小脑E3连接酶复合物基因在鸡和斑马鱼胚胎对沙利度胺敏感的组织中表达,但在沙利度胺暴露后没有变化

IF 2.5 3区 生物学 Q2 DEVELOPMENTAL BIOLOGY
Lucas Rosa Fraga , Jessica Reeves, Chris Mahony , Lynda Erskine, Neil Vargesson
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引用次数: 0

摘要

沙利度胺是一种臭名昭著的药物,最初被用作镇静剂,直到不幸地发现它具有高度致畸性。尽管如此,它现在被成功地用于治疗一系列临床疾病,包括麻风结节性红斑(ENL)和多发性骨髓瘤(MM)。Cereblon (CRBN)是一种泛素连接酶,是沙利度胺治疗和致畸活性的结合靶点,是CRL4-E3泛素连接酶复合物的一部分,与受损DNA结合蛋白1 (DDB1)和Cullin-4A (CUL4A)蛋白结合。该复合物介导锌指转录因子Ikaros (IKZF1)和Aiolos (IKZF3)的降解,从而介导沙利度胺的抗骨髓瘤反应。为了更好地理解CRBN及其结合伙伴对沙利度胺致畸的重要性,我们分析了野生型和沙利度胺处理的鸡和斑马鱼胚胎中CRBN及其一些已知的E3复合物结合伙伴的表达模式。CRBN和DDB1在整个发育过程中在许多组织中表达,包括那些对沙利度胺敏感的组织,而CUL4A和CRL4-CRBN E3连接酶复合物IKZF1和IKZF3的靶标在不同的时间点表达,并且在体内比CRBN更少的组织中表达。此外,IKZF3在眼组织中表达,而CRBN不表达。然而,尽管我们观察到沙利度胺暴露后鸡蛋黄囊膜血管系统的快速变化,但我们没有检测到蛋黄囊膜血管中CRL4-CRBN E3连接酶复合物的表达。此外,我们在鸡和斑马鱼胚胎中未检测到沙利度胺暴露后CRBN、DDB1、CUL4、IKZF1和IKZF3的表达有任何变化。这些发现表明,沙利度胺的抗血管生成活性可能独立于CRBN而发生,并且沙利度胺在mRNA水平上不调节CRL4-CRBN E3连接酶复合物基因的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cereblon E3 ligase complex genes are expressed in tissues sensitive to thalidomide in chicken and zebrafish embryos but are unchanged following thalidomide exposure

Cereblon E3 ligase complex genes are expressed in tissues sensitive to thalidomide in chicken and zebrafish embryos but are unchanged following thalidomide exposure
Thalidomide is an infamous drug used initially as a sedative until it was tragically discovered it has highly teratogenic properties. Despite this it is now being used to successfully treat a range of clinical conditions including erythema nodosum leprosum (ENL) and multiple myeloma (MM). Cereblon (CRBN), a ubiquitin ligase, is a binding target of thalidomide for both its therapeutic and teratogenic activities and forms part of an CRL4-E3 ubiquitin ligase complex with the proteins Damaged DNA Binding protein 1 (DDB1) and Cullin-4A (CUL4A). This complex mediates degradation of the zinc-finger transcription factors Ikaros (IKZF1) and Aiolos (IKZF3), to mediate thalidomide's anti-myeloma response. To better understand the importance of CRBN and its binding partners for thalidomide teratogenesis here we analysed the expression patterns of CRBN and some of its known E3 complex binding partners in wildtype and thalidomide-treated chicken and zebrafish embryos. CRBN and DDB1 are expressed in many tissues throughout development including those that are thalidomide-sensitive while CUL4A and targets of the CRL4-CRBN E3 Ligase Complex IKZF1 and IKZF3 are expressed at different timepoints and in fewer tissues in the body than CRBN. Furthermore, IKZF3 is expressed in tissues of the eye that CRBN is not. However, although we observed rapid changes to the chicken yolk-sac membrane vasculature following thalidomide exposure, we did not detect CRL4-CRBN E3 Ligase Complex expression in the yolk-sac membrane vessels. Furthermore, we did not detect any changes in CRBN, DDB1, CUL4, IKZF1 and IKZF3 expression following thalidomide exposure in chicken and zebrafish embryos. These findings demonstrate that the anti-angiogenic activities of thalidomide may occur independent of CRBN and that thalidomide does not regulate CRL4-CRBN E3 Ligase Complex gene expression at the mRNA level.
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来源期刊
Developmental biology
Developmental biology 生物-发育生物学
CiteScore
5.30
自引率
3.70%
发文量
182
审稿时长
1.5 months
期刊介绍: Developmental Biology (DB) publishes original research on mechanisms of development, differentiation, and growth in animals and plants at the molecular, cellular, genetic and evolutionary levels. Areas of particular emphasis include transcriptional control mechanisms, embryonic patterning, cell-cell interactions, growth factors and signal transduction, and regulatory hierarchies in developing plants and animals.
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