Mendoza-García Patricia, Hugosson Fredrik, Fallah Mahsa, Higgins Michael L, Iwasaki Yasuno, Pfeifer Kathrin, Wolfstetter Georg, Varshney Gaurav, Popichenko Dmitry, Gergen J Peter, Hens Korneel, Deplancke Bart, Palmer Ruth H
Department of Medical Biochemistry and Cell Biology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Molecular Biology, Umeå University, Umeå, Sweden.
PLoS Genet. 2017 Apr 3;13(4):e1006617. doi: 10.1371/journal.pgen.1006617. eCollection 2017 Apr.
The Anaplastic Lymphoma Kinase (Alk) receptor tyrosine kinase (RTK) plays a critical role in the specification of founder cells (FCs) in the Drosophila visceral mesoderm (VM) during embryogenesis. Reporter gene and CRISPR/Cas9 deletion analysis reveals enhancer regions in and upstream of the Alk locus that influence tissue-specific expression in the amnioserosa (AS), the VM and the epidermis. By performing high throughput yeast one-hybrid screens (Y1H) with a library of Drosophila transcription factors (TFs) we identify Odd-paired (Opa), the Drosophila homologue of the vertebrate Zic family of TFs, as a novel regulator of embryonic Alk expression. Further characterization identifies evolutionarily conserved Opa-binding cis-regulatory motifs in one of the Alk associated enhancer elements. Employing Alk reporter lines as well as CRISPR/Cas9-mediated removal of regulatory elements in the Alk locus, we show modulation of Alk expression by Opa in the embryonic AS, epidermis and VM. In addition, we identify enhancer elements that integrate input from additional TFs, such as Binou (Bin) and Bagpipe (Bap), to regulate VM expression of Alk in a combinatorial manner. Taken together, our data show that the Opa zinc finger TF is a novel regulator of embryonic Alk expression.
间变性淋巴瘤激酶(Alk)受体酪氨酸激酶(RTK)在果蝇胚胎发育期间的内脏中胚层(VM)中前体细胞(FCs)的特化过程中起着关键作用。报告基因和CRISPR/Cas9缺失分析揭示了Alk基因座内部及其上游的增强子区域,这些区域影响浆膜(AS)、VM和表皮中的组织特异性表达。通过用果蝇转录因子(TFs)文库进行高通量酵母单杂交筛选(Y1H),我们鉴定出Odd-paired(Opa),即脊椎动物锌指蛋白家族TFs的果蝇同源物,作为胚胎Alk表达的一种新型调节因子。进一步的表征在其中一个Alk相关增强子元件中鉴定出进化保守的Opa结合顺式调节基序。利用Alk报告系以及CRISPR/Cas9介导的Alk基因座中调节元件的去除,我们展示了Opa在胚胎AS、表皮和VM中对Alk表达的调节作用。此外,我们鉴定出增强子元件,这些元件整合了来自其他TFs(如Binou(Bin)和Bagpipe(Bap))的输入,以组合方式调节Alk在VM中的表达。综上所述,我们的数据表明Opa锌指TF是胚胎Alk表达的一种新型调节因子。