The ortholog of human solute carrier family 35 member B1 (UDP-galactose transporter-related protein 1) is involved in maintenance of ER homeostasis and essential for larval development in Caenorhabditis elegans

被引:20
作者
Dejima, Katsufumi [1 ,2 ]
Murata, Daisuke [1 ,2 ]
Mizuguchi, Souhei [1 ,2 ]
Nomura, Kazuko H. [1 ,2 ]
Gengyo-Ando, Keiko [2 ,3 ]
Mitani, Shohei [2 ,3 ]
Kamiyama, Shin [4 ]
Nishihara, Shoko [2 ,4 ]
Nomura, Kazuya [1 ,2 ]
机构
[1] Kyushu Univ, Dept Biol, Fac Sci, Fukuoka 8128581, Japan
[2] Japan Sci & Technol Agcy, Saitama, Japan
[3] Tokyo Womens Med Univ, Sch Med, Dept Physiol, Tokyo, Japan
[4] Soka Univ, Fac Engn, Cell Biol Lab, Dept Bioinformat, Tokyo, Japan
关键词
ER stress; RNAi; deletion mutant; glycosylation; model organism; NUCLEOTIDE-SUGAR TRANSPORTERS; ENDOPLASMIC-RETICULUM STRESS; FUNCTIONAL-CHARACTERIZATION; ARABIDOPSIS-THALIANA; MOLECULAR-CLONING; SULFATE SYNTHESIS; GOLGI-APPARATUS; GENE-EXPRESSION; GLUCURONIC ACID; IDENTIFICATION;
D O I
10.1096/fj.08-123737
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although the solute carrier 35B1 (SLC35B1) is evolutionarily conserved, its functions in metazoans remain unknown. To elucidate its function, we examined developmental roles of an SLC35B1 family gene (HUT-1: homolog of UDP-Gal transporter) in Caenorhabditis elegans. We isolated a deletion mutant of the gene and characterized phenotypes of the mutant and hut-1 RNAi-treated worms. GFP-HUT-1 reporter analysis was performed to examine gene expression patterns. We also tested whether several nucleotide sugar transporters can compensate for hut-1 deficiency. The hut-1 deletion mutant and RNAi worms showed larval growth defect and lethality with disrupted intestinal morphology. Inactivation of hut-1 induced chronic endoplasmic reticulum ( ER) stress, and hut-1 showed genetic interactions with the atf-6, pek-1, and ire-1 genes involved in unfolded protein response signaling. ER ultrastructure and ER marker distribution in hut-1-deficient animals showed that HUT-1 is required for maintenance of ER structure. Reporter analysis revealed that HUT- 1 is an ER protein ubiquitously expressed in tissues, including the intestine. Lethality and the ER stress phenotype of the mutant were rescued with the human hut-1 ortholog UGTrel1. These results indicate important roles for hut-1 in development and maintenance of ER homeostasis in C. elegans.-Dejima, K., Murata, D., Mizuguchi, S., Nomura, K. H., Gengyo-Ando, K., Mitani, S., Kamiyama, S., Nishihara, S., Nomura, K. The ortholog of human solute carrier family 35 member B1 (UDP-galactose transporter- related protein 1) is involved in maintenance of ER homeostasis and essential for larval development in Caenorhabditis elegans. FASEB J. 23, 2215-2225 (2009)
引用
收藏
页码:2215 / 2225
页数:11
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