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与生长素诱导侧根形成过程中积累的mRNA相对应的cDNA克隆的分离与鉴定。

Isolation and characterization of cDNA clones corresponding with mRNAs that accumulate during auxin-induced lateral root formation.

作者信息

Neuteboom L W, Ng J M, Kuyper M, Clijdesdale O R, Hooykaas P J, van der Zaal B J

机构信息

Institute of Molecular Plant Sciences, Leiden University, Wassenaarseweg, The Netherlands.

出版信息

Plant Mol Biol. 1999 Jan;39(2):273-87. doi: 10.1023/a:1006104205959.

Abstract

Lateral root formation in root cultures of Arabidopsis thaliana can be initiated by exogenous addition of auxin. In order to find cDNA clones of which the corresponding mRNAs accumulate during this process, a cDNA library was constructed from root cultures treated with the active auxin 1-naphthaleneacetic acid (1-NAA). Differential screening of this library with cDNA probes derived from mRNA populations isolated from root cultures treated with 1-NAA and the inactive analogue 2-naphthaleneacetic acid (2-NAA) led to the isolation of four cDNA clones, designated AIR1, AIR3, AIR9 and AIR12. Accumulation of the mRNAs starts between 4 and 8 h and continues till at least 24 h after addition of an active auxin. Sequence analysis revealed that AIR1 encodes a protein that is related to a large family of proteins that consist of a proline-rich or glycine-rich N-terminus and a hydrophobic, possibly membrane spanning C-terminus. The putative function of these proteins is coupling of the cell wall to the plasma membrane. Surprisingly, AIR1 lacks the proline-rich or glycine-rich N-terminus which is thought to be important for interaction with the cell wall. AIR3 encodes a subtilisin-like serine protease which is believed to be active outside the plant cell. Although AIR9 and AIR12 do not show any significant homology to sequences in the database, they are also predicted to function outside the cell. Our screening thus indicates that a variety of genes encoding extracellular proteins are activated during auxin-induced lateral root formation.

摘要

拟南芥根培养物中的侧根形成可通过外源添加生长素来启动。为了找到在这个过程中相应mRNA积累的cDNA克隆,用活性生长素1-萘乙酸(1-NAA)处理的根培养物构建了一个cDNA文库。用从用1-NAA和无活性类似物2-萘乙酸(2-NAA)处理的根培养物中分离的mRNA群体衍生的cDNA探针,对该文库进行差异筛选,从而分离出四个cDNA克隆,命名为AIR1、AIR3、AIR9和AIR12。添加活性生长素后,mRNA的积累在4至8小时之间开始,并至少持续到24小时。序列分析表明,AIR1编码一种蛋白质,该蛋白质与一大类蛋白质相关,这类蛋白质由富含脯氨酸或富含甘氨酸的N端和疏水的、可能跨膜的C端组成。这些蛋白质的假定功能是将细胞壁与质膜连接起来。令人惊讶的是,AIR1缺乏被认为对与细胞壁相互作用很重要的富含脯氨酸或富含甘氨酸的N端。AIR3编码一种枯草杆菌蛋白酶样丝氨酸蛋白酶,据信该蛋白酶在植物细胞外具有活性。尽管AIR9和AIR12与数据库中的序列没有任何显著同源性,但它们也被预测在细胞外发挥作用。因此,我们的筛选表明,在生长素诱导的侧根形成过程中,多种编码细胞外蛋白的基因被激活。

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