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. 1998 Jun;149(2):739-47.
doi: 10.1093/genetics/149.2.739.

The molecular basis of quantitative genetic variation in central and secondary metabolism in Arabidopsis

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The molecular basis of quantitative genetic variation in central and secondary metabolism in Arabidopsis

T Mitchell-Olds et al. Genetics. 1998 Jun.

Abstract

To find the genes controlling quantitative variation, we need model systems where functional information on physiology, development, and gene regulation can guide evolutionary inferences. We mapped quantitative trait loci (QTLs) influencing quantitative levels of enzyme activity in primary and secondary metabolism in Arabidopsis. All 10 enzymes showed highly significant quantitative genetic variation. Strong positive genetic correlations were found among activity levels of 5 glycolytic enzymes, PGI, PGM, GPD, FBP, and G6P, suggesting that enzymes with closely related metabolic functions are coregulated. Significant QTLs were found influencing activity of most enzymes. Some enzyme activity QTLs mapped very close to known enzyme-encoding loci (e.g., hexokinase, PGI, and PGM). A hexokinase QTL is attributable to cis-acting regulatory variation at the AtHXK1 locus or a closely linked regulatory locus, rather than polypeptide sequence differences. We also found a QTL on chromosome IV that may be a joint regulator of GPD, PGI, and G6P activity. In addition, a QTL affecting PGM activity maps within 700 kb of the PGM-encoding locus. This QTL is predicted to alter starch biosynthesis by 3.4%, corresponding with theoretical models, suggesting that QTLs reflect pleiotropic effects of mutant alleles.

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    1. Genetics. 1996 Apr;142(4):1305-19 - PubMed
    1. Genetics. 1992 Oct;132(2):603-18 - PubMed
    1. Genetics. 1991 Jan;127(1):181-97 - PubMed
    1. Genetics. 1995 Jan;139(1):337-48 - PubMed
    1. Genetics. 1992 Sep;132(1):163-78 - PubMed

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