Li Z, Wurtzel E T
Department of Biological Sciences, Lehman College and The Graduate School and University Center, City University of New York, Bronx 10468, USA.
Plant Mol Biol. 1998 Jul;37(5):749-61. doi: 10.1023/a:1006012530241.
We describe the isolation and characterization of maize cDNAs that are transcribed from a small gene family and encode a novel group of receptor-like kinases (RLKs). The distinctive extracellular domain of these novel RLKs includes a unique number and arrangement of leucine-rich repeats (LRRs), a proline-rich region (PRR), a putative protein degradation target sequence (PEST), and a serine-rich region (SRR). The intracellular domain contains a putative serine/threonine protein kinase. To distinguish them from other reported RLKs, these novel RLKs were termed leucine-rich repeat transmembrane protein kinases (LTKs). Based on analysis of available deduced protein sequences, LTK1 and LTK2 were predicted to be 92.1% identical, while LTK2 and LTK3 were predicted to be 97.5% identical. Though the three LTK proteins showed high homology, the region that most distinguished LTK1 from LTK2 and LTK3 was found in the extracellular domain, in the SRR. To differentiate between expression of the individual ltk genes, we used the reverse transcriptase polymerase chain reaction (RT-PCR) in combination with restriction enzyme analysis. While ltk1 transcripts were constantly present in all tissues tested, ltk2 and ltk3 transcripts were only detected in the endosperm. Furthermore, transcript levels for both ltk1 and ltk2 showed modulation during endosperm development, peaking at 20 days after pollination. These results suggest that members of the ltk gene family mediate signals associated with seed development and maturation.
我们描述了从一个小基因家族转录而来、编码一组新型类受体激酶(RLK)的玉米cDNA的分离和特性分析。这些新型RLK独特的细胞外结构域包括富含亮氨酸重复序列(LRR)的独特数量和排列、富含脯氨酸区域(PRR)、一个假定的蛋白质降解靶序列(PEST)以及富含丝氨酸区域(SRR)。细胞内结构域含有一个假定的丝氨酸/苏氨酸蛋白激酶。为了将它们与其他已报道的RLK区分开来,这些新型RLK被命名为富含亮氨酸重复跨膜蛋白激酶(LTK)。基于对现有推导蛋白质序列的分析,预测LTK1和LTK2的同一性为92.1%,而LTK2和LTK3的同一性为97.5%。尽管这三种LTK蛋白显示出高度同源性,但在细胞外结构域的SRR中发现了最能区分LTK1与LTK2和LTK3的区域。为了区分各个ltk基因的表达,我们将逆转录聚合酶链反应(RT-PCR)与限制性酶切分析相结合。虽然ltk1转录本在所有测试组织中均持续存在,但ltk2和ltk3转录本仅在胚乳中检测到。此外,ltk1和ltk2的转录水平在胚乳发育过程中均表现出调节作用,在授粉后20天达到峰值。这些结果表明ltk基因家族的成员介导与种子发育和成熟相关的信号。