环己酰亚胺
互补DNA
信使核糖核酸
分子生物学
cDNA文库
北方斑点
生物
克隆(Java方法)
蛋白质生物合成
抑制消减杂交
非翻译区
基因
生物化学
作者
Kai-Shun Chen,Hector F. DeLuca
出处
期刊:Biochimica et biophysica acta (N)
[Elsevier]
日期:1994-09-01
卷期号:1219 (1): 26-32
被引量:310
标识
DOI:10.1016/0167-4781(94)90242-9
摘要
A novel cDNA clone (VDUP1) has been isolated from a cDNA library constructed from mRNA obtained from HL-60 cells stimulated by 1,25-dihydroxyvitamin D-3. Northern blot analysis showed that VDUP1 cDNA hybridizes to a 2.9 kb mRNA species which is up-regulated in HL-60 cells by 1,25-dihydroxyvitamin D-3 (1,25-(OH)2D3) treatment. In vitro expression of VDUP1 cDNA produced a 46 kDa protein. A search of the GenBank database revealed that the 3′ untranslated region of VDUP1 is homologous to a sequence expressed in brain. A detailed time course study showed that the VDUP1 mRNA starts to increase at 6 h after 1,25-dihydroxyvitamin D-3 treatment, reaches a plateau at around 18 h and stays elevated for 24 h. The VDUP1 mRNA is not regulated by phorbol 12-myristate 13-acetate (PMA) in HL-60 cells. Inhibition of protein synthesis by cycloheximide does not prevent the induction of VDUP1 mRNA by 1,25-dihydroxyvitamin D-3. Cycloheximide itself increases VDUP1 mRNA levels. These results suggest that the degradation of VDUP1 mRNA is either translation-dependent or regulated by a labile protein.
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