普通的家蜘蛛。

IF 4.1 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Evodevo Pub Date : 2020-03-20 eCollection Date: 2020-01-01 DOI:10.1186/s13227-020-00152-z
Hiroki Oda, Yasuko Akiyama-Oda
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引用次数: 28

摘要

作为节肢动物门螯蛛纲的一种常见的家蛛,从进化的角度研究其发育机制是一个实验系统。本文综述了该生物的特点、主要的研究问题以及现有的主要方法和资源。温斑拟虫的生命周期相对较短,一旦交配,就周期性地产卵。P. tepidariorum胚胎的形态发生场从早期开始就是细胞性的,在进入节肢动物系统型阶段之前,分别表现出与体轴形成和分割相关的逐步对称性破坏事件和条纹形成过程。胚胎场的自我调节能力是白蛉的一个显著特征。在门水平上遗传模式系统的进化机制和逻辑可能是利用这种动物进行研究的主要途径之一。测序的基因组揭示了螯合动物的全基因组重复(WGD),这为研究WGD在动物多样化和进化中的潜在作用提供了一个无脊椎动物平台。谱系特异性器官的发育和进化,包括书肺和吐丝器和丝腺的结合,是有吸引力的研究课题。利用黄颡鱼进行研究可以受益于亲本RNA干扰、显微注射应用(包括细胞标记和胚胎RNA干扰)、多色荧光原位杂交、激光消融以及丰富的基因组和转录组学资源。这些技术使功能基因的发现和揭示细胞和分子的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The common house spider Parasteatoda tepidariorum.

The common house spider Parasteatoda tepidariorum, belonging to the Chelicerata in the phylum Arthropoda, has emerged as an experimental system for studying mechanisms of development from an evolutionary standpoint. In this article, we review the distinct characteristics of P. tepidariorum, the major research questions relevant to this organism, and the available key methods and resources. P. tepidariorum has a relatively short lifecycle and, once mated, periodically lays eggs. The morphogenetic field of the P. tepidariorum embryo is cellular from an early stage and exhibits stepwise symmetry-breaking events and stripe-forming processes that are associated with body axes formation and segmentation, respectively, before reaching the arthropod phylotypic stage. Self-regulatory capabilities of the embryonic field are a prominent feature in P. tepidariorum. The mechanisms and logic underlying the evolvability of heritable patterning systems at the phylum level could be one of the major avenues of research investigated using this animal. The sequenced genome reveals whole genome duplication (WGD) within chelicerates, which offers an invertebrate platform for investigating the potential roles of WGD in animal diversification and evolution. The development and evolution of lineage-specific organs, including the book lungs and the union of spinnerets and silk glands, are attractive subjects of study. Studies using P. tepidariorum can benefit from the use of parental RNA interference, microinjection applications (including cell labeling and embryonic RNA interference), multicolor fluorescence in situ hybridization, and laser ablation as well as rich genomic and transcriptomic resources. These techniques enable functional gene discoveries and the uncovering of cellular and molecular insights.

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来源期刊
Evodevo
Evodevo EVOLUTIONARY BIOLOGY-DEVELOPMENTAL BIOLOGY
CiteScore
7.50
自引率
0.00%
发文量
18
审稿时长
>12 weeks
期刊介绍: EvoDevo publishes articles on a broad range of topics associated with the translation of genotype to phenotype in a phylogenetic context. Understanding the history of life, the evolution of novelty and the generation of form, whether through embryogenesis, budding, or regeneration are amongst the greatest challenges in biology. We support the understanding of these processes through the many complementary approaches that characterize the field of evo-devo. The focus of the journal is on research that promotes understanding of the pattern and process of morphological evolution. All articles that fulfill this aim will be welcome, in particular: evolution of pattern; formation comparative gene function/expression; life history evolution; homology and character evolution; comparative genomics; phylogenetics and palaeontology
期刊最新文献
Early embryonic development of the German cockroach Blattella germanica. Periderm fate and independence of tooth formation are conserved across osteichthyans. Comparative Hox genes expression within the dimorphic annelid Streblospio benedicti reveals patterning variation during development. Single-cell sequencing suggests a conserved function of Hedgehog-signalling in spider eye development. Shared regulatory function of non-genomic thyroid hormone signaling in echinoderm skeletogenesis.
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