Related Experiment Video
Updated: Mar 3, 2026

Observation of the Ciliary Movement of Choroid Plexus Epithelial Cells Ex Vivo
Published on: July 13, 2015
The Ciliary Protein IFT57 in the Macronucleus of Paramecium
Lei Shi1,2, France Koll1, Olivier Arnaiz1
1Institute for Integrative Biology of the Cell (I2BC), formerly Centre de Génétique Moléculaire, Université Paris Saclay, CEA, CNRS, 1 Avenue de la Terrasse, 91198, Gif sur Yvette, France.
Abstract:
The intraflagellar transport IFT57 protein is essential for ciliary growth and maintenance. Also known as HIPPI, human IFT57 can be translocated to the nucleus via a molecular partner of the Huntingtin, Hip1, inducing gene expression changes. In Paramecium tetraurelia, we identified four IFT57 genes forming two subfamilies IFT57A/B and IFT57C/D arising from whole genome duplications. The depletion of proteins of the two subfamilies induced ciliary defects and IFT57A and IFT57C localized in basal bodies and cilia. We observed that IFT57A, but not IFT57C, is also present in the macronucleus and able to traffic toward the developing anlage during autogamy. Analysis of chimeric IFT57A-IFT57C-GFP-tagged proteins allowed us to identify a region of IFT57A necessary for nuclear localization. We studied the localization of the unique IFT57 protein of Paramecium caudatum, a species, which diverged from P. tetraurelia before the whole genome duplications. The P. caudatumIFT57C protein was excluded from the nucleus. We also analyzed whether the overexpression of IFT57A in Paramecium could affect gene transcription as the human protein does in HeLa cells. The expression of some genes was indeed affected by overexpression of IFT57A, but the set of affected genes poorly overlaps the set of genes affected in human cells.
Insights
Intraflagellar transport IFT57 proteins are crucial for cilia. In Paramecium, IFT57A localizes to the nucleus and influences gene expression, unlike IFT57C, with distinct functions across species.
Area of Science:
- Cell Biology
- Genetics
- Molecular Biology
Background:
- Intraflagellar transport (IFT) proteins, like IFT57, are vital for ciliary assembly and function.
- Human IFT57 (HIPPI) translocates to the nucleus, modulating gene expression.
- Paramecium tetraurelia possesses multiple IFT57 gene copies due to whole genome duplication.
Purpose of the Study:
- To investigate the distinct roles and localization of IFT57 paralogs in Paramecium.
- To identify the nuclear localization signals within IFT57A.
- To compare the gene regulatory effects of Paramecium IFT57A with human IFT57.
Main Methods:
- Gene depletion and protein localization studies in Paramecium.
- Analysis of chimeric IFT57A-IFT57C-GFP fusion proteins.
- Comparative analysis of IFT57 protein from Paramecium species with different evolutionary histories.
- Gene expression profiling following IFT57A overexpression.
Main Results:
- Paramecium IFT57 proteins form two subfamilies (IFT57A/B and IFT57C/D), with depletion causing ciliary defects.
- IFT57A localizes to basal bodies, cilia, and the macronucleus, trafficking during autogamy.
- A specific region of IFT57A mediates nuclear import.
- Paramecium caudatum IFT57C is excluded from the nucleus.
- Overexpression of IFT57A affects some gene expression in Paramecium, but with limited overlap to human cells.
Conclusions:
- Paramecium IFT57 paralogs exhibit divergent localization and functions, with IFT57A possessing nuclear activity.
- Evolutionary divergence and whole genome duplication have shaped IFT57 gene families.
- While IFT57A influences gene expression in Paramecium, its targets differ from human HIPPI, suggesting species-specific regulatory roles.
Related Concept Videos
Microtubules in Cell Motility
Microtubules in Signaling
Mechanism of Ciliary Motion
The cilia are made up of microtubules in a 9+2 arrangement, with nine microtubule doublet ring bundles, surrounding a pair of central singlet microtubule bundles. The doublet microtubule bundles are...
Microtubule Associated Motor Proteins
Histone Variants at the Centromere
Mechanism of Filopodia Formation
Their main function is to guide migrating cells during normal tissue morphogenesis or cancer metastasis by recognizing and making initial contacts with the extracellular matrix. However, they can also act as stationary cell anchors or help to establish communication...

