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巴西橡胶树橡胶延长因子cDNA的克隆与测序

Cloning and Sequencing of the cDNA Encoding the Rubber Elongation Factor of Hevea brasiliensis.

作者信息

Goyvaerts E, Dennis M, Light D, Chua N H

机构信息

Institute of Molecular and Cell Biology, National University of Singapore, Singapore 0511.

出版信息

Plant Physiol. 1991 Sep;97(1):317-21. doi: 10.1104/pp.97.1.317.

Abstract

In Hevea brasiliensis, the rubber particle in the laticiferous vessel is the site of rubber (cis-1-4-polyisoprene) biosynthesis. A 14 kilodalton protein, rubber elongation factor (REF), is associated with the rubber particle in a ratio of one REF to one rubber molecule (Dennis M, Henzel W, Bell J, Kohr W, Light D [1989] J Biol Chem 264: 18618-18628; Dennis M, Light D [1989] J Biol Chem 264: 18608-18617). To obtain more information concerning the function of REF and its synthesis and assembly in the rubber particle, we isolated cDNA clones encoding REF. We used antibodies to REF to screen a Hevea leaf gammagt11 cDNA expression library and obtained several positive clones. Sequence analysis of the REF cDNA clones showed that the REF mRNA contains 121 nucleotides of 5'-nontranslated sequences and a 205 nucleotide 3'-nontranslated region. The open reading frame encodes the entire 14 kilodalton REF protein without any extra amino acids (Dennis M, Henzel W, Bell J, Kohr W, Light D [1989] J Biol Chem 264: 18618-18628). The REF cDNA was subcloned in pGEM-3Z/-4Z and expressed in vitro. The translation product is a 14 kilodalton protein that can be immunoprecipitated with antibodies to REF. Addition of microsomal membranes to the in vitro translation product did not alter the mobility of the REF protein. This, and the sequence data, indicate that REF is not made as a preprotein. Our results suggest that REF is synthesized on free polysomes in the laticifer cytoplasm and that assembly of the rubber particles is likely to occur in the cytosol.

摘要

在巴西橡胶树中,乳汁管中的橡胶粒子是橡胶(顺式-1,4-聚异戊二烯)生物合成的场所。一种14千道尔顿的蛋白质,橡胶延长因子(REF),以一个REF对应一个橡胶分子的比例与橡胶粒子结合(丹尼斯·M、亨泽尔·W、贝尔·J、科尔·W、莱特·D [1989]《生物化学杂志》264: 18618 - 18628;丹尼斯·M、莱特·D [1989]《生物化学杂志》264: 18608 - 18617)。为了获得更多关于REF的功能及其在橡胶粒子中的合成与组装的信息,我们分离了编码REF的cDNA克隆。我们用针对REF的抗体筛选巴西橡胶树叶γgt11 cDNA表达文库,并获得了几个阳性克隆。对REF cDNA克隆的序列分析表明,REF mRNA包含121个核苷酸的5' - 非翻译序列和一个205个核苷酸的3' - 非翻译区。开放阅读框编码整个14千道尔顿的REF蛋白,没有任何额外的氨基酸(丹尼斯·M、亨泽尔·W、贝尔·J、科尔·W、莱特·D [1989]《生物化学杂志》264: 18618 - 18628)。REF cDNA被亚克隆到pGEM - 3Z / - 4Z中并在体外表达。翻译产物是一种14千道尔顿的蛋白质,它可以被针对REF的抗体免疫沉淀。将微粒体膜添加到体外翻译产物中并没有改变REF蛋白的迁移率。这一点以及序列数据表明,REF不是以前体蛋白的形式产生的。我们的结果表明,REF是在乳汁细胞胞质中的游离多核糖体上合成的,并且橡胶粒子的组装可能发生在细胞质溶胶中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b22/1081000/28e619b233fa/plntphys00696-0329-a.jpg

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