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在活体和计算机模拟中,寻找与缓步动物水熊虫(Ramazzottius varieornatus)的隐生现象相关的CAHS3基因调控基序。

Search for putative gene regulatory motifs in CAHS3, linked to anhydrobiosis in a tardigrade Ramazzottius varieornatus, in vivo and in silico.

作者信息

Ishikawa Sora, Tanaka Sae, Arakawa Kazuharu

机构信息

Institute for Advanced Biosciences, Keio University, Tsuruoka, Japan.

Systems Biology Program, Graduate School of Media and Governance, Keio University, Fujisawa, Japan.

出版信息

Genes Cells. 2024 Dec;29(12):1144-1153. doi: 10.1111/gtc.13168. Epub 2024 Sep 30.

DOI:10.1111/gtc.13168
PMID:39349914
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11609603/
Abstract

Tardigrades possess the ability to enter an almost completely dehydrated state, anhydrobiosis. The CAHS (cytosolic abundant heat-soluble) protein family has been identified as one of the anhydrobiosis-related proteins. In particular, CAHS3 protein from an anhydrobiotic tardigrade, Ramazzottius varieornatus, shows heat-solubility and reversible condensation and is one of the most highly expressed among the CAHS paralogs. A recently developed tardigrade-specific vector showed tissue-specific expression of RvCAHS3 most pronounced in the epidermis in vivo, contrary to the idea that anhydrobiotic genes are uniformly expressed in all tardigrade cells. In this study, we investigated the regulation of RvCAHS3 gene expression through in vivo expression experiments using tardigrade vectors with a series of truncated upstream regions coupled with in silico analysis to identify the anhydrobiosis-related genes that are expressed under the same regulatory system as RvCAHS3. As a result, the 300-350 bp region upstream of RvCAHS3 is critical for regulating gene expression in tardigrade vector experiments, and three motifs conserved between two species of anhydrobiotic tardigrades were identified within a 500 bp region directly upstream of RvCAHS3 start codon. These motifs, which have also been identified upstream of other CAHS genes, could be associated with the regulatory system of anhydrobiosis-related genes in tardigrades.

摘要

缓步动物具有进入几乎完全脱水状态即隐生的能力。CAHS(胞质丰富热溶性)蛋白家族已被确定为与隐生相关的蛋白之一。特别是来自隐生缓步动物水熊虫的CAHS3蛋白,具有热溶性和可逆凝聚性,并且是CAHS旁系同源物中表达量最高的之一。最近开发的一种缓步动物特异性载体显示,RvCAHS3在体内表皮中组织特异性表达最为明显,这与隐生基因在所有缓步动物细胞中均一表达的观点相反。在本研究中,我们通过使用带有一系列截短上游区域的缓步动物载体进行体内表达实验,并结合计算机分析来确定与RvCAHS3在相同调控系统下表达的与隐生相关的基因,从而研究RvCAHS3基因表达的调控。结果表明,在缓步动物载体实验中,RvCAHS3上游300 - 350 bp区域对基因表达调控至关重要,并且在RvCAHS3起始密码子上游500 bp区域内鉴定出了两种隐生缓步动物之间保守的三个基序。这些也在其他CAHS基因上游被鉴定出的基序,可能与缓步动物中与隐生相关基因的调控系统有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a0b/11609603/e6ffb3660703/GTC-29-1144-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a0b/11609603/b7fc93ad51a0/GTC-29-1144-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a0b/11609603/c3244687112a/GTC-29-1144-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a0b/11609603/251d97aa646c/GTC-29-1144-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a0b/11609603/e6ffb3660703/GTC-29-1144-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a0b/11609603/b7fc93ad51a0/GTC-29-1144-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a0b/11609603/c3244687112a/GTC-29-1144-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a0b/11609603/251d97aa646c/GTC-29-1144-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a0b/11609603/e6ffb3660703/GTC-29-1144-g001.jpg

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本文引用的文献

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Proc Jpn Acad Ser B Phys Biol Sci. 2024 Aug 1;100(7):414-428. doi: 10.2183/pjab.pjab.100.023. Epub 2024 Jul 23.
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The Evolution of Temperature and Desiccation-Related Protein Families in Tardigrada Reveals a Complex Acquisition of Extremotolerance.缓步动物门中温度和干燥相关蛋白家族的进化揭示了其对极端环境耐受性的复杂获得过程。
Genome Biol Evol. 2024 Jan 5;16(1). doi: 10.1093/gbe/evad217.
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Nondomain biopolymers: Flexible molecular strategies to acquire biological functions.
非天然生物聚合物:获得生物功能的灵活分子策略。
Genes Cells. 2023 Aug;28(8):539-552. doi: 10.1111/gtc.13050. Epub 2023 May 30.
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In vivo expression vector derived from anhydrobiotic tardigrade genome enables live imaging in Eutardigrada.源自耐干燥缓步动物基因组的活体表达载体使缓步动物在真缓步动物中实现活体成像。
Proc Natl Acad Sci U S A. 2023 Jan 31;120(5):e2216739120. doi: 10.1073/pnas.2216739120. Epub 2023 Jan 24.
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Stress-dependent cell stiffening by tardigrade tolerance proteins that reversibly form a filamentous network and gel.水熊虫耐受蛋白通过形成纤维状网络和凝胶来实现对细胞的应激依赖的刚性变化,该过程是可逆的。
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Insects. 2022 Jun 19;13(6):557. doi: 10.3390/insects13060557.
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