Modular control of vertebrate axis segmentation in time and space.

IF 9.4 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
EMBO Journal Pub Date : 2024-09-01 Epub Date: 2024-08-09 DOI:10.1038/s44318-024-00186-2
Ali Seleit, Ian Brettell, Tomas Fitzgerald, Carina Vibe, Felix Loosli, Joachim Wittbrodt, Kiyoshi Naruse, Ewan Birney, Alexander Aulehla
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引用次数: 0

Abstract

How the timing of development is linked to organismal size is a longstanding question. Although numerous studies have reported a correlation of temporal and spatial traits, the developmental or selective constraints underlying this link remain largely unexplored. We address this question by studying the periodic process of embryonic axis segmentation in-vivo in Oryzias fish. Interspecies comparisons reveal that the timing of segmentation correlates to segment, tissue and organismal size. Segment size in turn scales according to tissue and organism size. To probe for underlying causes, we genetically hybridised two closely related species. Quantitative analysis in ~600 phenotypically diverse F2 embryos reveals a decoupling of timing from size control, while spatial scaling is preserved. Using developmental quantitative trait loci (devQTL) mapping we identify distinct genetic loci linked to either the control of segmentation timing or tissue size. This study demonstrates that a developmental constraint mechanism underlies spatial scaling of axis segmentation, while its spatial and temporal control are dissociable modules.

脊椎动物轴分节在时间和空间上的模块化控制
发育时间如何与生物体大小相关是一个长期存在的问题。尽管许多研究都报道了时间和空间特征的相关性,但这一联系背后的发育或选择性制约因素在很大程度上仍未得到探讨。为了解决这个问题,我们研究了鹗鱼体内胚胎轴分节的周期性过程。种间比较显示,轴的分节时间与分节、组织和生物体的大小相关。节段大小又与组织和生物体大小相关。为了探究其根本原因,我们对两个密切相关的物种进行了基因杂交。对大约 600 个表型不同的 F2 胚胎进行的定量分析显示,时间与大小控制脱钩,而空间比例保持不变。利用发育定量性状位点(devQTL)图谱,我们确定了与分割时间控制或组织大小控制相关的不同遗传位点。这项研究表明,轴分割的空间缩放是发育约束机制的基础,而其空间和时间控制则是可分离的模块。
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来源期刊
EMBO Journal
EMBO Journal 生物-生化与分子生物学
CiteScore
18.90
自引率
0.90%
发文量
246
审稿时长
1.5 months
期刊介绍: The EMBO Journal has stood as EMBO's flagship publication since its inception in 1982. Renowned for its international reputation in quality and originality, the journal spans all facets of molecular biology. It serves as a platform for papers elucidating original research of broad general interest in molecular and cell biology, with a distinct focus on molecular mechanisms and physiological relevance. With a commitment to promoting articles reporting novel findings of broad biological significance, The EMBO Journal stands as a key contributor to advancing the field of molecular biology.
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