Evans Tyler G, Belak Zachery, Ovsenek Nick, Krone Patrick H
Department of Anatomy and Cell Biology, University of Saskatchewan, 107 Wiggins Road, Saskatoon, SK, Canada S7N 5E5.
Comp Biochem Physiol A Mol Integr Physiol. 2007 Jan;146(1):131-40. doi: 10.1016/j.cbpa.2006.09.023. Epub 2006 Oct 6.
Heat shock factors (HSFs) are the major transcription factors responsible for heat-induced upregulation of heat shock protein (Hsp) genes. All three mammalian HSFs (HSF1, HSF2, HSF4) have also been shown to be required for normal mammalian development. It is currently unknown if HSFs play similarly important roles during normal development of non-mammalian vertebrates. In the present study, a morpholino modified antisense oligonucleotide (MO) approach targeted against hsf1 mRNA (hsf1-MO) was used to examine the requirement of HSF1 in zebrafish development. Embryos depleted of HSF1 displayed a reproducible small eye phenotype characterized by an immature lens and a disorganized retinal structure. These defects were strikingly similar to those observed when constitutive, lens specific Hsp70 expression was reduced through the microinjection of MO targeting hsp70. The data suggest that HSF1 is involved in regulating constitutive lens specific expression of hsp70 in the embryonic zebrafish. This conclusion is supported by a marked reduction in Hsp70 protein in hsf1-MO injected embryos. Microinjection of MO targeted to hsf2 mRNA (hsf2-MO) did not result in a small eye phenotype in a significant number of embryos. These data also suggest that HSF1 and HSF2 play distinct roles in non-mammalian vertebrates, similarly to what has been demonstrated previously in mouse.
热休克因子(HSFs)是负责热诱导热休克蛋白(Hsp)基因上调的主要转录因子。所有三种哺乳动物热休克因子(HSF1、HSF2、HSF4)也已被证明是正常哺乳动物发育所必需的。目前尚不清楚热休克因子在非哺乳动物脊椎动物的正常发育过程中是否发挥类似重要的作用。在本研究中,使用针对hsf1 mRNA的吗啉代修饰反义寡核苷酸(MO)方法(hsf1-MO)来检测HSF1在斑马鱼发育中的需求。缺乏HSF1的胚胎表现出可重复的小眼表型,其特征为晶状体不成熟和视网膜结构紊乱。这些缺陷与通过显微注射靶向hsp70的MO降低组成型、晶状体特异性Hsp70表达时观察到的缺陷惊人地相似。数据表明,HSF1参与调节胚胎斑马鱼中hsp70的组成型晶状体特异性表达。这一结论得到了注射hsf1-MO的胚胎中Hsp70蛋白显著减少的支持。显微注射靶向hsf2 mRNA的MO(hsf2-MO)在大量胚胎中未导致小眼表型。这些数据还表明,HSF1和HSF2在非哺乳动物脊椎动物中发挥不同的作用,这与之前在小鼠中所证明的情况类似。