基因
生物
同源(生物学)
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分子生物学
染色体
重组DNA
基因表达
细胞培养
遗传学
肽序列
作者
Jianjun Wang,Liping Hong,Yi Pan,Shuiping Liu,Kun-Lu Wu,Lijun Tang
出处
期刊:PubMed
日期:2012-01-01
卷期号:37 (1): 27-31
标识
DOI:10.3969/j.issn.1672-7347.2012.01.005
摘要
To explore the down-expression mechanism of MYETS1 gene in multiple myeloma cell lines ARH-77 or KM3, and express MYETS1 gene in prokaryotic express system.The region of chromosome 13q14.3 in ARH-77 and KM3 was detected by FISH. MYETS1 gene was amplified by RT-PCR and cloned into prokaryotic expression vector pGEX-4T.Positive consequence was acquired in 13q14.3 where MYETS1 located by FISH in ARH- 77 and KM3 cell lines. Bioinformatics indicated highly sequence homology between MYETS1 and LECT1, but excluded the homology of open reading frame between MYETS1 and that of LECT1 by RT-PCR. Myets1 protein was expressed and harvested successfully.The region of chromosome 13q14.3 ,where MYETS1 gene located, was not defected in ARH-77 and KM3 cell lines. Down-expression of MYETS1 might be regulated by other mechanisms in multiple myeloma cell lines.
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