Oncogenomics Unit, CRL-ISPRO, Pisa 56124, Italy.
Institute of Clinical Physiology, CNR, Pisa 56124, Italy.
Biol Open. 2020 Nov 6;9(11):bio053785. doi: 10.1242/bio.053785.
Here, we present miniCoopR-I, an inducible upgrade of the constitutive miniCoopR vector. We developed miniCoopR-I-sponge-204 and miniCoopR-I-pre-miR-204 vectors and we successfully tested them for their ability to achieve time- (embryo/juvenile/adult) and space- (melanocytic lineage) restricted inhibition/overexpression of , a positive modulator of pigmentation previously discovered by us. Furthermore, melanoma-free survival curves performed on induced fish at the adult stage indicate that overexpression accelerates the development of BRAFV600E-driven melanoma. miniCoopR-I allows study of the impact that coding and non-coding modulators of pigmentation exert on melanomagenesis in adult zebrafish, uncoupling it from the impact that they exert on melanogenesis during embryonic development.This article has an associated First Person interview with the first author of the paper.
在这里,我们提出了 miniCoopR-I,这是一个组成型 miniCoopR 载体的诱导型升级。我们开发了 miniCoopR-I-sponge-204 和 miniCoopR-I-pre-miR-204 载体,并成功测试了它们在时间(胚胎/幼年/成年)和空间(黑素细胞谱系)上抑制/过表达 的能力,这是我们之前发现的一种色素沉着的正调节剂。此外,在成年阶段诱导的鱼类上进行的无黑色素瘤存活曲线表明, 过表达加速了 BRAFV600E 驱动的黑色素瘤的发展。miniCoopR-I 允许研究色素沉着的编码和非编码调节剂对成年斑马鱼黑色素瘤发生的影响,将其与它们在胚胎发育过程中对黑素生成的影响分开。本文有一篇与该论文第一作者的第一人称访谈。