag Heidelberg
_tTheoretical and Applied Genetics
_gv. 128, no. 2
856 4 _yOpen Access through DSpace
_uhttp://hdl.handle.net/10883/4563
942 _2ddc
_cJA
_n0