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Molecular structure of three mutations at the maize sugary1 locus and their allele-specific phenotypic effects

机译:玉米sugary1基因座上三个突变的分子结构及其等位基因特异性表型效应

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Starch production in all plants examined is altered by mutations of isoamylase-type starch-debranching enzymes (DBE), although how these proteins affect glucan, polymer assembly is not understood. Various allelic mutations in the maize (Zen mays) gene sugary1 (su1), which codes for an isoamylase-type DBE, condition distinct kernel phenotypes. This study characterized the recessive mutations su1-Ref, su1-R4582::Mu1, and su1-st, regarding their molecular basis, chemical phenotypes, and effects on starch metabolizing enzymes. The su1-R4582::Mu1 mutation is a null allele that abolishes transcript accumulation. The Su1-st mutation results from insertion of a novel transposon-like sequence, designated Toad, ahich causes alternative without affecting the Su1 mRNA level. The su1-R4582::Mu1 mutation is a null allele that abolishes transcript accumulation. The su1-st mutation results from insertion of a novel transposon-like sequence, designated Toad which causes alternative pre-mRNA splicing. Three su1-st mutant transcripts are produced, one that is nonfunctional and two that code for modified SU1 polypetides. The su2-st mutation is dominant to the null allele su1-R4582::Mu1 but recessive to su1-Ref, suggestive of complex effects involving quaternary structure of the SU1 enzyme. All three su1- alleles severely reduce or eliminate isoamylase-type DBE activity, although su1-st kernels accumulate less phytoglycogen and Suc than su1-Ref or su1-R4587::Mu1 mutants. The chain length distribution of residual amylopectin is significantly altered by su1-Ref and su1-R4582::Mu1 whereas su1-st has modest effects. These results, together with sill allele-specific effects on other starch-metabolizing enzymes detected in zymograms, suggest that total DBE catalytic activity is the not the sole determinant of Su1 function and that specific interactions between SU1 and other components of the starch biosynthetic system are required. [References: 44]
机译:异淀粉酶型淀粉脱支酶(DBE)的突变改变了所有受检植物的淀粉产量,尽管这些蛋白质如何影响葡聚糖,但尚不清楚聚合物组装。玉米(Zen mays)基因sugary1(su1)中的各种等位基因突变编码异淀粉酶型DBE,可调节不同的籽粒表型。这项研究对隐性突变su1-Ref,su1-R4582 :: Mu1和su1-st的分子基础,化学表型以及对淀粉代谢酶的影响进行了表征。 su1-R4582 :: Mu1突变是无效的等位基因,可消除转录本的积累。 Su1-st突变是由插入名为Toad的新型转座子样序列导致的,这导致了另一种选择而不影响Su1 mRNA的水平。 su1-R4582 :: Mu1突变是无效的等位基因,可消除转录本的积累。 su1-st突变是由插入新的转座子样序列(称为Toad)导致的,该序列导致了替代的前mRNA剪接。产生了三个su1-st突变体转录本,一个是无功能的,两个是编码修饰的SU1多肽的。 su2-st突变主要用于无效等位基因su1-R4582 :: Mu1,但对su1-Ref则是隐性的,提示涉及SU1酶四级结构的复杂效应。尽管与su1-Ref或su1-R4587 :: Mu1突变体相比,su1-st谷粒积累的植物糖原和Suc更少,但所有三个su1-等位基因均会严重降低或消除异淀粉酶型DBE活性。 su1-Ref和su1-R4582 :: Mu1显着改变了残留支链淀粉的链长分布,而su1-st的影响不大。这些结果,以及在酶谱图中检测到的对其他淀粉代谢酶的基尔等位基因特异性影响,表明总DBE催化活性不是Su1功能的唯一决定因素,SU1与淀粉生物合成系统其他组分之间的特异性相互作用是需要。 [参考:44]

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