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. 2006 Jan;18(1):212–224. doi: 10.1105/tpc.105.037077

Figure 3.

Figure 3.

Map-Based Identification of the vte5-1 Mutation.

(A) Low-resolution mapping. Four hundred F3 plants were genotyped to show linkage to the genetic markers MOK16_64764 and MAC12_30751 on chromosome V. cM, centimorgan.

(B) Narrowing the interval between two core markers. Additional markers were assayed to identify a 700-kb region containing the mutation.

(C) High-resolution mapping. An additional 2000 F3 plants were scored using single nucleotide polymorphism markers within the 700-kb region. Markers T32M21_26901 and T32M21_66646 were found to be the closest flanking markers based on the available recombinants, narrowing the interval to 37 kb.

(D) The entire 37-kb region containing seven open reading frames (ORFs) was sequenced from the lt1 mutant.

(E) A single G→A point mutation was detected in exon 5 of T32M21_90. It is predicted to convert a Trp codon to an opal nonsense codon.