Functional analysis of WASP and Las17p using Saccharomyces cerevisiae las17Δ cells

Wiskott Aldrich Syndrome (WAS) is a genetic disease caused by recessive mutations in the gene encoding the Wiskott Aldrich Syndrome protein (WASP). Patients suffering from WAS exhibit a variety of symptoms ranging from thrombocytopenia, eczema and immune disorders. WASP belongs to a family of protei...

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Bibliographic Details
Main Author: Raj Mohan Raja Muthiah
Other Authors: Thirumaran s/o Thanabalu
Format: Thesis
Language:English
Published: 2009
Subjects:
Online Access:https://hdl.handle.net/10356/20683
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author Raj Mohan Raja Muthiah
author2 Thirumaran s/o Thanabalu
author_facet Thirumaran s/o Thanabalu
Raj Mohan Raja Muthiah
author_sort Raj Mohan Raja Muthiah
collection NTU
description Wiskott Aldrich Syndrome (WAS) is a genetic disease caused by recessive mutations in the gene encoding the Wiskott Aldrich Syndrome protein (WASP). Patients suffering from WAS exhibit a variety of symptoms ranging from thrombocytopenia, eczema and immune disorders. WASP belongs to a family of proteins whose members include WASP, N-WASP, WAVEI-3 and Lasl7p. WASP has a WH1 domain at the N-terminus and the Arp213 complex activating VCA domain at the C-terminus. WASP is expressed predominantly in hematopoietic cells and is involved in integrating extracellular signals and regulating actin cytoskeleton. Lasl7p is the S. cerevisiae ortholog of mammalian WASP and has a similar domain structure as that of WASP. Deletion or mutation in the gene encoding Lasl7p makes the yeast cells inviable at restrictive temperatures and also causes defects in endocytosis and actin patch polarization at all temperatures.
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spelling ntu-10356/206832023-02-28T18:34:35Z Functional analysis of WASP and Las17p using Saccharomyces cerevisiae las17Δ cells Raj Mohan Raja Muthiah Thirumaran s/o Thanabalu School of Biological Sciences DRNTU::Science::Biological sciences Wiskott Aldrich Syndrome (WAS) is a genetic disease caused by recessive mutations in the gene encoding the Wiskott Aldrich Syndrome protein (WASP). Patients suffering from WAS exhibit a variety of symptoms ranging from thrombocytopenia, eczema and immune disorders. WASP belongs to a family of proteins whose members include WASP, N-WASP, WAVEI-3 and Lasl7p. WASP has a WH1 domain at the N-terminus and the Arp213 complex activating VCA domain at the C-terminus. WASP is expressed predominantly in hematopoietic cells and is involved in integrating extracellular signals and regulating actin cytoskeleton. Lasl7p is the S. cerevisiae ortholog of mammalian WASP and has a similar domain structure as that of WASP. Deletion or mutation in the gene encoding Lasl7p makes the yeast cells inviable at restrictive temperatures and also causes defects in endocytosis and actin patch polarization at all temperatures. DOCTOR OF PHILOSOPHY (SBS) 2009-12-23T07:06:03Z 2009-12-23T07:06:03Z 2008 2008 Thesis Raj, M. R. M. (2008). Functional analysis of WASP and Las17p using saccharomyces cerevisiae las17Δ cells. Doctoral thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/20683 10.32657/10356/20683 en 244 p. application/pdf
spellingShingle DRNTU::Science::Biological sciences
Raj Mohan Raja Muthiah
Functional analysis of WASP and Las17p using Saccharomyces cerevisiae las17Δ cells
title Functional analysis of WASP and Las17p using Saccharomyces cerevisiae las17Δ cells
title_full Functional analysis of WASP and Las17p using Saccharomyces cerevisiae las17Δ cells
title_fullStr Functional analysis of WASP and Las17p using Saccharomyces cerevisiae las17Δ cells
title_full_unstemmed Functional analysis of WASP and Las17p using Saccharomyces cerevisiae las17Δ cells
title_short Functional analysis of WASP and Las17p using Saccharomyces cerevisiae las17Δ cells
title_sort functional analysis of wasp and las17p using saccharomyces cerevisiae las17δ cells
topic DRNTU::Science::Biological sciences
url https://hdl.handle.net/10356/20683
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