Department of Biology, Texas A&M University, 77843-3258, College Station, TX, USA.
Plant Mol Biol. 1989 Mar;12(3):245-56. doi: 10.1007/BF00043202.
Electrophoretic analysis of translation products of polyadenylated RNA isolated from mid-maturation sorghum seed in the presence of [(35)S]met, [(3)H]leu, or [(3)H]val revealed two major proteins of kDa and 21 kDa. These products were not detected when [(3)H]lys was supplied as the radioactive substrate. Under similar electrophoretic conditions, kafirin (a major seed storage prolamin of sorghum), migrated as two bands of 22 kDa and 19 kDa. Sequence analysis of two cDNA clones (pSK8 and pSKR2) from sorghum seed mRNA revealed them to be highly homologous with each other and to the 22 kDa zeins from maize, suggesting that they represented kafirin cDNAs. Compared with pSKR2, pSK8 had an insertion of 24 nucleotides and a deletion of 24 nucleotides, so that the coding regions were nearly identical in length. The deduced amino acid sequence for these cDNA clones reveals that kafirin, like zein, is rich in glutamine and nonpolar amino acids, but contains no lysine. Both kafirin and zein have a 21 amino acid signal peptide exhibiting 80% homology and eight copies of a repetitive amino acid block in the C-terminal domain with the consensus: infI (supP) LL finP (supA) LN infQ (supP) LALANPAAYLQQQQ.The kafirin cDNAs were used as probes to screen a sorghum genomic library; one genomic clone (λGK.1) was sequenced and found to be very similar (97.8%) to the pSK8 cDNA clone. Clone λGK.1 contains features typical for a functional gene in that the intronless open reading frame encoding 268 amino acids is flanked at the 5' end by sequences corresponding to the CAAT and TATA promoter boxes (positioned at about -60 and -30 bp, respectively, from the transcriptional initiation site), and at the 3' end by a consensus polyadenylation signal. In common with zein genomic clones, kafirin clones contain a 15 basepair consensus sequence centered at postion -320 relative to the transcriptional initiation site. Under similar hybridization conditions, genomic reconstruction analysis using an oligonucleotide probe indicated the presence of less than 20 copies of kafirin per haploid sorghum genome compared with approximatley 140 copies of zein per haploid maize genome.
从中期成熟高粱种子中分离的多聚腺苷酸化 RNA 的翻译产物经 [(35)S]Met、[(3)H]Leu 或 [(3)H]Val 进行电泳分析显示出 21 kDa 和 21 kDa 的两种主要蛋白质。当 [(3)H]Lys 作为放射性底物供应时,未检测到这些产物。在类似的电泳条件下,高粱种子贮藏蛋白醇溶蛋白(kafirin)迁移为 22 kDa 和 19 kDa 的两个条带。高粱种子 mRNA 的两个 cDNA 克隆(pSK8 和 pSKR2)的序列分析表明它们彼此高度同源,与玉米的 22 kDa 玉米醇溶蛋白相似,表明它们代表 kafirin cDNA。与 pSKR2 相比,pSK8 有 24 个核苷酸的插入和 24 个核苷酸的缺失,因此编码区的长度几乎相同。这些 cDNA 克隆的推导氨基酸序列表明,kafirin 与醇溶蛋白一样富含谷氨酰胺和非极性氨基酸,但不含赖氨酸。kafirin 和醇溶蛋白都有一个 21 个氨基酸的信号肽,其 80%同源,在 C 末端结构域中有 8 个重复的氨基酸块,其共有序列为:infI(supP)LL finP(supA)LN infQ(supP)LALANPAAYLQQQQ。kafirin cDNA 用作探针筛选高粱基因组文库;一个基因组克隆(λGK.1)被测序并发现与 pSK8 cDNA 克隆非常相似(97.8%)。克隆 λGK.1 包含一个无内含子的开放阅读框,编码 268 个氨基酸,其 5' 端侧翼序列与 CAAT 和 TATA 启动子盒相对应(分别位于转录起始位点的约-60 和-30 bp 处),3' 端侧翼序列与聚腺苷酸化信号一致。与醇溶蛋白基因克隆一样,kafirin 克隆在转录起始位点相对位置-320 处包含一个 15 个碱基对的共有序列。在类似的杂交条件下,使用寡核苷酸探针进行基因组重建分析表明,高粱单倍体基因组中 kafirin 的拷贝数少于 20 个,而玉米单倍体基因组中醇溶蛋白的拷贝数约为 140 个。