Profiling truncated variants of TCTN1 unveils the essential role of its integrity for ciliogenesis

Cilia protrude from the cell surface to execute signal transduction and cell motility. Tectonic (TCTN) is a transition-zone (TZ) "gatekeeper" that determines ciliary composition and function. The role of its only conserved module in the TCTN protein family, DUF1619, lacks functional annotation. Herein, we quantitatively compared full-length TCTN1 and four truncations (DUF1619, ΔDUF1619, N-DUF1619, and DUF1619-C) stably expressed in <i>Chlamydomonas reinhardtii tctn1</i> cells. Surprisingly, neither fragment could rescue ciliary morphology of <i>tctn1</i>; DUF1619 alone aggravates ciliary defects. In particular, deletion of either terminus decreases TZ localization and, for the C-terminus, destabilizes the protein during ciliary disassembly. Thus, our findings demonstrate that the full-length TCTN1, rather than DUF1619 alone, is indispensable for ciliary integrity.

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Journal
iScience
Published
2025-11-24
DOI
https://doi.org/10.1016/j.isci.2025.114190
Primary Topic
Genetic and Kidney Cyst Diseases
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article
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article

Profiling truncated variants of TCTN1 unveils the essential role of its integrity for ciliogenesis

Suhui Wang, Zhihui Dong, Lin Jiang, Qian Yi et al.
iScience
Genetic and Kidney Cyst Diseases
article

Profiling truncated variants of TCTN1 unveils the essential role of its integrity for ciliogenesis

Suhui Wang, Zhihui Dong, Lin Jiang, Qian Yi, Ya Li, Liang Wang, Yunkun Wu, Huimin Yu, Zhao Ma, Chuang Xu, Chenyu Miao
article en

Abstract

Cilia protrude from the cell surface to execute signal transduction and cell motility. Tectonic (TCTN) is a transition-zone (TZ) "gatekeeper" that determines ciliary composition and function. The role of its only conserved module in the TCTN protein family, DUF1619, lacks functional annotation. Herein, we quantitatively compared full-length TCTN1 and four truncations (DUF1619, ΔDUF1619, N-DUF1619, and DUF1619-C) stably expressed in <i>Chlamydomonas reinhardtii tctn1</i> cells. Surprisingly, neither fragment could rescue ciliary morphology of <i>tctn1</i>; DUF1619 alone aggravates ciliary defects. In particular, deletion of either terminus decreases TZ localization and, for the C-terminus, destabilizes the protein during ciliary disassembly. Thus, our findings demonstrate that the full-length TCTN1, rather than DUF1619 alone, is indispensable for ciliary integrity.

iScienceVol. 28(12)
Jiangsu Normal University (CN)
Openalex Percentile: Top 62%
Genetic and Kidney Cyst Diseases
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