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植物抗体基因工程:Ⅳ.马铃薯Y病毒小鼠中和抗体重链基因的序列分析及其植物表达 被引量:1

Antibody Genetic Engineering in Plant: N. Sequencing of a Heavy Chain Gene against Potato Virus Y and Construction of Its Plant Expression Vector
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摘要 序列分析表明,马铃薯Y病毒小鼠中和抗体重链基因(G9)全长为1505个核苷酸碱基(不包括Poly(A)尾巴),其中包括5'端非编码区16个核苷酸碱基、编码重链信号肽的57个核苷酸碱基、编码成熟蛋白的1329个核苷酸碱基和3'端非编码区的103个核苷酸碱基。与已知的小鼠抗体Mopc21的重链基因(γ1)相比,核苷酸的序列同源性为94.4%,由核苷酸序列所推导出的氨基酸序列同源性为92.6%,其中可变区内(VH)的氨基酸序列同源性达74.5%,这表明二者起源于同一种系基因。将完整的抗体重链基因正向插入植物表达载体pBⅠ121中的原GUS基因位置上,置于花椰莱花叶病毒35S启动子控制之下,获得了能够在植物细胞内表达马铃薯Y病毒中和抗体重链基因的植物表达载体pYH。 Sequence analysis showed that the immunoglobulin messenger RNA corresponding to G9 is 1505 nucleotides in length excluding the poly (A ) region, among which 16 bases cede for the 51 non-coding region, 57 for the leader sequence of the protein, 1329 for the mature protein and 103 for the 3' noncoding region. Comparison of G9 with the heavy chain gene of Mopc21 showed that they share a 94. 4 % identity in nucleotide sequence and 92. 6% identity in amino acid sequence. The heavy chain encoded by G9 was considered to be specific to PVY since only one type of heavy chain was expressed in the hybridoma. A binary vector, pYH, containing the light chain gene has been constructed for its expression in higher plants by introduction of the gene coding sequence into pBI121 instead of GUS gene.
出处 《高技术通讯》 CAS CSCD 1996年第4期8-11,共4页 Chinese High Technology Letters
基金 国家自然科学基金 世界青年科学基金
关键词 马铃薯Y病毒 单克隆抗体 植物表达载体 Potato virus Y Immunoglobulin Heavy chain (γ1) Sequence analysis Plant expression vector
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