RRC ID 83724
著者 Kuga T, Saraya M, Higuchi S, Yoshida S, Murataka S, Fujiwara Y, Tomita Y, Hayama S, Kaibori Y, Yamagishi N.
タイトル The DUF1669 domain of FAM83H is required for its localization to nuclear speckles.
ジャーナル Sci Rep
Abstract Autosomal-dominant hypocalcified amelogenesis imperfecta (ADHCAI) is caused by mutations in the FAM83H gene. Mutated FAM83H genes encode truncated FAM83H proteins with amino acid lengths between amino acids 1-286 and 1-693, in contrast to wild-type FAM83H (1-1179). Deletion of the C-terminus of FAM83H results in its subcellular translocation from the cytoplasmic compartment to the nuclear speckles, where splicing factors accumulate. However, the amino acid region of FAM83H required for nuclear speckle localization has not yet been determined, and whether all FAM83H-truncated proteins associated with ADHCAI localize to nuclear speckles remains unknown. Here, we examined the subcellular localization of FAM83H mutant proteins with truncations or deletions at various amino acid positions. Deletions within residues 1-300, which corresponds to the DUF1669 domain (17-281), attenuated or abolished the nuclear speckle localization of FAM83H. Meanwhile, some ADHCAI-related FAM83H-truncated proteins did not localize to nuclear speckles, despite the presence of the DUF1669 domain. These results suggest that the DUF1669 domain is required, but not sufficient, for nuclear speckle localization of FAM83H, demonstrating that nuclear speckle localization is not a common feature among FAM83H-truncated proteins related to ADHCAI.
巻・号 15(1)
ページ 12301
公開日 2025-4-10
DOI 10.1038/s41598-025-96356-1
PII 10.1038/s41598-025-96356-1
PMID 40210674
PMC PMC11986100
MeSH Amelogenesis Imperfecta* / genetics Amelogenesis Imperfecta* / metabolism Cell Nucleus* / metabolism Humans Protein Domains Protein Transport Proteins* / chemistry Proteins* / genetics Proteins* / metabolism
IF 3.998
リソース情報
遺伝子材料 IRAK047L06 (HGY019070) IRAK048L18 (HGY019482)