Normal Formation of a Subset of Intestinal Granules inCaenorhabditis elegansRequires ATP-binding Cassette Transporters HAF-4 and HAF-9, Which Are Highly Homologous to Human Lysosomal Peptide Transporter TAP-Like

Author:

Kawai Hiromi1,Tanji Takahiro2,Shiraishi Hirohisa2,Yamada Mitsuo1,Iijima Ryoko1,Inoue Takao3,Kezuka Yasuko1,Ohashi Kazuaki1,Yoshida Yasuo4,Tohyama Koujiro4,Gengyo-Ando Keiko5,Mitani Shohei5,Arai Hiroyuki3,Ohashi-Kobayashi Ayako12,Maeda Masatomo1

Affiliation:

1. *Department of Molecular Biology and Biochemistry, Graduate School of Pharmaceutical Sciences, Osaka University, Suita, Osaka 565-0871, Japan;

2. Department of Immunobiology, School of Pharmacy, Iwate Medical University, Yahaba, Shiwa-gun, Iwate 028-3694, Japan;

3. Department of Health Chemistry, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan;

4. The Center for Electron Microscopy and Bio-Imaging Research, Iwate Medical University, Morioka, Iwate 020-8505, Japan; and

5. Department of Physiology, School of Medicine, Tokyo Women's Medical University, Shinjuku-ku, Tokyo 162-8666, Japan

Abstract

TAP-like (TAPL; ABCB9) is a half-type ATP-binding cassette (ABC) transporter that localizes in lysosome and putatively conveys peptides from cytosol to lysosome. However, the physiological role of this transporter remains to be elucidated. Comparison of genome databases reveals that TAPL is conserved in various species from a simple model organism, Caenorhabditis elegans, to mammals. C. elegans possesses homologous TAPL genes: haf-4 and haf-9. In this study, we examined the tissue-specific expression of these two genes and analyzed the phenotypes of the loss-of-function mutants for haf-4 and haf-9 to elucidate the in vivo function of these genes. Both HAF-4 and HAF-9 tagged with green fluorescent protein (GFP) were mainly localized on the membrane of nonacidic but lysosome-associated membrane protein homologue (LMP-1)-positive intestinal granules from larval to adult stage. The mutants for haf-4 and haf-9 exhibited granular defects in late larval and young adult intestinal cells, associated with decreased brood size, prolonged defecation cycle, and slow growth. The intestinal granular phenotype was rescued by the overexpression of the GFP-tagged wild-type protein, but not by the ATP-unbound form of HAF-4. These results demonstrate that two ABC transporters, HAF-4 and HAF-9, are related to intestinal granular formation and some other physiological aspects.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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