Literature DB >> 26813976

Gradient COUP-TFI Expression Is Required for Functional Organization of the Hippocampal Septo-Temporal Longitudinal Axis.

Gemma Flore1,2, Giuseppina Di Ruberto2, Joséphine Parisot3,4, Sara Sannino1, Fabio Russo1, Elizabeth A Illingworth1,2, Michèle Studer1,3,4, Elvira De Leonibus1,2.   

Abstract

The hippocampus (HP), a medial cortical structure, is subdivided into a distinct dorsal (septal) and ventral (temporal) portion, which is separated by an intermediate region lying on a longitudinal curvature. While the dorsal portion is more dedicated to spatial navigation and memory, the most ventral part processes emotional information. Genetic factors expressed in gradient during development seem to control the size and correct positioning of the HP along its longitudinal axis; however, their roles in regulating differential growth and in supporting its anatomical and functional dissociation remain unexplored. Here, we challenge the in vivo function of the nuclear receptor COUP-TFI (chicken ovalbumin upstream promoter transcription factor 1) in controlling the hippocampal, anatomical, and functional properties along its longitudinal axis. Loss of cortical COUP-TFI function results in a dysmorphic HP with altered shape, volume, and connectivity, particularly in its dorsal and intermediate regions. Notably, topographic inputs from the entorhinal cortex are strongly impaired in the dorsal portion of COUP-TFI mutants. These severe morphological changes are associated with selective spatial learning and memory impairment. These findings identify a novel transcriptional regulator required in the functional organization along the hippocampal septo-temporal axis supporting a genetic basis of the hippocampal volumetric growth with its final shape, circuit, and type of memory function.
© The Author 2016. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  COUP-TFI gradient expression; entorhinal connectivity; hippocampus; septo-temporal longitudinal axis; spatial memory

Mesh:

Substances:

Year:  2017        PMID: 26813976     DOI: 10.1093/cercor/bhv336

Source DB:  PubMed          Journal:  Cereb Cortex        ISSN: 1047-3211            Impact factor:   5.357


  11 in total

1.  Nr2f1 heterozygous knockout mice recapitulate neurological phenotypes of Bosch-Boonstra-Schaaf optic atrophy syndrome and show impaired hippocampal synaptic plasticity.

Authors:  Chun-An Chen; Wei Wang; Steen E Pedersen; Ayush Raman; Michelle L Seymour; Fernanda R Ruiz; Anping Xia; Meike E van der Heijden; Li Wang; Jiani Yin; Joanna Lopez; Megan E Rech; Richard A Lewis; Samuel M Wu; Zhandong Liu; Fred A Pereira; Robia G Pautler; Huda Y Zoghbi; Christian P Schaaf
Journal:  Hum Mol Genet       Date:  2020-03-27       Impact factor: 6.150

2.  Dynamic expression of NR2F1 and SOX2 in developing and adult human cortex: comparison with cortical malformations.

Authors:  Benedetta Foglio; Laura Rossini; Rita Garbelli; Maria Cristina Regondi; Sara Mercurio; Michele Bertacchi; Laura Avagliano; Gaetano Bulfamante; Roland Coras; Antonino Maiorana; Silvia Nicolis; Michèle Studer; Carolina Frassoni
Journal:  Brain Struct Funct       Date:  2021-03-04       Impact factor: 3.270

3.  Mouse Nr2f1 haploinsufficiency unveils new pathological mechanisms of a human optic atrophy syndrome.

Authors:  Michele Bertacchi; Agnès Gruart; Polynikis Kaimakis; Cécile Allet; Linda Serra; Paolo Giacobini; José M Delgado-García; Paola Bovolenta; Michèle Studer
Journal:  EMBO Mol Med       Date:  2019-07-18       Impact factor: 12.137

Review 4.  Structural and Functional Aspects of the Neurodevelopmental Gene NR2F1: From Animal Models to Human Pathology.

Authors:  Chiara Tocco; Michele Bertacchi; Michèle Studer
Journal:  Front Mol Neurosci       Date:  2021-12-15       Impact factor: 5.639

5.  The topography of corticopontine projections is controlled by postmitotic expression of the area-mapping gene Nr2f1.

Authors:  Chiara Tocco; Martin Øvsthus; Jan G Bjaalie; Trygve B Leergaard; Michèle Studer
Journal:  Development       Date:  2022-03-09       Impact factor: 6.868

6.  Mitochondrial involvement in a Bosch-Boonstra-Schaaf optic atrophy syndrome patient with a novel de novo NR2F1 gene mutation.

Authors:  Elena Martín-Hernández; María Elena Rodríguez-García; Chun-An Chen; Francisco Javier Cotrina-Vinagre; Patricia Carnicero-Rodríguez; Marcello Bellusci; Christian P Schaaf; Francisco Martínez-Azorín
Journal:  J Hum Genet       Date:  2018-02-06       Impact factor: 3.172

7.  The Transcription Factors COUP-TFI and COUP-TFII have Distinct Roles in Arealisation and GABAergic Interneuron Specification in the Early Human Fetal Telencephalon.

Authors:  Ayman Alzu'bi; Susan J Lindsay; Lauren F Harkin; Jack McIntyre; Steven N Lisgo; Gavin J Clowry
Journal:  Cereb Cortex       Date:  2017-10-01       Impact factor: 5.357

8.  NR2F1 regulates regional progenitor dynamics in the mouse neocortex and cortical gyrification in BBSOAS patients.

Authors:  Michele Bertacchi; Anna Lisa Romano; Agnès Loubat; Frederic Tran Mau-Them; Marjolaine Willems; Laurence Faivre; Philippe Khau van Kien; Laurence Perrin; Françoise Devillard; Arthur Sorlin; Paul Kuentz; Christophe Philippe; Aurore Garde; Francesco Neri; Rossella Di Giaimo; Salvatore Oliviero; Silvia Cappello; Ludovico D'Incerti; Carolina Frassoni; Michèle Studer
Journal:  EMBO J       Date:  2020-06-02       Impact factor: 11.598

Review 9.  New insights into the development of the human cerebral cortex.

Authors:  Zoltán Molnár; Gavin J Clowry; Nenad Šestan; Ayman Alzu'bi; Trygve Bakken; Robert F Hevner; Petra S Hüppi; Ivica Kostović; Pasko Rakic; E S Anton; David Edwards; Patricia Garcez; Anna Hoerder-Suabedissen; Arnold Kriegstein
Journal:  J Anat       Date:  2019-08-02       Impact factor: 2.610

Review 10.  Novel Perspectives on the Development of the Amygdala in Rodents.

Authors:  Tania Aerts; Eve Seuntjens
Journal:  Front Neuroanat       Date:  2021-12-09       Impact factor: 3.856

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