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

被引:6
作者
Hirani, Nisha [1 ,3 ]
Westenberg, Marcel [1 ,4 ]
Seed, Paul T. [2 ]
Petalcorin, Mark I. R. [1 ,5 ]
Dolphin, Colin T. [1 ]
机构
[1] Kings Coll London, Inst Pharmaceut Sci, Franklin Wilkins Bldg,150 Stamford St, London SE1 9NH, England
[2] Kings Coll London, St Thomas Hosp, Div Womens Hlth, London SE1 7EH, England
[3] Lincolns Inn Fields Labs, Francis Crick Inst, 44 Lincolns Inn Fields, London WC2A 3LY, England
[4] Dutch Natl Plant Protect Org NPPO NL, Natl Reference Ctr, POB 9102, NL-6700 HC Wageningen, Netherlands
[5] Univ Brunei Darussalam, PAPRSB Inst Hlth Sci, Jalan Tungku Link,BE1410, Brunei Muara, Brunei
来源
BIOLOGY OPEN | 2016年 / 5卷 / 05期
基金
英国惠康基金;
关键词
Flavin-containing monooxygenase; FMO-4; C; elegans; Hypotonicity; Osmoregulation; CAENORHABDITIS-ELEGANS; FUNCTIONAL-ANALYSIS; GENE-EXPRESSION; ESCHERICHIA-COLI; MOUSE; FMO; IDENTIFICATION; ENZYMES; EVOLUTION; SEQUENCE;
D O I
10.1242/bio.017400
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:537 / 549
页数:13
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