Perlick A M, Pühler A
Lehrstuhl für Genetik, Fakultät für Biologie, Universität Bielefeld, Germany.
Plant Mol Biol. 1993 Sep;22(6):957-70. doi: 10.1007/BF00028969.
More than 600 potentially nodule-specific clones have been detected by differential hybridization of a broadbean cDNA library constructed from root nodule poly(A)+ RNA. These isolated cDNAs belong to at least 28 different clone groups containing cross-hybridizing sequences. The number of clones within a clone group varies from about 200 to only one single clone. Northern hybridization experiments revealed nodule-specific transcripts for 14 clone groups and markedly nodule-enhanced transcripts for another 7 clone groups. Sequence homologies indicate that three transcript sequences code for different leghemoglobins. Two other transcripts encode a nodule-specific sucrose synthase and a nodule-enhanced asparagine synthetase, respectively. Four deduced gene products are proline-rich, two of them being the homologues of PsENOD2 and PsENOD12. The third proline-rich protein (PRP) is composed of similar amino acid repeats as the nodule-specific PsENOD12 but is expressed in nodules and roots in comparable amounts. The fourth PRP is a nodule-enhanced extensin-type protein built up by Ser-Pro4 repeats. Two further nodule-specific transcripts encode gene products showing some similarity to structural glycine-rich proteins. Additionally, transcripts could be identified for broadbean homologues of the nodulins MsNOD25, PsENOD3 and PsENOD5 and transcripts specifying a nodule-enhanced lipoxygenase and a translation elongation factor EF-1 alpha, which is expressed in all broadbean tissues tested.
通过对从根瘤多聚腺苷酸加尾RNA构建的蚕豆cDNA文库进行差异杂交,已检测到600多个可能具有结节特异性的克隆。这些分离出的cDNA属于至少28个不同的克隆组,其中包含交叉杂交序列。一个克隆组内的克隆数量从约200个到仅一个单个克隆不等。Northern杂交实验揭示了14个克隆组的结节特异性转录本以及另外7个克隆组的明显结节增强转录本。序列同源性表明,三个转录本序列编码不同的豆血红蛋白。另外两个转录本分别编码一种结节特异性蔗糖合酶和一种结节增强型天冬酰胺合成酶。四个推导的基因产物富含脯氨酸,其中两个是PsENOD2和PsENOD12的同源物。第三种富含脯氨酸的蛋白质(PRP)由与结节特异性PsENOD12相似的氨基酸重复序列组成,但在结节和根中的表达量相当。第四个PRP是一种由Ser-Pro4重复序列构成的结节增强型伸展蛋白。另外两个结节特异性转录本编码的基因产物与富含甘氨酸的结构蛋白有一定相似性。此外,还可鉴定出结节素MsNOD25、PsENOD3和PsENOD5的蚕豆同源物的转录本,以及一个指定结节增强型脂氧合酶和一个在所有测试的蚕豆组织中均有表达的翻译延伸因子EF-1α的转录本。