Blauth S L, Yao Y, Klucinec J D, Shannon J C, Thompson D B, Guilitinan M J
The Biotechnology Institute, Pennsylvania State University, University Park, Pennsylvania 16802.
Plant Physiol. 2001 Mar;125(3):1396-405. doi: 10.1104/pp.125.3.1396.
Starch-branching enzymes (SBE) break the alpha-1,4 linkage of starch, re-attaching the chain to a glucan chain by an alpha-1,6 bond, altering starch structure. SBEs also facilitate starch accumulation by increasing the number of non-reducing ends on the growing chain. In maize (Zea mays), three isoforms of SBE have been identified. To examine the function of the SBEIIa isoform, a reverse genetics polymerase chain reaction-based screen was used to identify a mutant line segregating for a Mutator transposon within Sbe2a. To locate the insertion within the second exon of Sbe2a, the genomic sequence of Sbe2a containing the promoter and 5' end was isolated and sequenced. Plants homozygous for sbe2a::Mu have undetectable levels of Sbe2a transcripts and SBEIIa in their leaves. Characterization of leaf starch from sbe2a::Mu mutants shows reduced branching similar to yet more extreme than that seen in kernels lacking SBEIIb activity. Characterization of endosperm starch from sbe2a::Mu mutants shows branching that is indistinguishable from wild-type controls. These mutant plants have a visible phenotype resembling accelerated senescence, which was correlated with the Mutator insertion within Sbe2a. This correlation suggests a specific role for SBEIIa in leaves, which may be necessary for normal plant development.
淀粉分支酶(SBE)可断裂淀粉的α-1,4糖苷键,通过α-1,6键将链重新连接到葡聚糖链上,从而改变淀粉结构。SBE还通过增加生长链上非还原端的数量来促进淀粉积累。在玉米(Zea mays)中,已鉴定出三种SBE同工型。为了研究SBEIIa同工型的功能,采用了基于反向遗传学聚合酶链反应的筛选方法,以鉴定在Sbe2a内分离出Mutator转座子的突变系。为了定位Sbe2a第二个外显子内的插入位点,分离并测序了包含启动子和5'端的Sbe2a基因组序列。sbe2a::Mu纯合植株的叶片中检测不到Sbe2a转录本和SBEIIa。对sbe2a::Mu突变体叶片淀粉的表征显示,其分支减少,与缺乏SBEIIb活性的籽粒中观察到的情况相似但更为极端。对sbe2a::Mu突变体胚乳淀粉的表征显示,其分支与野生型对照无明显差异。这些突变植株具有类似加速衰老的可见表型,这与Sbe2a内的Mutator插入有关。这种相关性表明SBEIIa在叶片中具有特定作用,这可能是正常植物发育所必需的。