TY - JOUR
T1 - Normal formation of a subset of intestinal granules in Caenorhabditis elegans requires ATP-binding cassette transporters HAF-4 and HAF-9, which are highly homologous to human lysosomal peptide transporter TAP-like
AU - Kawai, Hiromi
AU - Tanji, Takahiro
AU - Shiraishi, Hirohisa
AU - Yamada, Mitsuo
AU - Iijima, Ryoko
AU - Inoue, Takao
AU - Kezuka, Yasuko
AU - Ohashi, Kazuaki
AU - Yoshida, Yasuo
AU - Tohyama, Koujiro
AU - Gengyo-Ando, Keiko
AU - Mitani, Shohei
AU - Arai, Hiroyuki
AU - Ohashi-Kobayashi, Ayako
AU - Maeda, Masatomo
PY - 2009/6/15
Y1 - 2009/6/15
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=67449162042&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=67449162042&partnerID=8YFLogxK
U2 - 10.1091/mbc.E08-09-0912
DO - 10.1091/mbc.E08-09-0912
M3 - Article
C2 - 19403699
AN - SCOPUS:67449162042
SN - 1059-1524
VL - 20
SP - 2979
EP - 2990
JO - Molecular Biology of the Cell
JF - Molecular Biology of the Cell
IS - 12
ER -