Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (39)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Sheen, V. L.
Right arrow Articles by Walsh, C. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sheen, V. L.
Right arrow Articles by Walsh, C. A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Molecular Genetics, 2002, Vol. 11, No. 23 2845-2854
© 2002 Oxford University Press

Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact

Volney L. Sheen1,{dagger}, Yuanyi Feng1,{dagger}, Donna Graham1, Toshiro Takafuta2, Sandor S. Shapiro2 and Christopher A. Walsh1,3,*

1Division of Neurogenetics, Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Institutes of Medicine, Boston, Massachusetts 02115, USA, 2Cardeza Foundation for Hematologic Research, Department of Medicine, Jefferson Medical College, Philadelphia, Pennsylvania 19107, USA and 3Program in Biological and Biomedical Sciences, Harvard Medical School, Boston, Massachusetts 02115, USA

Received June 21, 2002; Revised August 17, 2002; Accepted August 26, 2002

Mutations in the X-linked gene Filamin A (FLNA) lead to the human neurological disorder, periventricular heterotopia (PH). Although PH is characterized by a failure in neuronal migration into the cerebral cortex with consequent formation of nodules in the ventricular and subventricular zones, many neurons appear to migrate normally, even in males, suggesting compensatory mechanisms. Here we characterize expression patterns for FlnA and a highly homologous protein Filamin B (FlnB) within the nervous system, in order to better understand their potential roles in cortical development. FlnA mRNA was widely expressed in all cortical layers while FlnB mRNA was most highly expressed in the ventricular and subventricular zones during development. In adulthood, widespread but reduced expression of FlnA and FlnB persisted throughout the cerebral cortex. FlnA and FlnB proteins were highly expressed in both the leading processes and somata of migratory neurons during corticogenesis. Postnatally, FlnA immunoreactivity was largely localized to the cell body with FlnB in the soma and neuropil during neuronal differentiation. In adulthood, diminished expression of both proteins localized to the cell soma and nucleus. Moreover, the putative FLNB homodimerization domain strongly interacted with itself or the corresponding homologous region of FLNA by yeast two-hybrid interaction, the two proteins co-localized within neuronal precursors by immunocytochemistry and the existence of FLNA–FLNB heterodimers could be detected by co-immunoprecipitation. These results suggest that FLNA and FLNB may form both homodimers and heterodimers and that their interaction could potentially compensate for the loss of FLNA function during cortical development within PH individuals.

* To whom correspondence should be addressed at: Room 816, Harvard Institutes of Medicine, 77 Avenue Louis Pasteur, Boston, MA, USA. Tel: +1 6176670813; Fax: +1 6176670815; Email: cwalsh{at}caregroup.harvard.edu

{dagger} The authors wish it to be known, that in their opinion, the first two authors should be regarded as joint First Authors.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Hum Mol GenetHome page
R. J. Ferland, L. F. Batiz, J. Neal, G. Lian, E. Bundock, J. Lu, Y.-C. Hsiao, R. Diamond, D. Mei, A. H. Banham, et al.
Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia
Hum. Mol. Genet., February 1, 2009; 18(3): 497 - 516.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
J. Lu, G. Lian, R. Lenkinski, A. De Grand, R. R. Vaid, T. Bryce, M. Stasenko, A. Boskey, C. Walsh, and V. Sheen
Filamin B mutations cause chondrocyte defects in skeletal development
Hum. Mol. Genet., July 15, 2007; 16(14): 1661 - 1675.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
X. Zhou, F. Tian, J. Sandzen, R. Cao, E. Flaberg, L. Szekely, Y. Cao, C. Ohlsson, M. O. Bergo, J. Boren, et al.
Filamin B deficiency in mice results in skeletal malformations and impaired microvascular development
PNAS, March 6, 2007; 104(10): 3919 - 3924.
[Abstract] [Full Text] [PDF]


Home page
J. Med. Genet.Home page
L. S Bicknell, C. Farrington-Rock, Y. Shafeghati, P. Rump, Y. Alanay, Y. Alembik, N. Al-Madani, H. Firth, M. H. Karimi-Nejad, C. A. Kim, et al.
A molecular and clinical study of Larsen syndrome caused by mutations in FLNB
J. Med. Genet., February 1, 2007; 44(2): 89 - 98.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
Y. Feng, M. H. Chen, I. P. Moskowitz, A. M. Mendonza, L. Vidali, F. Nakamura, D. J. Kwiatkowski, and C. A. Walsh
Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis
PNAS, December 26, 2006; 103(52): 19836 - 19841.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
A. W. Hart, J. E. Morgan, J. Schneider, K. West, L. McKie, S. Bhattacharya, I. J. Jackson, and S. H. Cross
Cardiac malformations and midline skeletal defects in mice lacking filamin A
Hum. Mol. Genet., August 15, 2006; 15(16): 2457 - 2467.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
E. Parrini, A. Ramazzotti, W. B. Dobyns, D. Mei, F. Moro, P. Veggiotti, C. Marini, E. H. Brilstra, B. D. Bernardina, L. Goodwin, et al.
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations
Brain, July 1, 2006; 129(7): 1892 - 1906.
[Abstract] [Full Text] [PDF]


Home page
J. Med. Genet.Home page
U Hehr, A Hehr, G Uyanik, E Phelan, J Winkler, and W Reardon
A filamin A splice mutation resulting in a syndrome of facial dysmorphism, periventricular nodular heterotopia, and severe constipation reminiscent of cerebro-fronto-facial syndrome
J. Med. Genet., June 1, 2006; 43(6): 541 - 544.
[Abstract] [Full Text] [PDF]


Home page
J. Med. Genet.Home page
P Gomez-Garre, M Seijo, E Gutierrez-Delicado, M Castro del Rio, C de la Torre, C Gomez-Abad, J Morales-Corraliza, M Puig, and J M Serratosa
Ehlers-Danlos syndrome and periventricular nodular heterotopia in a Spanish family with a single FLNA mutation
J. Med. Genet., March 1, 2006; 43(3): 232 - 237.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
T. Nagano, S. Morikubo, and M. Sato
Filamin A and FILIP (Filamin A-Interacting Protein) Regulate Cell Polarity and Motility in Neocortical Subventricular and Intermediate Zones during Radial Migration
J. Neurosci., October 27, 2004; 24(43): 9648 - 9657.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
R. Guerrini, D. Mei, S. Sisodiya, F. Sicca, B. Harding, Y. Takahashi, T. Dorn, A. Yoshida, J. Campistol, G. Kramer, et al.
Germline and mosaic mutations of FLN1 in men with periventricular heterotopia
Neurology, July 13, 2004; 63(1): 51 - 56.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
M. S. Woo, Y. Ohta, I. Rabinovitz, T. P. Stossel, and J. Blenis
Ribosomal S6 Kinase (RSK) Regulates Phosphorylation of Filamin A on an Important Regulatory Site
Mol. Cell. Biol., April 1, 2004; 24(7): 3025 - 3035.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
V. L. Sheen, M. Topcu, S. Berkovic, D. Yalnizoglu, I. Blatt, A. Bodell, R. S. Hill, V. S. Ganesh, T. J. Cherry, Y. Y. Shugart, et al.
Autosomal recessive form of periventricular heterotopia
Neurology, April 8, 2003; 60(7): 1108 - 1112.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.