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在拟南芥种子成熟过程中,两种不同的类Em基因得以表达。

Two different Em-like genes are expressed in Arabidopsis thaliana seeds during maturation.

作者信息

Gaubier P, Raynal M, Hull G, Huestis G M, Grellet F, Arenas C, Pagès M, Delseny M

机构信息

Laboratoire de Physiologie et Biologie Moléculaire Végétales, URA 565 du CNRS, Université de Perpignan, France.

出版信息

Mol Gen Genet. 1993 Apr;238(3):409-18. doi: 10.1007/BF00292000.

Abstract

Using a radish cDNA probe, we have isolated and characterized two genomic clones from Arabidopsis thaliana (GEA1 and GEA6) encoding two different proteins that are homologous to the "Early methionine-labelled" (Em) protein of wheat. GEA1 differs from GEA6 and Em clones of wheat in that a sequence coding for 20 amino acid residues is tandemly repeated 4 times. These two genomic clones correspond to two genes named AtEm1 and AtEm6. Sequencing of several cDNA clones showed that both genes are expressed. The transcription start site was determined for both genes by RNase mapping. The site of polyadenylation is variable and there is no obvious consensus sequence for polyadenylation at the 3' ends of the genes. mRNA corresponding to GEA6 is present only in nearly dry and dry seeds, whereas the corresponding to GEA1 appears in immature seeds and is maximum in dry seeds. No expression of either gene could be detected in leaf, stem, or floral buds. Expression of both genes could be detected in immature seeds when the siliques were incubated with abscisic acid (ABA), demonstrating that both genes are ABA responsive. However, examination of the 5' upstream region does not reveal any extensive homology, suggesting that regulation of the two genes differs. In situ hybridization with a GEA1 probe demonstrated that the expression of this gene is essentially located in the provascular tissues of the cotyledons and axis of the dry seed as well as in the epiderm and outer layers of the cortex in the embryo axis.

摘要

利用萝卜cDNA探针,我们从拟南芥中分离并鉴定了两个基因组克隆(GEA1和GEA6),它们编码两种不同的蛋白质,与小麦的“早期甲硫氨酸标记”(Em)蛋白同源。GEA1与小麦的GEA6和Em克隆不同,在于一个编码20个氨基酸残基的序列串联重复了4次。这两个基因组克隆对应于两个名为AtEm1和AtEm6的基因。对几个cDNA克隆的测序表明这两个基因都有表达。通过RNA酶图谱确定了这两个基因的转录起始位点。聚腺苷酸化位点是可变的,并且在基因的3'端没有明显的聚腺苷酸化共有序列。对应于GEA6的mRNA仅存在于接近干燥和干燥的种子中,而对应于GEA1的mRNA出现在未成熟种子中,在干燥种子中含量最高。在叶、茎或花芽中未检测到任何一个基因的表达。当角果用脱落酸(ABA)处理时,在未成熟种子中可检测到这两个基因的表达,表明这两个基因对ABA有反应。然而,对5'上游区域的检查未发现任何广泛的同源性,这表明这两个基因的调控方式不同。用GEA1探针进行原位杂交表明,该基因的表达主要位于干燥种子子叶和胚轴的原维管组织以及胚轴皮层的表皮和外层。

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