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编码表皮生长因子受体羧基末端结构域的序列差异与病毒erbB基因的疾病潜能差异相关。

Differences in sequences encoding the carboxyl-terminal domain of the epidermal growth factor receptor correlate with differences in the disease potential of viral erbB genes.

作者信息

Gamett D C, Tracy S E, Robinson H L

出版信息

Proc Natl Acad Sci U S A. 1986 Aug;83(16):6053-7. doi: 10.1073/pnas.83.16.6053.

Abstract

Eleven recently isolated erbB-transducing viruses as well as avian erythroblastosis virus (AEV)-R (ES4) and AEV-H have been characterized for the type of disease they cause, their ability to transform fibroblasts in culture, their ability to cause disease in pedigrees of chicken that differ in susceptibility to erbB-induced erythroblastosis, and the structure of their erbB genes. Differences in each of the biological parameters correlated with differences in erbB sequences encoding the C-terminal domain of the epidermal growth factor receptor (EGFR). Seven viruses were strain restricted in their ability to induce erythroblastosis and did not transform fibroblasts. These seven viruses contained v-erbB genes encoding the complete C terminus of the EGFR. AEV-R and AEV-H were not pedigree restricted in their ability to induce erythroblastosis and could transform fibroblasts. These viruses contain v-erbB genes that lack codons for the immediate C terminus of the EGFR. Three viruses caused angiosarcoma and one caused fibrosarcoma. The angiosarcoma and fibrosarcoma-inducing viruses were not strain restricted and did not cause erythroblastosis. The v-erbB genes of each of these viruses contained extensive internal deletions or 3' truncations in sequences encoding the C-terminal domain of the EGFR.

摘要

十一种最近分离出的erbB转导病毒以及禽成红细胞增多症病毒(AEV)-R(ES4)和AEV-H,已针对它们所引发的疾病类型、在培养物中转化成纤维细胞的能力、在对erbB诱导的成红细胞增多症易感性不同的鸡系中引发疾病的能力以及它们erbB基因的结构进行了表征。每个生物学参数的差异都与编码表皮生长因子受体(EGFR)C末端结构域的erbB序列差异相关。七种病毒在诱导成红细胞增多症的能力上受到毒株限制,并且不能转化成纤维细胞。这七种病毒含有编码EGFR完整C末端的v-erbB基因。AEV-R和AEV-H在诱导成红细胞增多症的能力上不受鸡系限制,并且能够转化成纤维细胞。这些病毒含有缺少EGFR紧邻C末端密码子的v-erbB基因。三种病毒引发了血管肉瘤,一种引发了纤维肉瘤。这些引发血管肉瘤和纤维肉瘤的病毒不受毒株限制,也不会导致成红细胞增多症。这些病毒中的每一种的v-erbB基因在编码EGFR C末端结构域的序列中都包含广泛的内部缺失或3'端截短。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89b3/386436/8c19e51f0c11/pnas00320-0311-a.jpg

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