Zhang Si-Ming, Loker Eric S
Department of Biology, University of New Mexico, Albuquerque, NM 87131, USA.
Dev Comp Immunol. 2003 Mar;27(3):175-87. doi: 10.1016/s0145-305x(02)00091-5.
Fibrinogen-related proteins (FREPs) found in hemolymph of the snail Biomphalara glabrata are hypothesized to be involved in non-self recognition. Among 150 cloned FREP cDNAs examined, we have identified three additional FREP members, FREPs 3.3, 12.1 and 13.1, bringing the total of FREP subfamilies to 13. The new FREPs each encode two immunoglobulin superfamily domains and a fibrinogen domain. Additionally, five truncated cDNAs with >99% nucleotide identity in coding regions to FREPs 3.2, 12.1 or 13.1 were identified. The truncated forms, the first reported for FREPs, lack a partial exon, one complete exon, or two complete exons plus the 3'UTR. Our preferred hypothesis is that all five truncated cDNAs observed arise from alternative splicing of full-length FREP genes. Genomic sequences lacking at least two introns and corresponding to the 3' ends of the cDNAs of FREP12.1 and its two truncated forms were also recovered. Although these could be the source of the truncated cDNAs, they are believed to be retrosequences.
在光滑双脐螺血淋巴中发现的纤维蛋白原相关蛋白(FREPs)被推测参与非自我识别。在检测的150个克隆的FREP cDNA中,我们又鉴定出三个新的FREP成员,即FREPs 3.3、12.1和13.1,使FREP亚家族总数达到13个。新的FREPs各自编码两个免疫球蛋白超家族结构域和一个纤维蛋白原结构域。此外,还鉴定出五个在编码区与FREPs 3.2、12.1或13.1具有>99%核苷酸同一性的截短cDNA。这些截短形式是首次报道的FREPs,缺少一个部分外显子、一个完整外显子或两个完整外显子加3'UTR。我们倾向的假说是,观察到的所有五个截短cDNA均来自全长FREP基因的可变剪接。还获得了与FREP12.1及其两个截短形式的cDNA 3'端相对应、至少缺少两个内含子的基因组序列。尽管这些可能是截短cDNA的来源,但它们被认为是反转录序列。