Pick Leslie, Au Kristen
Entomology Department and Graduate Program in Molecular & Cell Biology, 4291 Fieldhouse Drive, University of Maryland, College Park, MD, 20742, USA.
Entomology Department and Graduate Program in Molecular & Cell Biology, 4291 Fieldhouse Drive, University of Maryland, College Park, MD, 20742, USA.
Dev Biol. 2025 Feb;518:1-7. doi: 10.1016/j.ydbio.2024.11.005. Epub 2024 Nov 15.
The discovery that homeotic genes in Drosophila are conserved and utilized for embryonic development throughout the animal kingdom, including humans, revolutionized the fields of developmental biology and evolutionary developmental biology (evo-devo). In a pair of back-to-back papers published in Cell in 1984, researchers at the Biozentrum in Basel, Switzerland, showed that the homeobox - previously identified as a sequence shared by homeotic genes in Drosophila - was also present in the genome of diverse animals. The first paper (McGinnis et al., 1984a) showed that genomes of both invertebrates and vertebrates contain sequences that cross-hybridized with Drosophila homeobox probes. The second paper (Carrasco et al., 1984) identified a cross-hybridizing sequence in the model system Xenopus laevis. They then isolated the first vertebrate homeobox-containing gene by cloning and sequencing of the corresponding genomic region. Finally, they showed that this gene (AC1, later renamed HoxC6) was expressed during embryonic development, the first evidence that developmentally expressed Drosophila genes could be used to isolate regulators of vertebrate embryonic development. These findings led to a flurry of activity in the evo-devo field, initially focused on isolating Hox genes across diverse species, and then expanding to isolation of other gene families based on Drosophila orthologs, an approach that continues today. This led to the notion of a conserved genetic toolkit for embryonic development, currently accepted, but unexpected at the time of its discovery. We attempt to provide some context for the sea-change in thinking that these discoveries brought about by referring to Jean Piaget's theories about the sequential acquisition of scientific knowledge.
果蝇中的同源异型基因在整个动物界(包括人类)的胚胎发育中具有保守性并被利用,这一发现彻底改变了发育生物学和进化发育生物学(evo-devo)领域。在1984年发表于《细胞》杂志的两篇背靠背论文中,瑞士巴塞尔生物中心的研究人员表明,此前被鉴定为果蝇同源异型基因共享序列的同源框,也存在于多种动物的基因组中。第一篇论文(麦金尼斯等人,1984a)表明,无脊椎动物和脊椎动物的基因组都包含与果蝇同源框探针交叉杂交的序列。第二篇论文(卡拉斯科等人,1984)在非洲爪蟾模型系统中鉴定出一个交叉杂交序列。然后,他们通过对相应基因组区域进行克隆和测序,分离出了第一个含有脊椎动物同源框的基因。最后,他们表明这个基因(AC1,后来重新命名为HoxC6)在胚胎发育过程中表达,这是发育中表达的果蝇基因可用于分离脊椎动物胚胎发育调节因子的首个证据。这些发现引发了evo-devo领域的一阵研究热潮,最初集中在跨物种分离Hox基因,然后扩展到基于果蝇直系同源基因分离其他基因家族,这种方法一直延续至今。这导致了一种关于胚胎发育的保守遗传工具包的概念,这一概念目前已被接受,但在其发现之时却出人意料。我们试图通过参考让·皮亚杰关于科学知识顺序获取的理论,为这些发现所带来的思维巨变提供一些背景信息。