| Literature DB >> 33860735 |
Mai E Oguchi1, Yuta Homma1, Mitsunori Fukuda1.
Abstract
We have previously shown that Rab34 is an important regulator of ciliogenesis and that its unique long N-terminal region (amino acids 1-49) is essential for ciliogenesis in certain cultured mammalian cells. In the present study, we performed an in-depth deletion analysis of the N-terminal region of Rab34 together with Ala-based site-directed mutagenesis to identify the essential amino acids that are required for serum-starvation-induced ciliogenesis in hTERT-RPE1 cells. The results showed that a Rab34 mutant lacking an N-terminal 18 amino acids and a Rab34 mutant carrying an LPQ-to-AAA mutation (amino acids 16-18) failed to rescue a Rab34-KO phenotype (i.e., defect in ciliogenesis). Our findings suggest that the LPQ sequence of Rab34 is crucial for ciliogenesis in hTERT-RPE1 cells.Abbreviations: AA, amino acid(s); ac-Tub, acetylated tubulin; bsr, blasticidin S-resistant gene; HRP, horseradish peroxidase; hTERT-RPE1, human telomerase reverse transcriptase retinal pigment epithelium 1; KO, knockout; NS, not significant; PBS, phosphate-buffered saline; puro, puromycin-resistant gene.Entities:
Keywords: Cilia; Rab34; Rab36; ciliary vesicles; ciliogenesis; hTERT-RPE1 cells; membrane traffic; small GTPase
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Year: 2021 PMID: 33860735 PMCID: PMC9122361 DOI: 10.1080/21541248.2021.1894910
Source DB: PubMed Journal: Small GTPases ISSN: 2154-1248