Zylstra Paula, Franklin Andrew, Hassan Karl A, Powell Kim L, Steele Edward J, Blanden Robert V
Department of Biological Sciences, The University of Wollongong, Northfields Avenue, NSW 2522, Wollongong, Australia.
Division of Immunology and Genetics, The John Curtin School of Medical Research, Australian National University, PO Box 334, ACT 2601, Canberra, Australia.
Immunogenetics. 2003 Jun;55(3):182-188. doi: 10.1007/s00251-003-0565-x. Epub 2003 May 6.
We have used the polymerase chain reaction (PCR) in an attempt to clone and sequence the exons and hitherto unavailable contiguous flanks of all members of the small V(H) 9 germline gene family from inbred mouse strains and sublines that have had a common ancestry within the last century, and to analyze the molecular evolution of these sequences. Fifteen genuine germline genes were isolated (designated V(H) 9.1 through V(H) 9.15) from strains and sublines of DBA, BALB, 129 and C57BL inbred mice. Of the 15 genuine isolates, nine are novel: seven sequences from DBA strains and sublines ( V(H) 9.3 to V(H) 9.9) and two sequences from C57BL strains ( V(H) 9.13 and V(H) 9.14). We have identified sequencing errors and PCR recombinant artefacts in previously published sequences. We detected no sequence divergence of individual genes shared by the strains and sublines studied. However, we isolated two genes from DBA strains and sublines, V(H) 9.1 and V(H) 9.3, that differ only by five nucleotides encoding three amino acid changes that are concentrated within a 33 nucleotide (11 codon) region. Of these 11 codons, eight encode a putative antigen binding site. There were no differences in the remaining 733 nucleotides sequenced (including both 5' and 3' flanking regions). Potential explanations for the generation of V(H) 9.1 and V(H) 9.3 are discussed.
我们运用聚合酶链反应(PCR),试图从近交系小鼠品系和亚系中克隆并测序小V(H) 9种系基因家族所有成员的外显子及其迄今未知的相邻侧翼序列,这些品系和亚系在过去一个世纪内拥有共同祖先,同时分析这些序列的分子进化。我们从DBA、BALB、129和C57BL近交系小鼠的品系和亚系中分离出15个真正的种系基因(命名为V(H) 9.1至V(H) 9.15)。在这15个真正分离出的基因中,有9个是新发现的:7个序列来自DBA品系和亚系(V(H) 9.3至V(H) 9.9),2个序列来自C57BL品系(V(H) 9.13和V(H) 9.14)。我们在先前发表的序列中发现了测序错误和PCR重组假象。在所研究的品系和亚系共有的单个基因中,我们未检测到序列差异。然而,我们从DBA品系和亚系中分离出两个基因,V(H) 9.1和V(H) 9.3,它们仅相差5个核苷酸,编码3个氨基酸变化,这些变化集中在一个33核苷酸(11个密码子)区域内。在这11个密码子中,有8个编码一个假定的抗原结合位点。在其余测序的733个核苷酸(包括5'和3'侧翼区域)中没有差异。文中讨论了V(H) 9.1和V(H) 9.3产生的可能原因。