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鸡IL-15基因的克隆及序列分析

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目的 利用基因工程的方法,将鸡白细胞介素15(ChIL-15)基因在原核表达系统中进行表达,为ChIL-15 的应用提供科学依据.方法 根据美国国家生物信息中心(NCBI)GenBank中已发表的ChIL-15 基因,设计引物,用PCR方法扩增目的基因片段.结果 成功从鸡的脾脏中扩增出含编码区的ChIL-15 基因,ChIL-15 基因为581bp,通过测序进行比对,表明ChIL-15 基因克隆成功.提取的质粒经酶切鉴定、PCR鉴定、测序比对以及编码成氨基酸进行比对均与Gen-Bank中登录号AF139097.1 基本符合,核苷酸的同源性为99.82%.结论 通过使用PCR方法成功扩增出来的ChIL-15基因片段,具有较高的同源性,并与已发表的基因序列相符.这为进一步研究ChIL-15 基因的功能和应用提供了科学依据.
Cloning and sequencing of the gene encoding chicken interleukin-15
Objective To express the chicken interleukin-15(ChIL-15)gene in a prokaryotic expression system by means of genetic engineering to provide a scientific basis for the application of ChIL-15.Methods Primers were designed based on the CHER-15 gene in the GenBank of the National Center for Biological Information(NCBI),and PCR was utilized to amplify the target gene fragment.Result The ChIL-15 gene containing the coding region was successfully amplified from the spleen of chickens,with a length of 581 bp.Sequencing and comparison showed that the ChIL-15 gene was successfully cloned.The extrac-ted plasmids were identified by enzyme digestion,PCR,sequencing,and amino acid coding and were consistent with the registra-tion number AF139097.1 in GenBank.The nucleotide homology was 99.82%.Conclusion The ChIL-15 gene fragment suc-cessfully amplified by the PCR method has high homology and is consistent with the published gene sequence.This provides a scientific basis for further research on the function and application of the ChIL-15 gene.

chickenChIL-15cloningsequence analysis

张凤、田艳花、牛四坤、台晶杰、刘文娟

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山西药科职业学院,山西 太原 030031

ChIL-15 克隆 序列分析

山西药科职业学院院级项目(2023)

2023128

2024

畜禽业
四川省科学技术信息研究所

畜禽业

影响因子:0.15
ISSN:1008-0414
年,卷(期):2024.35(4)
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