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秀丽隐杆线虫含黄素单加氧酶-4在低渗应激的渗透调节中起关键作用。

C. elegans flavin-containing monooxygenase-4 is essential for osmoregulation in hypotonic stress.

作者信息

Hirani Nisha, Westenberg Marcel, Seed Paul T, Petalcorin Mark I R, Dolphin Colin T

机构信息

Institute of Pharmaceutical Science, King's College London, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH, UK.

Division of Women's Health, King's College London, St Thomas' Hospital, London SE1 7EH, UK.

出版信息

Biol Open. 2016 May 15;5(5):537-49. doi: 10.1242/bio.017400.

DOI:10.1242/bio.017400
PMID:27010030
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4874355/
Abstract

Studies in Caenorhabditis elegans have revealed osmoregulatory systems engaged when worms experience hypertonic conditions, but less is known about measures employed when faced with hypotonic stress. Inactivation of fmo-4, which encodes flavin-containing monooxygenase-4, results in dramatic hypoosmotic hypersensitivity; worms are unable to prevent overwhelming water influx and swell rapidly, finally rupturing due to high internal hydrostatic pressure. fmo-4 is expressed prominently in hypodermis, duct and pore cells but is excluded from the excretory cell. Thus, FMO-4 plays a crucial osmoregulatory role by promoting clearance of excess water that enters during hypotonicity, perhaps by synthesizing an osmolyte that acts to establish an osmotic gradient from excretory cell to duct and pore cells. C. elegans FMO-4 contains a C-terminal extension conserved in all nematode FMO-4s. The coincidently numbered human FMO4 also contains an extended C-terminus with features similar to those of FMO-4. Although these shared sequence characteristics suggest potential orthology, human FMO4 was unable to rescue the fmo-4 osmoregulatory defect. Intriguingly, however, mammalian FMO4 is expressed predominantly in the kidney - an appropriate site if it too is, or once was, involved in osmoregulation.

摘要

对秀丽隐杆线虫的研究揭示了线虫在经历高渗条件时所参与的渗透调节系统,但对于其面对低渗应激时所采取的措施了解较少。编码含黄素单加氧酶-4的fmo-4失活会导致显著的低渗超敏反应;线虫无法阻止大量水分涌入,迅速肿胀,最终因内部高静水压力而破裂。fmo-4在皮下组织、管道和孔细胞中显著表达,但排泄细胞中没有。因此,FMO-4可能通过合成一种渗透溶质来建立从排泄细胞到管道和孔细胞的渗透梯度,从而促进在低渗状态下进入的多余水分的清除,在渗透调节中发挥关键作用。秀丽隐杆线虫FMO-4含有一个在所有线虫FMO-4中保守的C端延伸。编号相同的人类FMO4也含有一个与FMO-4具有相似特征的延伸C端。尽管这些共享的序列特征表明可能存在直系同源关系,但人类FMO4无法挽救fmo-4的渗透调节缺陷。然而,有趣的是,哺乳动物FMO4主要在肾脏中表达——如果它也参与或曾经参与渗透调节,这是一个合适的部位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/9bf8a2a42e07/biolopen-5-017400-g7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/25effaa4ed1e/biolopen-5-017400-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/f8f0b0cad746/biolopen-5-017400-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/e4de8d09a22e/biolopen-5-017400-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/a73d9432a622/biolopen-5-017400-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/3ede5fa73e87/biolopen-5-017400-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/da1ea357af2e/biolopen-5-017400-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/9bf8a2a42e07/biolopen-5-017400-g7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/25effaa4ed1e/biolopen-5-017400-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/f8f0b0cad746/biolopen-5-017400-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/e4de8d09a22e/biolopen-5-017400-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/a73d9432a622/biolopen-5-017400-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/3ede5fa73e87/biolopen-5-017400-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/da1ea357af2e/biolopen-5-017400-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/574a/4874355/9bf8a2a42e07/biolopen-5-017400-g7.jpg

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