Literature DB >> 10498683

Lis1, the Drosophila homolog of a human lissencephaly disease gene, is required for germline cell division and oocyte differentiation.

Z Liu1, T Xie, R Steward.   

Abstract

Lissencephaly is a severe congenital brain malformation resulting from incomplete neuronal migration. One causal gene, LIS1, is homologous to nudF, a gene required for nuclear migration in A. nidulans. We have characterized the Drosophila homolog of LIS1 (Lis1) and show that Lis1 is essential for fly development. Analysis of ovarian Lis1 mutant clones demonstrates that Lis1 is required in the germline for synchronized germline cell division, fusome integrity and oocyte differentiation. Abnormal packaging of the cysts was observed in Lis1 mutant clones. Our results indicate that LIS1 is important for cell division and differentiation and the function of the membrane cytoskeleton. They support the notion that LIS1 functions with the dynein complex to regulate nuclear migration or cell migration.

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Year:  1999        PMID: 10498683     DOI: 10.1242/dev.126.20.4477

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  41 in total

1.  LIS1, CLIP-170's key to the dynein/dynactin pathway.

Authors:  Frédéric M Coquelle; Michal Caspi; Fabrice P Cordelières; Jim P Dompierre; Denis L Dujardin; Cynthia Koifman; Patrick Martin; Casper C Hoogenraad; Anna Akhmanova; Niels Galjart; Jan R De Mey; Orly Reiner
Journal:  Mol Cell Biol       Date:  2002-05       Impact factor: 4.272

Review 2.  Miller-Dieker syndrome: analysis of a human contiguous gene syndrome in the mouse.

Authors:  Jessica Yingling; Kazuhito Toyo-Oka; Anthony Wynshaw-Boris
Journal:  Am J Hum Genet       Date:  2003-08-05       Impact factor: 11.025

3.  Live imaging of Drosophila brain neuroblasts reveals a role for Lis1/dynactin in spindle assembly and mitotic checkpoint control.

Authors:  Karsten H Siller; Madeline Serr; Ruth Steward; Tom S Hays; Chris Q Doe
Journal:  Mol Biol Cell       Date:  2005-08-17       Impact factor: 4.138

4.  Lissencephaly-1 controls germline stem cell self-renewal through modulating bone morphogenetic protein signaling and niche adhesion.

Authors:  Shuyi Chen; Satoshi Kaneko; Xing Ma; Xiaochu Chen; Y Tony Ip; Lan Xu; Ting Xie
Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-01       Impact factor: 11.205

Review 5.  Cease and desist: modulating short-range Dpp signalling in the stem-cell niche.

Authors:  Robin E Harris; Hilary L Ashe
Journal:  EMBO Rep       Date:  2011-05-06       Impact factor: 8.807

Review 6.  Mechanism and regulation of cytoplasmic dynein.

Authors:  Michael A Cianfrocco; Morgan E DeSantis; Andres E Leschziner; Samara L Reck-Peterson
Journal:  Annu Rev Cell Dev Biol       Date:  2015-09-30       Impact factor: 13.827

7.  Progression from mitotic catastrophe to germ cell death in Caenorhabditis elegans lis-1 mutants requires the spindle checkpoint.

Authors:  Edgar A Buttner; Aleksandra J Gil-Krzewska; Anandita K Rajpurohit; Craig P Hunter
Journal:  Dev Biol       Date:  2007-02-24       Impact factor: 3.582

8.  Complete loss of Ndel1 results in neuronal migration defects and early embryonic lethality.

Authors:  Shinji Sasaki; Daisuke Mori; Kazuhito Toyo-oka; Amy Chen; Lisa Garrett-Beal; Masami Muramatsu; Shuji Miyagawa; Noriko Hiraiwa; Atsushi Yoshiki; Anthony Wynshaw-Boris; Shinji Hirotsune
Journal:  Mol Cell Biol       Date:  2005-09       Impact factor: 4.272

9.  Rab-mediated vesicular transport is required for neuronal positioning in the developing Drosophila visual system.

Authors:  Tarek Houalla; Lei Shi; Donald J van Meyel; Yong Rao
Journal:  Mol Brain       Date:  2010-06-11       Impact factor: 4.041

10.  Regulators of the actin cytoskeleton mediate lethality in a Caenorhabditis elegans dhc-1 mutant.

Authors:  Aleksandra J Gil-Krzewska; Erica Farber; Edgar A Buttner; Craig P Hunter
Journal:  Mol Biol Cell       Date:  2010-06-16       Impact factor: 4.138

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