Literature DB >> 30628007

Identification of Novel Binding Partners for Transcription Factor Emx2.

Jennifer A Groves1, Cody Gillman2, Cierra N DeLay1, Todd T Kroll3.   

Abstract

The mammalian homolog of Drosophila empty spiracles 2 (Emx2) is a homeobox transcription factor that plays central roles in early development of the inner ear, pelvic and shoulder girdles, cerebral cortex, and urogenital organs. The role for Emx2 is best understood within the context of the development of the neocortical region of the cortex, where Emx2 is expressed in a high posterior-medial to low anterior-lateral gradient that regulates the partitioning of the neocortex into different functional fields that perform discrete computational tasks. Despite several lines of evidence demonstrating an Emx2 concentration-dependent mechanism for establishing functional areas within the developing neocortex, little is known about how Emx2 physically carries out this role. Although several binding partners for Emx2 have been identified (including Sp8, eIF4E, and Pbx1), no screens have been used to identify potential protein binding partners for this protein. We utilized a yeast two-hybrid screen using a library constructed from embryonic mouse cDNA in an attempt to identify novel binding partners for Emx2. This initial screen isolated two potential Emx2-binding partner proteins, Cnot6l and QkI-7. These novel Emx2-binding proteins are involved in multiple levels of mRNA metabolism that including splicing, mRNA export, translation, and destruction, thus making them interesting targets for further study.

Entities:  

Keywords:  Arealization; Cnot6l; Development; Emx2; Quaking

Mesh:

Substances:

Year:  2019        PMID: 30628007     DOI: 10.1007/s10930-019-09810-1

Source DB:  PubMed          Journal:  Protein J        ISSN: 1572-3887            Impact factor:   2.371


  48 in total

1.  Emx2 promotes symmetric cell divisions and a multipotential fate in precursors from the cerebral cortex.

Authors:  N Heins; F Cremisi; P Malatesta; R M Gangemi; G Corte; J Price; G Goudreau; P Gruss; M Götz
Journal:  Mol Cell Neurosci       Date:  2001-11       Impact factor: 4.314

Review 2.  Sam68, the KH domain-containing superSTAR.

Authors:  Kiven E Lukong; Stéphane Richard
Journal:  Biochim Biophys Acta       Date:  2003-12-05

3.  Nuclear translocation controlled by alternatively spliced isoforms inactivates the QUAKING apoptotic inducer.

Authors:  J Pilotte; D Larocque; S Richard
Journal:  Genes Dev       Date:  2001-04-01       Impact factor: 11.361

4.  EMX2 regulates sizes and positioning of the primary sensory and motor areas in neocortex by direct specification of cortical progenitors.

Authors:  Tadashi Hamasaki; Axel Leingärtner; Thomas Ringstedt; Dennis D M O'Leary
Journal:  Neuron       Date:  2004-08-05       Impact factor: 17.173

Review 5.  Extra-cell cycle regulatory functions of cyclin-dependent kinases (CDK) and CDK inhibitor proteins contribute to brain development and neurological disorders.

Authors:  Takeshi Kawauchi; Mima Shikanai; Yoichi Kosodo
Journal:  Genes Cells       Date:  2013-01-07       Impact factor: 1.891

6.  Emx1 and Emx2 functions in development of dorsal telencephalon.

Authors:  M Yoshida; Y Suda; I Matsuo; N Miyamoto; N Takeda; S Kuratani; S Aizawa
Journal:  Development       Date:  1997-01       Impact factor: 6.868

7.  The STAR protein QKI-7 recruits PAPD4 to regulate post-transcriptional polyadenylation of target mRNAs.

Authors:  Ryota Yamagishi; Takeshi Tsusaka; Hiroko Mitsunaga; Takaharu Maehata; Shin-ichi Hoshino
Journal:  Nucleic Acids Res       Date:  2016-02-29       Impact factor: 16.971

8.  Regulation of Emx2 expression by antisense transcripts in murine cortico-cerebral precursors.

Authors:  Giulia Spigoni; Chiara Gedressi; Antonello Mallamaci
Journal:  PLoS One       Date:  2010-01-11       Impact factor: 3.240

9.  The QKI-6 and QKI-7 RNA binding proteins block proliferation and promote Schwann cell myelination.

Authors:  Daniel Larocque; Gabriela Fragoso; Jinghan Huang; Walter E Mushynski; Martin Loignon; Stéphane Richard; Guillermina Almazan
Journal:  PLoS One       Date:  2009-06-11       Impact factor: 3.240

10.  The CCR4 deadenylase acts with Nanos and Pumilio in the fine-tuning of Mei-P26 expression to promote germline stem cell self-renewal.

Authors:  Willy Joly; Aymeric Chartier; Patricia Rojas-Rios; Isabelle Busseau; Martine Simonelig
Journal:  Stem Cell Reports       Date:  2013-11-07       Impact factor: 7.765

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