Literature DB >> 10349626

Mab21, the mouse homolog of a C. elegans cell-fate specification gene, participates in cerebellar, midbrain and eye development.

M Mariani1, A Corradi, D Baldessari, N Malgaretti, O Pozzoli, R Fesce, S Martinez, E Boncinelli, G G Consalez.   

Abstract

A multitude of regulatory genes are involved in phylogenetically conserved developmental cascades required for the patterning, cell-type specification, and differentiation of specific central nervous system (CNS) structures. Here, we describe the distribution of a mouse transcript encoding a homolog of the C. elegans mab-21 gene. In the nematode tail, mab-21 is required for the short-range patterning and cell-fate determination events mediated by egl-5 and mab-18, two homeobox genes homologous to Abd-B and Pax6, respectively. In mouse midgestation embryogenesis, Mab21 is expressed at its highest levels in the rhombencephalon, cerebellum, midbrain, and prospective neural retina. Our data and the genetic interactions previously documented in the nematode suggest that Mab21 may represent a novel, important regulator of mammalian cerebellum and eye development.

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Year:  1998        PMID: 10349626     DOI: 10.1016/s0925-4773(98)00180-4

Source DB:  PubMed          Journal:  Mech Dev        ISSN: 0925-4773            Impact factor:   1.882


  12 in total

1.  DNA microarray analysis of functionally discrete human brain regions reveals divergent transcriptional profiles.

Authors:  S J Evans; P V Choudary; M P Vawter; J Li; J H Meador-Woodruff; J F Lopez; S M Burke; R C Thompson; R M Myers; E G Jones; W E Bunney; S J Watson; H Akil
Journal:  Neurobiol Dis       Date:  2003-11       Impact factor: 5.996

2.  Analysis of the eye developmental pathway in Drosophila using DNA microarrays.

Authors:  Lydia Michaut; Susanne Flister; Martin Neeb; Kevin P White; Ulrich Certa; Walter J Gehring
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-24       Impact factor: 11.205

3.  Doublesex and mab-3-related transcription factor 5 promotes midbrain dopaminergic identity in pluripotent stem cells by enforcing a ventral-medial progenitor fate.

Authors:  Nicole Gennet; Emily Gale; Xinsheng Nan; Emma Farley; Katalin Takacs; Barbara Oberwallner; David Chambers; Meng Li
Journal:  Proc Natl Acad Sci U S A       Date:  2011-05-16       Impact factor: 11.205

4.  Xmab21l3 mediates dorsoventral patterning in Xenopus laevis.

Authors:  Jyotsna Sridharan; Tomomi Haremaki; Ye Jin; Sushma Teegala; Daniel C Weinstein
Journal:  Mech Dev       Date:  2012-05-15       Impact factor: 1.882

5.  Monoallelic and biallelic mutations in MAB21L2 cause a spectrum of major eye malformations.

Authors:  Joe Rainger; Davut Pehlivan; Stefan Johansson; Hemant Bengani; Luis Sanchez-Pulido; Kathleen A Williamson; Mehmet Ture; Heather Barker; Karen Rosendahl; Jürgen Spranger; Denise Horn; Alison Meynert; James A B Floyd; Trine Prescott; Carl A Anderson; Jacqueline K Rainger; Ender Karaca; Claudia Gonzaga-Jauregui; Shalini Jhangiani; Donna M Muzny; Anne Seawright; Dinesh C Soares; Mira Kharbanda; Victoria Murday; Andrew Finch; Richard A Gibbs; Veronica van Heyningen; Martin S Taylor; Tahsin Yakut; Per M Knappskog; Matthew E Hurles; Chris P Ponting; James R Lupski; Gunnar Houge; David R FitzPatrick
Journal:  Am J Hum Genet       Date:  2014-06-05       Impact factor: 11.025

6.  Mab21l2 is essential for embryonic heart and liver development.

Authors:  Yohei Saito; Takuya Kojima; Naoki Takahashi
Journal:  PLoS One       Date:  2012-03-08       Impact factor: 3.240

7.  MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1.

Authors:  Danila Baldessari; Aurora Badaloni; Renato Longhi; Vincenzo Zappavigna; G Giacomo Consalez
Journal:  BMC Cell Biol       Date:  2004-12-21       Impact factor: 4.241

8.  Structural and biochemical characterization of the cell fate determining nucleotidyltransferase fold protein MAB21L1.

Authors:  Carina C de Oliveira Mann; Reiner Kiefersauer; Gregor Witte; Karl-Peter Hopfner
Journal:  Sci Rep       Date:  2016-06-08       Impact factor: 4.379

9.  Differential expression of Meis2, Mab21l2 and Tbx3 during limb development associated with diversification of limb morphology in mammals.

Authors:  Mengyao Dai; Yao Wang; Lu Fang; David M Irwin; Tengteng Zhu; Junpeng Zhang; Shuyi Zhang; Zhe Wang
Journal:  PLoS One       Date:  2014-08-28       Impact factor: 3.240

10.  MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome).

Authors:  Abolfazl Rad; Umut Altunoglu; Rebecca Miller; Reza Maroofian; Natalie Hauser; Murat Gunel; Hulya Kayserili; Miriam Schmidts; Kiely N James; Ahmet Okay Çağlayan; Maryam Najafi; Valentina Stanley; Rose-Mary Boustany; Gözde Yeşil; Afsaneh Sahebzamani; Gülhan Ercan-Sencicek; Kolsoum Saeidi; Kaman Wu; Peter Bauer; Zeineb Bakey; Joseph G Gleeson
Journal:  J Med Genet       Date:  2018-11-28       Impact factor: 6.318

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