Brockus C W, Jackwood M W, Harmon B G
Department of Veterinary Pathology, College of Veterinary Medicine, University of Georgia, Athens 30602, USA.
Anim Genet. 1998 Aug;29(4):283-9. doi: 10.1046/j.1365-2052.1998.00338.x.
Four avian beta-defension prepropeptide cDNA sequences [gallinacins: Gal 1 (synonym CHP 1, chicken heterophil peptide 1), and Gal 2; turkey heterophil peptides: THP 1 and THP 2] were amplified from chicken or turkey bone marrow mRNA samples, respectively. Partial chicken beta-defensin cDNA sequences were obtained using degenerate primers based on chicken peptide sequences (Gal 1/CHP 1 and Gal 2). The complete cDNA sequences of the chicken beta-defensins were then determined by designing specific intrapeptidal primers, from the newly acquired sequence, and pairing one primer with a specific poly A primer tail sequence (3' end) and the other primer with an adapter primer in a 5' rapid amplification of cDNA ends (RACE) reaction. The two, turkey beta-defensins were amplified from turkey marrow using primers designed from chicken beta-defensin preproregions. The complete amino acid sequences for the prepropeptides were deduced for all four avian beta-defensins. Previously, only partial mature peptide sequences for the turkey beta-defensins and complete mature peptide sequences for the chicken beta-defensins were known. All sequences obtained translated accurately to complete and partial amino acid sequences reported for beta-defensins purified from chicken and turkey heterophil granules except for one additional amino acid for Gal 1/CHP 1. The four deduced beta-defensin proregions lack the long, negatively charged propiece reported in classical defensin proregions. These regions are thought to stabilize and inactivate the positively charged mature peptide and target the propeptide to the storage granule. Instead, these beta-defensin proregions are shorter and similar to storage granule-free beta-defensins proregions reported for bovine tracheal antimicrobial peptide (TAP) and lingual antimicrobial peptide (LAP). These are the first prepropeptide beta-defensins from leukocyte granules to be completely characterized.
分别从鸡或火鸡的骨髓mRNA样本中扩增出4条禽β-防御素前原肽cDNA序列[鸡防御素:Gal 1(同义词CHP 1,鸡嗜异性粒细胞肽1)和Gal 2;火鸡嗜异性粒细胞肽:THP 1和THP 2]。基于鸡肽序列(Gal 1/CHP 1和Gal 2)使用简并引物获得部分鸡β-防御素cDNA序列。然后通过从新获得的序列设计特异性肽内引物,并将一个引物与特定的聚腺苷酸引物尾序列(3'端)配对,另一个引物与衔接子引物在5'端cDNA末端快速扩增(RACE)反应中配对,确定鸡β-防御素的完整cDNA序列。使用从鸡β-防御素前原区设计的引物从火鸡骨髓中扩增出两条火鸡β-防御素。推导了所有4种禽β-防御素前原肽的完整氨基酸序列。以前,仅知道火鸡β-防御素的部分成熟肽序列和鸡β-防御素的完整成熟肽序列。除了Gal 1/CHP 1有一个额外的氨基酸外,获得的所有序列均准确翻译为从鸡和火鸡嗜异性粒细胞颗粒中纯化的β-防御素报道的完整和部分氨基酸序列。推导的4种β-防御素原区缺乏经典防御素原区中报道的长的带负电荷的前肽段。这些区域被认为可稳定并使带正电荷的成熟肽失活,并将前肽靶向储存颗粒。相反,这些β-防御素原区较短,类似于报道的牛气管抗菌肽(TAP)和舌抗菌肽(LAP)的无储存颗粒的β-防御素原区。这些是首次完全表征的来自白细胞颗粒的前原肽β-防御素。