The role of toca-1-N-wasp complex in filopodia formation and endocytosis

Transducer of Cdc42 mediated actin polymerization (Toca-1) was identified in 2004 as an essential component of Cdc42 mediated actin polymerization using Xenopus extract. Toca-1 consists of an F-BAR domain at the N-terminal, an HR1 domain (Cdc42 binding site) in the middle and an SH3 domain (N-WASP b...

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Main Author: Bu, Wenyu
Other Authors: Thirumaran s/o Thanabalu
Format: Theses and Dissertations
Language:English
Published: 2010
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Online Access:https://hdl.handle.net/10356/41562
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-415622023-02-28T18:50:44Z The role of toca-1-N-wasp complex in filopodia formation and endocytosis Bu, Wenyu Thirumaran s/o Thanabalu School of Biological Sciences Sohail Ahmed DRNTU::Science::Biological sciences::Molecular biology Transducer of Cdc42 mediated actin polymerization (Toca-1) was identified in 2004 as an essential component of Cdc42 mediated actin polymerization using Xenopus extract. Toca-1 consists of an F-BAR domain at the N-terminal, an HR1 domain (Cdc42 binding site) in the middle and an SH3 domain (N-WASP binding site) at the C-terminal. N-WASP is an activator of actin nucleation through the Arp2/3 complex. Toca-1 or N-WASP induces neurite outgrowth and filopodia formation in N1E115 cells. Toca-1 requires the F-BAR domain, Cdc42 binding site and SH3 domain to induce filopodia. Toca-1 and N-WASP require each other for filopodia formation and synergize to induce filopodia. Toca-1 does not localize in filopodia but is recruited to filopodia by N-WASP. Toca-1 directly interacts with N-WASP in filopodia and Rab5 positive vesicles. Coexpression of Toca-1 and N-WASP affects the distribution and size of Rab5 positive vesicles. Therefore this Toca-1-N-WASP complex not only localizes in filopodia but also induces the formation of filopodia and endocytic vesicles. Three inhibitors of endocytosis, dynamin-K44A, Eps15Δ95/295, and clathrin heavy chain RNAi, block Toca-1 induced filopodia formation. These data suggest that the Toca-1-N-WASP complex can link filopodia formation to endocytosis. The coordinated filopodia formation and endocytosis may be crucial for diverse cellular and developmental processes, such as growth cone guidance and collapse, epithelial cell polarity and border cell migration of Drosophila. Therefore the linkage between filopodia formation and endocytosis may be essential for cellular response to the environmental cues or establishing cell polarity, thus providing a mechanism to coordinate cell signaling events and developmental processes. DOCTOR OF PHILOSOPHY (SBS) 2010-07-21T03:29:21Z 2010-07-21T03:29:21Z 2010 2010 Thesis Bu, W. (2010). The role of toca-1-N-wasp complex in filopodia formation and endocytosis. Doctoral thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/41562 10.32657/10356/41562 en 260 p. application/pdf text/html text/html text/html text/html text/html
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Science::Biological sciences::Molecular biology
spellingShingle DRNTU::Science::Biological sciences::Molecular biology
Bu, Wenyu
The role of toca-1-N-wasp complex in filopodia formation and endocytosis
description Transducer of Cdc42 mediated actin polymerization (Toca-1) was identified in 2004 as an essential component of Cdc42 mediated actin polymerization using Xenopus extract. Toca-1 consists of an F-BAR domain at the N-terminal, an HR1 domain (Cdc42 binding site) in the middle and an SH3 domain (N-WASP binding site) at the C-terminal. N-WASP is an activator of actin nucleation through the Arp2/3 complex. Toca-1 or N-WASP induces neurite outgrowth and filopodia formation in N1E115 cells. Toca-1 requires the F-BAR domain, Cdc42 binding site and SH3 domain to induce filopodia. Toca-1 and N-WASP require each other for filopodia formation and synergize to induce filopodia. Toca-1 does not localize in filopodia but is recruited to filopodia by N-WASP. Toca-1 directly interacts with N-WASP in filopodia and Rab5 positive vesicles. Coexpression of Toca-1 and N-WASP affects the distribution and size of Rab5 positive vesicles. Therefore this Toca-1-N-WASP complex not only localizes in filopodia but also induces the formation of filopodia and endocytic vesicles. Three inhibitors of endocytosis, dynamin-K44A, Eps15Δ95/295, and clathrin heavy chain RNAi, block Toca-1 induced filopodia formation. These data suggest that the Toca-1-N-WASP complex can link filopodia formation to endocytosis. The coordinated filopodia formation and endocytosis may be crucial for diverse cellular and developmental processes, such as growth cone guidance and collapse, epithelial cell polarity and border cell migration of Drosophila. Therefore the linkage between filopodia formation and endocytosis may be essential for cellular response to the environmental cues or establishing cell polarity, thus providing a mechanism to coordinate cell signaling events and developmental processes.
author2 Thirumaran s/o Thanabalu
author_facet Thirumaran s/o Thanabalu
Bu, Wenyu
format Theses and Dissertations
author Bu, Wenyu
author_sort Bu, Wenyu
title The role of toca-1-N-wasp complex in filopodia formation and endocytosis
title_short The role of toca-1-N-wasp complex in filopodia formation and endocytosis
title_full The role of toca-1-N-wasp complex in filopodia formation and endocytosis
title_fullStr The role of toca-1-N-wasp complex in filopodia formation and endocytosis
title_full_unstemmed The role of toca-1-N-wasp complex in filopodia formation and endocytosis
title_sort role of toca-1-n-wasp complex in filopodia formation and endocytosis
publishDate 2010
url https://hdl.handle.net/10356/41562
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