Localisation of a reporter transcript by the c-myc 3′-UTR is linked to translation

被引:5
作者
Dalgleish, GD
Veyrune, JL
Accornero, N
Blanchard, JM
Hesketh, JE [1 ]
机构
[1] Rowett Res Inst, Intracellular Targeting Grp, Aberdeen AB21 9SB, Scotland
[2] CNRS, IGMM, Montpellier, France
关键词
D O I
10.1093/nar/27.22.4363
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The 3'-untranslated region of c-myc mRNA contains a perinuclear localisation signal which is sufficient to target beta-globin coding sequences. The link between perinuclear RNA localisation and translation has been investigated using cells transfected with chimeric gene constructs in which globin reporter sequences were linked to the c-myc 3'-untranslated region and the iron-responsive element from ferritin mRNA. Iron supplementation of the medium promoted translation of the chimeric mRNA as assessed by its presence in polysomes; in situ hybridisation showed that the mRNA was localised around the nucleus. Treatment with the iron chelator desferrioxamine for 16 h prevented both translation and mRNA localisation. In controls where the expressed mRNA lacked the iron-responsive element desferrioxamine had no effect upon localisation. In contrast, arrest of on-going global translation by puromycin treatment had no effect on mRNA localisation. The data suggest that if initiation of translation of a mRNA containing the c-myc localisation signal is prevented in some way then localisation does not occur, whereas once the mRNA has been localised further translation is not required to maintain mRNA localisation.
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页码:4363 / 4368
页数:6
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