Literature DB >> 10212148

A functional analysis of inscuteable and its roles during Drosophila asymmetric cell divisions.

M Tio1, M Zavortink, X Yang, W Chia.   

Abstract

Cellular diversity in the Drosophila central nervous system is generated through a series of asymmetric cell divisions in which one progenitor produces two daughter cells with distinct fates. Asymmetric basal cortical localisation and segregation of the determinant Prospero during neuroblast cell divisions play a crucial role in effecting distinct cell fates for the progeny sibling neuroblast and ganglion mother cell. Similarly asymmetric localisation and segregation of the determinant Numb during ganglion mother cell divisions ensure that the progeny sibling neurons attain distinct fates. The most upstream component identified so far which acts to organise both neuroblast and ganglion mother cell asymmetric divisions is encoded by inscuteable. The Inscuteable protein is itself asymmetrically localised to the apical cell cortex and is required both for the basal localisation of the cell fate determinants during mitosis and for the orientation of the mitotic spindle along the apical/basal axis. Here we define the functional domains of Inscuteable. We show that aa252-578 appear sufficient to effect all aspects of its function, however, the precise requirements for its various functions differ. The region, aa288-497, is necessary and sufficient for apical cortical localisation and for mitotic spindle (re)orientation along the apical/basal axis. A larger region aa288-540 is necessary and sufficient for asymmetric Numb localisation and segregation; however, correct localisation of Miranda and Prospero requires additional sequences from aa540-578. The requirement for the resolution of distinct sibling neuronal fates appears to coincide with the region necessary and sufficient for Numb localisation (aa288-540). Our data suggest that apical localisation of the Inscuteable protein is a necessary prerequisite for all other aspects of its function. Finally, we show that although inscuteable RNA is normally apically localised, RNA localisation is not required for protein localisation or any aspects of inscuteable function.

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Year:  1999        PMID: 10212148     DOI: 10.1242/jcs.112.10.1541

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  9 in total

1.  Structural basis for interaction between the conserved cell polarity proteins Inscuteable and Leu-Gly-Asn repeat-enriched protein (LGN).

Authors:  Satoru Yuzawa; Sachiko Kamakura; Yuko Iwakiri; Junya Hayase; Hideki Sumimoto
Journal:  Proc Natl Acad Sci U S A       Date:  2011-11-10       Impact factor: 11.205

2.  Drosophila homologs of mammalian TNF/TNFR-related molecules regulate segregation of Miranda/Prospero in neuroblasts.

Authors:  Huashan Wang; Yu Cai; William Chia; Xiaohang Yang
Journal:  EMBO J       Date:  2006-11-30       Impact factor: 11.598

3.  Membrane targeting and asymmetric localization of Drosophila partner of inscuteable are discrete steps controlled by distinct regions of the protein.

Authors:  Fengwei Yu; Chin Tong Ong; William Chia; Xiaohang Yang
Journal:  Mol Cell Biol       Date:  2002-06       Impact factor: 4.272

Review 4.  Going vertical: functional role and working principles of the protein Inscuteable in asymmetric cell divisions.

Authors:  Simone Culurgioni; Marina Mapelli
Journal:  Cell Mol Life Sci       Date:  2013-03-21       Impact factor: 9.261

5.  Inscuteable regulates the Pins-Mud spindle orientation pathway.

Authors:  Jonathon F Mauser; Kenneth E Prehoda
Journal:  PLoS One       Date:  2012-01-10       Impact factor: 3.240

Review 6.  The GAPs, GEFs, and GDIs of heterotrimeric G-protein alpha subunits.

Authors:  David P Siderovski; Francis S Willard
Journal:  Int J Biol Sci       Date:  2005-04-01       Impact factor: 6.580

7.  Maintenance of Miranda Localization in Drosophila Neuroblasts Involves Interaction with the Cognate mRNA.

Authors:  Anne Ramat; Matthew Hannaford; Jens Januschke
Journal:  Curr Biol       Date:  2017-07-06       Impact factor: 10.834

8.  Insc:LGN tetramers promote asymmetric divisions of mammary stem cells.

Authors:  Simone Culurgioni; Sara Mari; Paola Bonetti; Sara Gallini; Greta Bonetto; Martha Brennich; Adam Round; Francesco Nicassio; Marina Mapelli
Journal:  Nat Commun       Date:  2018-03-09       Impact factor: 14.919

9.  Moesin is involved in polarity maintenance and cortical remodeling during asymmetric cell division.

Authors:  Namal Abeysundara; Andrew J Simmonds; Sarah C Hughes
Journal:  Mol Biol Cell       Date:  2017-12-27       Impact factor: 4.138

  9 in total

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