Hench Jürgen, Henriksson Johan, Abou-Zied Akram M, Lüppert Martin, Dethlefsen Johan, Mukherjee Krishanu, Tong Yong Guang, Tang Lois, Gangishetti Umesh, Baillie David L, Bürglin Thomas R
Dept. of Biosciences and Nutrition & Center for Biosciences, Karolinska Institutet, Hälsovägen 7, Novum, SE-141 83, Huddinge, Sweden; School of Life Sciences, Södertörns Högskola, Huddinge, Sweden.
Dept. of Biosciences and Nutrition & Center for Biosciences, Karolinska Institutet, Hälsovägen 7, Novum, SE-141 83, Huddinge, Sweden.
PLoS One. 2015 May 29;10(5):e0126947. doi: 10.1371/journal.pone.0126947. eCollection 2015.
Homeobox genes play crucial roles for the development of multicellular eukaryotes. We have generated a revised list of all homeobox genes for Caenorhabditis elegans and provide a nomenclature for the previously unnamed ones. We show that, out of 103 homeobox genes, 70 are co-orthologous to human homeobox genes. 14 are highly divergent, lacking an obvious ortholog even in other Caenorhabditis species. One of these homeobox genes encodes 12 homeodomains, while three other highly divergent homeobox genes encode a novel type of double homeodomain, termed HOCHOB. To understand how transcription factors regulate cell fate during development, precise spatio-temporal expression data need to be obtained. Using a new imaging framework that we developed, Endrov, we have generated spatio-temporal expression profiles during embryogenesis of over 60 homeobox genes, as well as a number of other developmental control genes using GFP reporters. We used dynamic feedback during recording to automatically adjust the camera exposure time in order to increase the dynamic range beyond the limitations of the camera. We have applied the new framework to examine homeobox gene expression patterns and provide an analysis of these patterns. The methods we developed to analyze and quantify expression data are not only suitable for C. elegans, but can be applied to other model systems or even to tissue culture systems.
同源异型框基因在多细胞真核生物的发育过程中发挥着关键作用。我们生成了一份秀丽隐杆线虫所有同源异型框基因的修订列表,并为之前未命名的基因提供了命名法。我们发现,在103个同源异型框基因中,有70个与人的同源异型框基因是直系同源基因。14个基因高度分化,即使在其他秀丽隐杆线虫物种中也缺乏明显的直系同源基因。其中一个同源异型框基因编码12个同源异型结构域,而其他三个高度分化的同源异型框基因编码一种新型的双同源异型结构域,称为HOCHOB。为了了解转录因子在发育过程中如何调控细胞命运,需要获得精确的时空表达数据。利用我们开发的新成像框架Endrov,我们使用绿色荧光蛋白(GFP)报告基因生成了60多个同源异型框基因以及一些其他发育控制基因在胚胎发育过程中的时空表达谱。我们在记录过程中使用动态反馈自动调整相机曝光时间,以扩大动态范围,突破相机的限制。我们应用这个新框架来检查同源异型框基因的表达模式,并对这些模式进行分析。我们开发的用于分析和量化表达数据的方法不仅适用于秀丽隐杆线虫,还可应用于其他模型系统甚至组织培养系统。