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一个编码花粉过敏原和病程相关蛋白的桦树基因家族。

A birch gene family encoding pollen allergens and pathogenesis-related proteins.

作者信息

Swoboda I, Scheiner O, Kraft D, Breitenbach M, Heberle-Bors E, Vicente O

机构信息

Institute of Microbiology and Genetics, University of Vienna, Vienna Biocenter, Austria.

出版信息

Biochim Biophys Acta. 1994 Oct 18;1219(2):457-64. doi: 10.1016/0167-4781(94)90072-8.

DOI:10.1016/0167-4781(94)90072-8
PMID:7918643
Abstract

Bet v I, the major pollen allergen of birch (Betula verrucosa), shows high sequence homology to a family of pathogenesis-related (PR) proteins that have recently been identified in several other plant species. We have used a pollen Bet v I cDNA clone and anti-Bet v I antibodies as probes to study the expression of Bet v I genes in birch cell suspension cultures under different experimental conditions. Induction of Bet v I-related proteins was detected in immunoblots of cell extracts upon co-cultivation with microbial pathogens. Northern analysis revealed the rapid induction of Bet v I transcripts in the presence of bacteria and fungi, but not by stress treatments (heat shock, metal ions) or by chemical elicitors. RNase protection experiments showed that the pathogen-inducible RNAs did not correspond to the pollen cDNA clone but most likely to the products of transcription of other members of the Bet v I gene family, sharing high sequence homology with the pollen-specific gene within the 5'-half of the coding region. We conclude that the Bet v I gene family of pollen allergens includes a subset of defense-related genes that are transcriptionally activated in the presence of microbial pathogens.

摘要

桦树(疣枝桦)的主要花粉过敏原Bet v I与最近在其他几种植物物种中鉴定出的一类病程相关(PR)蛋白具有高度的序列同源性。我们使用花粉Bet v I cDNA克隆和抗Bet v I抗体作为探针,研究了在不同实验条件下桦树细胞悬浮培养物中Bet v I基因的表达。在与微生物病原体共培养后,在细胞提取物的免疫印迹中检测到了Bet v I相关蛋白的诱导。Northern分析显示,在存在细菌和真菌的情况下,Bet v I转录本迅速被诱导,但在应激处理(热休克、金属离子)或化学激发子处理下则未被诱导。RNase保护实验表明,病原体诱导的RNA与花粉cDNA克隆不对应,而最有可能对应于Bet v I基因家族其他成员的转录产物,在编码区5'端的一半区域内与花粉特异性基因具有高度的序列同源性。我们得出结论,花粉过敏原的Bet v I基因家族包括一组与防御相关的基因,这些基因在微生物病原体存在时会被转录激活。

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