Molecular cloning and characterization of the amylose-extender gene encoding starch branching enzyme IIB in maize

被引:74
作者
Kim, KN
Fisher, DK
Gao, M
Guiltinan, MJ [1 ]
机构
[1] Penn State Univ, Inst Biotechnol, Intercoll Grad Program Plant Physiol, University Pk, PA 16802 USA
[2] Penn State Univ, Inst Biotechnol, Intercoll Grad Program Genet, University Pk, PA 16802 USA
[3] Penn State Univ, Dept Hort, University Pk, PA 16802 USA
关键词
amylose-extender; Ae; genomic organization; promoter analysis; Zea mays L; starch-branching enzyme;
D O I
10.1023/A:1006057609995
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The amylose-extender (Ae) gene encoding starch-branching enzyme IIb (SBEIIb) in maize is predominantly expressed in endosperm and embryos during kernel development. A maize genomic DNA fragment (-2964 to +20485) containing the Ae gene was isolated and sequenced. The maize Ae mRNA is derived from 22 exons distributed over 16914 bp. Twenty-one introns, differing in length from 76 bp to 4020 bp, all have conserved junction sequences (GT..AG). Sequence analysis of the 5'- and 3'-flanking regions revealed a consensus TATA-box sequence located 28 bp upstream of the transcription initiation site as determined by primer extension analysis, and a putative polyadenylation signal observed 29 bp upstream of the polyadenylation site based on cDNA sequence. Genomic Southern blot analysis suggests that a single Ae gene is present in the maize genome. Promoter activity was confirmed by testing a transcriptional fusion of the Ae 5'-flanking region between -2964 and +100 to a luciferase reporter gene in a transient expression assay using maize endosperm suspension cultured cells. 5' deletion analysis revealed that the 111 bp region from -160 to -50 is essential for high-level promoter activity.
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页码:945 / 956
页数:12
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