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赤霉素和脱落酸对大麦糊粉层中α-淀粉酶 mRNA 水平的影响研究,使用α-淀粉酶 cDNA 克隆。

The effects of gibberellic acid and abscisic acid on α-amylase mRNA levels in barley aleurone layers studies using an α-amylase cDNA clone.

机构信息

CSIRO Division of Protein Chemistry, 343 Royal Parade, 3052, Parkville, Victoria, Australia.

出版信息

Plant Mol Biol. 1984 Nov;3(6):407-18. doi: 10.1007/BF00033389.

Abstract

Two cDNA clones were characterized which correspond to different RNA species whose level is increased by gibberellic acid (GA3) in barley (Hordeum vulgare L.) aleurone layers. On the criteria of amino terminal sequencing, amino acid composition and DNA sequencing it is likely that one of these clones (pHV19) corresponds to the mRNA for α-amylase (1,4-α-D-glucan glucanohydrolase, EC 3.2.1.1.), in particular for the B family of α-amylase isozymes (Jacobsen JV, Higgins TJV: Plant Physiol 70:1647-1653, 1982). Sequence analysis of PHV19 revealed a probable 23 amino acid signal peptide. Southern hybridization of this clone to barley DNA digested with restriction endonucleases indicated approximately eight gene-equivalents per haploid genome.The identity of the other clone (pHV14) is unknown, but from hybridization studies and sequence analysis it is apparently unrelated to the α-amylase clone.Both clones hybridize to RNAs that are similar in size (∼1500b), but which accumulate to different extents following GA3 treatment: α-amylase mRNA increases approximately 50-fold in abundance over control levels, whereas the RNA hybridizing to pHV14 increases approximately 10-fold. In the presence of abscisic acid (ABA) the response to GA3 is largely, but not entirely, abolished. These results suggest that GA3 and ABA regulate synthesis of α-amylase in barley aleurone layers primarily through the accumulation of α-amylase mRNA.

摘要

两个 cDNA 克隆被鉴定,它们对应于不同的 RNA 种类,其水平在大麦糊粉层中被赤霉素(GA3)增加。根据氨基末端测序、氨基酸组成和 DNA 测序的标准,这些克隆之一(pHV19)很可能对应于α-淀粉酶(1,4-α-D-葡聚糖葡聚糖水解酶,EC 3.2.1.1.)的 mRNA,特别是 B 家族的α-淀粉酶同工酶(Jacobsen JV,Higgins TJV:植物生理学 70:1647-1653,1982)。对 pHV19 的序列分析揭示了一个可能的 23 个氨基酸信号肽。该克隆对用限制内切酶消化的大麦 DNA 的 Southern 杂交表明,每个单倍体基因组约有 8 个基因当量。另一个克隆(pHV14)的身份未知,但从杂交研究和序列分析来看,它显然与α-淀粉酶克隆无关。两个克隆都与大小相似(约 1500b)的 RNA 杂交,但在 GA3 处理后积累程度不同:α-淀粉酶 mRNA 的丰度增加了约 50 倍,而与 pHV14 杂交的 RNA 增加了约 10 倍。在脱落酸(ABA)存在的情况下,GA3 的反应在很大程度上但不完全被废除。这些结果表明,GA3 和 ABA 主要通过积累α-淀粉酶 mRNA 来调节大麦糊粉层中α-淀粉酶的合成。

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