研究 elegans 的同源染色体基因近 40 年。

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Development Pub Date : 2024-11-01 Epub Date: 2024-10-30 DOI:10.1242/dev.204328
Paschalis Kratsios, Oliver Hobert
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引用次数: 0

摘要

同源染色体基因是转录因子编码基因中保守性最强的基因家族之一。继在果蝇中发现同源框基因之后,同源框基因又以迅雷不及掩耳之势登上了秀丽隐杆线虫的舞台。1988 年至 1990 年间,也就是在苍蝇和脊椎动物中首次发现同源基因后的短短几年间,定位克隆和基于序列的搜索显示,秀丽隐杆线虫含有 HOX 簇基因,这显然是一个令人惊讶的发现,因为秀丽隐杆线虫的身体结构简单且不分节,而且所有主要亚家族(如 LIM、POU 等)中还有许多其他非簇同源基因。不到 40 年后,我们对同源染色体蛋白在 elegans 中的表达和功能有了非常深入的了解,揭示了它们在神经系统发育中的普遍作用。在本《聚焦》中,我们将从历史的角度对 elegans 同源体领域进行非全面的介绍,并讨论开放性问题和未来发展方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Almost 40 years of studying homeobox genes in C. elegans.

Homeobox genes are among the most deeply conserved families of transcription factor-encoding genes. Following their discovery in Drosophila, homeobox genes arrived on the Caenorhabditis elegans stage with a vengeance. Between 1988 and 1990, just a few years after their initial discovery in flies and vertebrates, positional cloning and sequence-based searches showed that C. elegans contains HOX cluster genes, an apparent surprise given the simplicity and non-segmented body plan of the nematode, as well as many other non-clustered homeobox genes of all major subfamilies (e.g. LIM, POU, etc.). Not quite 40 years later, we have an exceptionally deep understanding of homeodomain protein expression and function in C. elegans, revealing their prevalent role in nervous system development. In this Spotlight, we provide a historical perspective and a non-comprehensive journey through the C. elegans homeobox field and discuss open questions and future directions.

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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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