A more precise location for the bronze mutation on LG IV

 

Weeden, N.F.                                                                                       Dept. of Plant Sci. and Plant Path.

                                                                                                  Montana State Univ.,  Bozeman,  MT USA

 

      The line E107 was obtained by  EMS mutagenesis of pea cultivar ‘Sparkle’ (2).  This line was originally isolated as a mutant that nodulated poorly, but the altered nodulation phenotype appears to be a pleiotropic effect of a modification in iron uptake that leads to high accumulation of iron in leaf cells, causing an initial chlorosis and later development of bronze colored lesions on the leaflets.  Kneen et al. (3) characterized this mutation and called the affected gene brz (bronze) after the lesion color and general tint of some of the leaflets.  The gene was located on LG IV, 0.1 + 12 cM from Was on the basis of a single cross with the two dominant genes in repulsion phase linkage (3).  Although experimental data were not presented, Ellis and Poyser (1) show Brz located approximately 10 cM distal to Was on LG IV.

      When growing populations in the artificial soil mix at Cornell, the appearance of the BRONZE phenol-type was not consistent, and mapping experiments had to be performed growing plants in vermiculite with supplemental chelated Fe2+ (3).  At  Montana State University I have been able to obtain the phenotype reliably in glasshouse-grown plants, the bronze lesions of the brz/brz homozygote being easily observed after 3 weeks growth.

      A brz, was line (C03-6c-6) was developed by crossing the original E107 line with a derivative of A583-139 (was/was).  This line was crossed with a homozygous Brz, Was line (A04-12) and the F1 grown in the field to maximize seed production.  An F2 of 221 seed was scored for recombinant phenotypes.  The joint segregation data are presented in Table 1.  Each mutant gave a segregation pattern close to the expected 3:1 ratio.  Joint segregation analysis of either Brz or Was with St gave ratios consistent with independent assortment.  However, joint segregation analysis of Brz and Was gave significant deviation from independent assortment, indicating that the two loci were separated by about 9 cM (Table 1).  These results are consistent with the two previous mapping studies and provide a more precise estimate of the linkage intensity between two loci on LG IV.

  Text Box: Table 1. Genetic analysis of segregation patterns in the cross E107(brz) x A583-139 (was) Single locus Joint segregation analysis (Brz/Was) Locus (loci) n Domin Recess Brz/Was Brz/was brz/Was brz/was c2 R + S.E. Brz 221 162 59 Was 221 156 65 St 221 158 63 Brz/Was 221 149 13 7 52 134*** 9.1 + 6.7 *** P < 0.001

 

 

 

 

1.       Ellis, T.H.N. and Poyser, S.J.  2002.  New Phytol. 153: 17-25.

2.       Kneen, B.E. and LaRue, T.A.  1988.  Plant Sci. 58: 177-182.

3.       Kneen, B.E., LaRue, T.A., Welch, R.M. and Weeden, N.F.  1990.  Plant Physiol. 93: 717-722.