Rp. Koester et al., IDENTIFICATION OF QUANTITATIVE TRAIT LOCI CONTROLLING DAYS TO FLOWERING AND PLANT HEIGHT IN 2 NEAR-ISOGENIC LINES OF MAIZE, Crop science, 33(6), 1993, pp. 1209-1216
The number of days from planting to flowering is a trait of interest t
o maize (Zea mays L.) breeders for its importance in selecting appropr
iate hybrid parents, and for its role in the utilization of unadapted
germplasm. Using molecular marker technology, we were able to identify
quantitative trait loci (QTLs) controlling days to flowering and two
correlated traits, plant height and total leaf number, in two near iso
genic lines (NILs). NC264 and B73G are shorter, earlier versions of SC
76 and B73 respectively, developed by introgressing Gaspe Flint and se
lecting for early flowering through repeated backcrosses. The NILs wer
e screened for introgressed chromosomal regions with restriction fragm
ent length polymorphisms (RFLPs). Seven introgressed regions were iden
tified in NC264 and two in B73G, with a specific chromosome 8 region m
aintained in both NILs. The introgressed regions were tested for their
effect on flowering date and plant height in segregating F-2 populati
ons and F-3 families developed from crosses between the original inbre
d and the NIL. The NC264 x SC76 F-2 population was tested in both long
and short-day photoperiod environments. The RFLP analysis of the F-2
individuals and F-3 families identified major QTLs for days to floweri
ng and plant height on chromosomes 1, 8, and 10. Major QTLs for total
leaf number were found on chromosomes 1 and 8. Single-factor analysis
of variance techniques were employed for all pairwise marker trait ass
ociations. Additive gene action predominated at all loci. The most sig
nificant effects were constant across environments, generations, and p
opulations except for the region on chromosome 8, which was not signif
icant in the short-day photoperiod environment. Thus, the maturity QTL
on chromosome 8 may represent a photoperiod response element. Selecti
ve determination of genotype using only the top and bottom 10% of the
phenotypic extremes to identify QTLs was as effective as analysis of t
he entire population for detecting the most significant marker trait a
ssociations.