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淋巴囊肿病病毒DNA(胞嘧啶-5)甲基转移酶编码基因的鉴定。

Identification of the gene encoding the DNA (cytosine-5) methyltransferase of lymphocystis disease virus.

作者信息

Tidona C A, Schnitzler P, Kehm R, Darai G

机构信息

Institut für Medizinische Virologie der Universität Heidelberg, Federal Republic of Germany.

出版信息

Virus Genes. 1996;12(3):219-29. doi: 10.1007/BF00284642.

Abstract

The gene encoding the DNA (cytosine-5) methyltransferase (m5C-MTase) of lymphocystis disease virus (flounder isolate, LCDV-1) has been identified by polymerase chain reaction (PCR) using oligonucleotide primers synthesized corresponding to different regions of the m5C-MTase gene of frog virus 3 (FV3). A DNA fragment of 487 bp was amplified using oligonucleotide primers L3 and R4 which correspond to the nucleotide positions 87 to 109 and 530 to 550 of the m5C-MTase gene of FV3, respectively. The DNA nucleotide sequence of the PCR product was determined by direct cycle sequencing. The alignment of the deduced amino acid sequence derived from the PCR product and the m5C-MTase protein of FV3 revealed a homology of 55.4% identity and 29.1% similarity. The amino acid sequence which was found to be significantly homologous to the amino acid sequence deduced from the nucleotide sequence of the PCR product was located at the amino acid position 37 to 175 of the m5C-MTase of FV3 indicating the specificity of the amplified PCR product. The DNA nucleotide sequence of the LCDV-1 genome corresponding to the 5' and 3' termini of the m5C-MTase gene was determined by primer walking. The locus of the m5C-MTase gene of LCDV-1 was identified within the EcoRI DNA fragment G of LCDV-1 (7.9 kbp; 0.947 to 0.034 map units). The m5C-MTase gene of LCDV-1 comprises 684 nucleotides coding for a putative protein of 228 amino acid residues. A high degree of amino acid sequence homology (53.3% identity and 25.8% similarity) was detected between the m5C-MTase of LCDV-1 and FV3.

摘要

利用根据蛙病毒3(FV3)的DNA(胞嘧啶-5)甲基转移酶(m5C-MTase)基因不同区域合成的寡核苷酸引物,通过聚合酶链反应(PCR)鉴定了淋巴囊肿病病毒(牙鲆分离株,LCDV-1)编码该酶的基因。使用分别对应于FV3的m5C-MTase基因核苷酸位置87至109和530至550的寡核苷酸引物L3和R4,扩增出一个487 bp的DNA片段。通过直接循环测序确定了PCR产物的DNA核苷酸序列。将PCR产物推导的氨基酸序列与FV3的m5C-MTase蛋白进行比对,结果显示同一性为55.4%,相似性为29.1%。发现与PCR产物核苷酸序列推导的氨基酸序列具有显著同源性的氨基酸序列位于FV3的m5C-MTase的氨基酸位置37至175处,这表明了扩增的PCR产物的特异性。通过引物步移法确定了LCDV-1基因组中与m5C-MTase基因5'和3'末端相对应的DNA核苷酸序列。LCDV-1的m5C-MTase基因定位于LCDV-1的EcoRI DNA片段G(7.9 kbp;0.947至0.034图谱单位)内。LCDV-1的m5C-MTase基因由684个核苷酸组成,编码一个推定的228个氨基酸残基的蛋白质。在LCDV-1和FV3的m5C-MTase之间检测到高度的氨基酸序列同源性(同一性为53.3%,相似性为25.8%)。

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