Mitchell-Olds T, Pedersen D
Max-Planck-Institut für Chemishe Okologie, 07745 Jena, Germany.
Genetics. 1998 Jun;149(2):739-47. doi: 10.1093/genetics/149.2.739.
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.
为了找到控制数量变异的基因,我们需要模型系统,在该系统中,有关生理学、发育和基因调控的功能信息能够指导进化推断。我们绘制了影响拟南芥初生和次生代谢中酶活性数量水平的数量性状基因座(QTL)图谱。所有10种酶都表现出高度显著的数量遗传变异。在5种糖酵解酶(PGI、PGM、GPD、FBP和G6P)的活性水平之间发现了强正遗传相关性,这表明具有密切相关代谢功能的酶是共同调控的。发现了影响大多数酶活性的显著QTL。一些酶活性QTL与已知的酶编码基因座(如己糖激酶、PGI和PGM)定位非常接近。一个己糖激酶QTL归因于AtHXK1基因座或紧密连锁的调控基因座上的顺式作用调控变异,而非多肽序列差异。我们还在第四条染色体上发现了一个QTL,它可能是GPD、PGI和G6P活性的联合调节因子。此外,一个影响PGM活性的QTL定位在PGM编码基因座的700 kb范围内。预计这个QTL会使淀粉生物合成改变3.4%,这与理论模型相符,表明QTL反映了突变等位基因的多效性效应。