Literature DB >> 1627461

The reeler gene: a clue to brain development and evolution.

A M Goffinet1.   

Abstract

Reeler mutant mice are characterized by profuse anomalies of cell positioning in the telencephalic and cerebellar cortices as well as by distinct malformations in non-cortical structures such as the inferior olive, the facial nerve nucleus and other brainstem nuclei. Studies of the embryonic development of these structures reveal that the early cell patterns formed by reeler neurons is consistently affected, so that the reeler gene plays an important role in the development of nerve cell patterns. Comparative studies of cortical development in reptiles suggest further that the mammalian type of cortical architectonics has been acquired progressively during brain evolution, and reveal some similarities in early cortical organization between reeler and reptilian, particularly chelonian, embryos, most notably the presence of an inverted gradient of cortical histogenesis. These observations point to a possible role of the reeler gene in cortical evolution. Although the factors responsible for the formation of neural cell patterns are largely unknown, most data point to the importance of cell-cell interactions. Cell-interaction molecules have probably been acquired during brain evolution and the reeler gene could act by perturbing, directly or indirectly, such cell interactions. The characterization and thus the cloning of the reeler gene is therefore important for our understanding of brain development. Recent data on the fine chromosomal mapping of the mutation prior to its positional cloning are reported.

Entities:  

Mesh:

Year:  1992        PMID: 1627461

Source DB:  PubMed          Journal:  Int J Dev Biol        ISSN: 0214-6282            Impact factor:   2.203


  8 in total

Review 1.  Thyroid hormone and cerebellar development.

Authors:  Grant W Anderson
Journal:  Cerebellum       Date:  2008       Impact factor: 3.847

2.  Thyroid hormone regulates reelin and dab1 expression during brain development.

Authors:  M Alvarez-Dolado; M Ruiz; J A Del Río; S Alcántara; F Burgaya; M Sheldon; K Nakajima; J Bernal; B W Howell; T Curran; E Soriano; A Muñoz
Journal:  J Neurosci       Date:  1999-08-15       Impact factor: 6.167

3.  Association analysis of two single-nucleotide polymorphisms of the RELN gene with autism in the South African population.

Authors:  Jyoti Rajan Sharma; Zainunisha Arieff; Hajirah Gameeldien; Muneera Davids; Mandeep Kaur; Lize van der Merwe
Journal:  Genet Test Mol Biomarkers       Date:  2012-12-05

4.  Birthdate and cell marker analysis of scrambler: a novel mutation affecting cortical development with a reeler-like phenotype.

Authors:  J L González; C J Russo; D Goldowitz; H O Sweet; M T Davisson; C A Walsh
Journal:  J Neurosci       Date:  1997-12-01       Impact factor: 6.167

5.  Isolation of an allele of reeler by insertional mutagenesis.

Authors:  G G Miao; R J Smeyne; G D'Arcangelo; N G Copeland; N A Jenkins; J I Morgan; T Curran
Journal:  Proc Natl Acad Sci U S A       Date:  1994-11-08       Impact factor: 11.205

6.  Regional and cellular patterns of reelin mRNA expression in the forebrain of the developing and adult mouse.

Authors:  S Alcántara; M Ruiz; G D'Arcangelo; F Ezan; L de Lecea; T Curran; C Sotelo; E Soriano
Journal:  J Neurosci       Date:  1998-10-01       Impact factor: 6.167

7.  Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.

Authors:  Emanuela Dazzo; Manuela Fanciulli; Elena Serioli; Giovanni Minervini; Patrizia Pulitano; Simona Binelli; Carlo Di Bonaventura; Concetta Luisi; Elena Pasini; Salvatore Striano; Pasquale Striano; Giangennaro Coppola; Angela Chiavegato; Slobodanka Radovic; Alessandro Spadotto; Sergio Uzzau; Angela La Neve; Anna Teresa Giallonardo; Oriano Mecarelli; Silvio C E Tosatto; Ruth Ottman; Roberto Michelucci; Carlo Nobile
Journal:  Am J Hum Genet       Date:  2015-06-04       Impact factor: 11.025

8.  Comparative analysis of squamate brains unveils multi-level variation in cerebellar architecture associated with locomotor specialization.

Authors:  Simone Macrì; Yoland Savriama; Imran Khan; Nicolas Di-Poï
Journal:  Nat Commun       Date:  2019-12-05       Impact factor: 14.919

  8 in total

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