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一只a2a2兔中的潜在a1 VH种系基因。种系和体细胞水平上基因转换的证据。

Latent a1 VH germline genes in an a2a2 rabbit. Evidence for gene conversion at both the germline and somatic levels.

作者信息

Roux K H, Dhanarajan P, Gottschalk V, McCormick W T, Renshaw R W

机构信息

Department of Biological Science, Florida State University, Tallahassee 32306.

出版信息

J Immunol. 1991 Mar 15;146(6):2027-36.

PMID:1900880
Abstract

We have previously reported the sequences of putative latent a1 cDNA derived from an alpha 2 alpha 2 rabbit. Significant similarity to nominal a1 cDNA sequences was noted, but none of the latent sequences were completely a1-like. We have now probed a genomic library, produced from the same alpha 2 alpha 2 rabbit, for evidence of germline latent a1 VH genes. Four hundred ninety-four VH+ clones were screened with oligonucleotides specific for a1 diagnostic regions of framework region 1 (FR1) and FR3. Twenty-two percent of the VH+ clones hybridized with an a1FR3 oligonucleotide probe. Two a1 FR1 probes yielded weak signals with 6% to 13% of the VH+ clones. Twenty VH genes from clones positive for one or more of the a1-specific oligonucleotide probes were sequenced, revealing 14 unique germline VH genes. All but one of these genes were 85% to 92% identical to the VH1-a1 nominal gene prototype, with sequence identity extending into the leader intron. Most genes displayed extended regions of similarity to a1 in FR1, FR3, or both and expressed 13 to 17 of the 21 allotype-associated residues, consistent with the nominal a1 sequence. The a1-like sequences were variously interspersed with short non-a1 segments, suggestive of germline gene conversion. Although none of the germline a1-like VH genes we have isolated from the alpha 2 alpha 2 rabbits are identical to the known a1 genes or protein sequences from alpha 1 alpha 1 rabbits and 8 of 14 are pseudogenes, most could make significant contributions to the synthesis of a complete nominal a1 sequence by serving as a pool of sequence donors during somatic gene conversion.

摘要

我们之前报道了源自一只α2α2兔子的推定潜伏性a1 cDNA的序列。发现其与标称的a1 cDNA序列有显著相似性,但没有一个潜伏序列完全像a1。我们现在用来自同一只α2α2兔子构建的基因组文库,寻找种系潜伏性a1 VH基因的证据。用针对框架区1(FR1)和FR3的a1诊断区域的寡核苷酸筛选了494个VH+克隆。22%的VH+克隆与a1FR3寡核苷酸探针杂交。两个a1 FR1探针与6%至13%的VH+克隆产生微弱信号。对来自一个或多个a1特异性寡核苷酸探针呈阳性的克隆中的20个VH基因进行了测序,揭示了14个独特的种系VH基因。除了一个基因外,所有这些基因与VH1-a1标称基因原型的同一性为85%至92%,序列同一性延伸至前导内含子。大多数基因在FR1、FR3或两者中显示出与a1相似性的延伸区域,并表达了21个同种异型相关残基中的13至17个,与标称的a1序列一致。a1样序列与短的非a1片段相互穿插,提示种系基因转换。虽然我们从α2α2兔子中分离出的种系a1样VH基因没有一个与α1α1兔子的已知a1基因或蛋白质序列相同,并且14个中有8个是假基因,但大多数基因可以通过在体细胞基因转换过程中作为序列供体库,对完整标称a1序列的合成做出重大贡献。

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