首页> 外文期刊>西安医科大学学报(英文版) >STUDY OF ECK GENE EXON-3 FROM HUMAN NORMAL TISSUE AND BREAST CANCER CELL LINE
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STUDY OF ECK GENE EXON-3 FROM HUMAN NORMAL TISSUE AND BREAST CANCER CELL LINE

机译:人体正常组织和乳腺癌细胞株中ECK基因exon-3的研究

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Objective To establish a method cloning the exon 3 of eck gene from normal tissue and ZR-75-1 cell line (a human breast cancer cell line)and study whether these genes exist mutant. Methods Designed a pair of specific primers and amplified the exon 3 of eck gene fragment from the extracted genomic DNA derived from normal epithelial cells from skin tissue and ZR-75-1 cell line respectively by PCR technique. Transformed the E.coil. JM109 with recombinant plamids constructed by inserting the amplified fragments into medium vector pUCm-T and sequenced these amplified fragments after primary screening of endonuclease restriction digestion and PCR amplification. Results ① Obtained the genomic DNA of human normal epithelial cells and ZR-75-1 cell line respectively. ② Obtained the amplified fragments of human exon 3 of eck gene through PCR technique. ③ Obtained the cloning vectors of exon 3 of eck gene of human normal epithelial cells and ZR-75-1 cell line respectively. ④ ZR-75-1 cell line exists mutation of nucleotides. Conclusion Successfully established the method of cloning the human exon 3 of eck gene and found some mutations in the detected samples. This study lays a foundation for further studying the function of eck gene in tumorgenesis.
机译:目的建立一种从正常组织和人乳腺癌细胞ZR-75-1细胞系中克隆eck基因外显子3的方法,并研究这些基因是否存在突变体。方法设计一对特异性引物,通过PCR技术分别从皮肤组织和ZR-75-1细胞系正常上皮细胞提取的基因组DNA中扩增eck基因片段的外显子3。改造了电子线圈。通过将扩增的片段插入培养基载体pUCm-T中并在对核酸内切酶限制性消化和PCR扩增进行初步筛选后对这些扩增的片段进行测序而构建的重组质粒的JM109。结果①分别获得人正常上皮细胞和ZR-75-1细胞株的基因组DNA。 ②通过PCR技术获得了eck基因人3号外显子的扩增片段。 ③分别获得人正常上皮细胞eck基因外显子3和ZR-75-1细胞株的克隆载体。 ④ZR-75-1细胞系存在核苷酸突变。结论成功建立了eck基因人类外显子3的克隆方法,并在检测到的样品中发现了一些突变。该研究为进一步研究eck基因在肿瘤发生中的功能奠定了基础。

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