[PDF][PDF] Expression of ADP-ribosylation factor (ARF)-like protein 6 during mouse embryonic development

T Takada, K Iida, H Sasaki, M Taira… - International Journal of …, 2005 - ijdb.ehu.es
T Takada, K Iida, H Sasaki, M Taira, H Kimura
International Journal of Developmental Biology, 2005ijdb.ehu.es
ABSTRACT ADP-ribosylation factor (ARF)-like protein 6 (ARL6) is a member of the ARF-like
protein (ARL) subfamily of small GTPases (Moss, 1995; Chavrier, 1999). ARLs are highly
conserved through evolution and most of them possess the consensus sequence required
for GTP binding and hydrolysis (Pasquallato, 2002). Among ARLs, ARL6 which was initially
isolated from a J2E erythroleukemic cell line is divergent in its consensus sequences and its
expression has been shown to be limited to the brain and kidney in adult mouse (Ingley …
ABSTRACT ADP-ribosylation factor (ARF)-like protein 6 (ARL6) is a member of the ARF-like protein (ARL) subfamily of small GTPases (Moss, 1995; Chavrier, 1999). ARLs are highly conserved through evolution and most of them possess the consensus sequence required for GTP binding and hydrolysis (Pasquallato, 2002). Among ARLs, ARL6 which was initially isolated from a J2E erythroleukemic cell line is divergent in its consensus sequences and its expression has been shown to be limited to the brain and kidney in adult mouse (Ingley, 1999). Recently, it was reported that mutations of the ARL6 gene cause type 3 Bardet-Biedl syndrome in humans and that ARL6 is involved in ciliary transport in C. elegans (Chiang, 2004; Fan, 2004). Here, we investigated the expression pattern of ARL6 during early mouse development by whole-mount in situ hybridization and found that interestingly, ARL6 mRNA was localized around the node at 7.0-7.5 days post coitum (dpc) embryos, while weak expression was also found in the ectoderm. At the later stage (8.5 dpc) ARL6 was expressed in the neural plate and probably in the somites. Based on these results, a possible role of ARL6 in early development is discussed in relation to the findings in human and C. elegans (Chiang, 2004; Fan, 2004).
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