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Published online 24 February 2006
Published in Crop Sci 46:834-839 (2006)
© 2006 Crop Science Society of America
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Fine Mapping of a Seed Protein QTL on Soybean Linkage Group I and Its Correlated Effects on Agronomic Traits

D. M. Nicholsa, K. D. Gloverb, S. R. Carlsonc, J. E. Spechtd and B. W. Diersa,*

a Dep. of Crop Sciences, University of Illinois, Urbana, IL 61801
b Plant Science Dep., South Dakota State University, Brookings, SD 57007
c Chromatin, Inc., 60 Hazelwood Dr., Champaign, IL 61820
d Dep. of Agronomy and Horticulture, University of Nebraska, Lincoln, NE 68583


Figure 1
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  		Fig. 1. Depiction of intervals on linkage group (LG) I that were (1) segregating (shaded with vertical markings), (2) contained a crossover (shaded with cross markings), or (3) were fixed for A81–356022 (no shading), the recurrent parent, for each of the Set 1 (A) and Set 2 (B) populations. Marker order (left) and map distances in centimorgans (right) are based on a linkage analysis across the three Set 1 populations. AAC32, ACG9a, and ACG9b are amplified fragment length polymorphism markers, and all others are simple sequence repeat markers. Shown below the linkage maps are the mean differences between lines in each population that were homozygous for G. soja or G. max alleles at Satt239 or Satt496, which were the genetic markers with the largest or nearly the largest R2 value in each population. Positive allele values are used when the G. soja alleles had a positive numerical effect on the trait. Not significant and significant at 0.05, 0.01, and 0.001 probability levels are shown by NS, *, **, and ***, respectively.

 




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