Functional characterisation of LEA proteins from bdelloid rotifers

‘Anhydrobiosis’ or ‘life without water’ is a fascinating phenomenon that was first described by the eminent Dutch microscopist Antony van Leewenhoek in bdelloid rotifers in 1702. Despite being studied for over three hundred years, our understanding of its molecular basis remains largely elusive. Rec...

Full description

Bibliographic Details
Main Author: Tripathi, Rashmi
Published: University of Cambridge 2012
Subjects:
660
Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.571780
id ndltd-bl.uk-oai-ethos.bl.uk-571780
record_format oai_dc
spelling ndltd-bl.uk-oai-ethos.bl.uk-5717802017-12-24T15:13:57ZFunctional characterisation of LEA proteins from bdelloid rotifersTripathi, Rashmi2012‘Anhydrobiosis’ or ‘life without water’ is a fascinating phenomenon that was first described by the eminent Dutch microscopist Antony van Leewenhoek in bdelloid rotifers in 1702. Despite being studied for over three hundred years, our understanding of its molecular basis remains largely elusive. Recently, two group 3 LEA (late embryogenesis abundant) proteins, ArLEA1A and ArLEA1B, have been identified in the desiccation-induced gene set in the bdelloid species Adineta ricciae that are hypothesised to protect these animals by preventing protein aggregation and stabilising membranes respectively. In this dissertation, the functional characteristics of bdelloid LEA proteins have been further explored using computational and experimental tools. Analysis of their phylogeny and domain composition reveals that ArLEA1A and ArLEA1B are evolutionarily distinct from other related group 3 LEA proteins. Moreover, unlike some LEA proteins that are unstructured, bdelloid LEA proteins are predicted to form a-helices, with ArLEA1B having an additional propensity to polymerise into tropomyosin like filaments. These proteins are also predicted to localise in the ER (endoplasmic reticulum) and interact with cell signalling molecules. Intracellular localisation analysis of ArLEA1A and ArLEA1B using confocal microscopy confirms that these proteins translocate into the ER as predicted and their distribution within the entire secretory system and the cell exterior is regulated by their N- and C-terminal signals. Preliminary results suggest that over-expressing ArLEA1A fails to provide protection against protein aggregation within the mammalian ER. Lastly, both ArLEA1A and ArLEA1B are found to provide partial protection against desiccation induced damage of fluorescence properties of the red fluorescent protein mCherry. Overall, the results in this dissertation provide important mechanistic insights into the mode of action of bdelloid LEA proteins during anhydrobiosis.660University of Cambridge10.17863/CAM.16070http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.571780https://www.repository.cam.ac.uk/handle/1810/244584Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 660
spellingShingle 660
Tripathi, Rashmi
Functional characterisation of LEA proteins from bdelloid rotifers
description ‘Anhydrobiosis’ or ‘life without water’ is a fascinating phenomenon that was first described by the eminent Dutch microscopist Antony van Leewenhoek in bdelloid rotifers in 1702. Despite being studied for over three hundred years, our understanding of its molecular basis remains largely elusive. Recently, two group 3 LEA (late embryogenesis abundant) proteins, ArLEA1A and ArLEA1B, have been identified in the desiccation-induced gene set in the bdelloid species Adineta ricciae that are hypothesised to protect these animals by preventing protein aggregation and stabilising membranes respectively. In this dissertation, the functional characteristics of bdelloid LEA proteins have been further explored using computational and experimental tools. Analysis of their phylogeny and domain composition reveals that ArLEA1A and ArLEA1B are evolutionarily distinct from other related group 3 LEA proteins. Moreover, unlike some LEA proteins that are unstructured, bdelloid LEA proteins are predicted to form a-helices, with ArLEA1B having an additional propensity to polymerise into tropomyosin like filaments. These proteins are also predicted to localise in the ER (endoplasmic reticulum) and interact with cell signalling molecules. Intracellular localisation analysis of ArLEA1A and ArLEA1B using confocal microscopy confirms that these proteins translocate into the ER as predicted and their distribution within the entire secretory system and the cell exterior is regulated by their N- and C-terminal signals. Preliminary results suggest that over-expressing ArLEA1A fails to provide protection against protein aggregation within the mammalian ER. Lastly, both ArLEA1A and ArLEA1B are found to provide partial protection against desiccation induced damage of fluorescence properties of the red fluorescent protein mCherry. Overall, the results in this dissertation provide important mechanistic insights into the mode of action of bdelloid LEA proteins during anhydrobiosis.
author Tripathi, Rashmi
author_facet Tripathi, Rashmi
author_sort Tripathi, Rashmi
title Functional characterisation of LEA proteins from bdelloid rotifers
title_short Functional characterisation of LEA proteins from bdelloid rotifers
title_full Functional characterisation of LEA proteins from bdelloid rotifers
title_fullStr Functional characterisation of LEA proteins from bdelloid rotifers
title_full_unstemmed Functional characterisation of LEA proteins from bdelloid rotifers
title_sort functional characterisation of lea proteins from bdelloid rotifers
publisher University of Cambridge
publishDate 2012
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.571780
work_keys_str_mv AT tripathirashmi functionalcharacterisationofleaproteinsfrombdelloidrotifers
_version_ 1718566743666851840