Literature DB >> 21893162

The expression and localization of Prune2 mRNA in the central nervous system.

Shimo Li1, Masanori Itoh, Kazunori Ohta, Masashi Ueda, Akihito Mizuno, Eri Ohta, Yoko Hida, Miao-Xing Wang, Kazunori Takeuchi, Toshiyuki Nakagawa.   

Abstract

A family of Bcl-2/adenovirus E1B 19kDa-interacting proteins (BNIPs) plays critical roles in several cellular processes such as cellular transformation, apoptosis, neuronal differentiation, and synaptic function, which are mediated by the BNIP2 and Cdc42GAP homology (BCH) domain. Prune homolog 2 (Drosophila) (PRUNE2) and its isoforms -C9orf65, BCH motif-containing molecule at the carboxyl terminal region 1 (BMCC1), and BNIP2 Extra Long (BNIPXL) - have been shown to be a susceptibility gene for Alzheimer's disease, a biomarker for leiomyosarcomas, a proapoptotic protein in neuronal cells, and an antagonist of cellular transformation, respectively. However, precise localization of PRUNE2 in the brain remains unclear. Here, we identified the distribution of Prune2 mRNA in the adult mouse brain. Prune2 mRNA is predominantly expressed in the neurons of the cranial nerve motor nuclei and the motor neurons of the spinal cord. The expression in the dorsal root ganglia (DRG) is consistent with the previously described reports. In addition, we observed the expression in another sensory neuron in the mesencephalic trigeminal nucleus. These results suggest that Prune2 may be functional in these restricted brain regions.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

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Year:  2011        PMID: 21893162     DOI: 10.1016/j.neulet.2011.08.037

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  4 in total

1.  Prune homolog 2 with BCH domain (PRUNE2) gene expression is associated with feed efficiency-related traits in Nelore steers.

Authors:  Andressa Oliveira Lima; Jessica Moraes Malheiros; Juliana Afonso; Juliana Petrini; Luiz Lehmann Coutinho; Wellison Jarles da Silva Diniz; Flávia Aline Bressani; Polyana Cristine Tizioto; Priscila Silva Neubern de Oliveira; Janssen Ayna Silva Ribeiro; Karina Santos de Oliveira; Marina Ibelli Pereira Rocha; Bruno Gabriel Nascimento Andrade; Heidge Fukumasu; Hamid Beiki; James Mark Reecy; Adhemar Zerlotini; Gerson Barreto Mourao; Luciana Correia de Almeida Regitano
Journal:  Mamm Genome       Date:  2022-07-16       Impact factor: 3.224

2.  A smooth muscle-like origin for beige adipocytes.

Authors:  Jonathan Z Long; Katrin J Svensson; Linus Tsai; Xing Zeng; Hyun C Roh; Xingxing Kong; Rajesh R Rao; Jesse Lou; Isha Lokurkar; Wendy Baur; John J Castellot; Evan D Rosen; Bruce M Spiegelman
Journal:  Cell Metab       Date:  2014-04-04       Impact factor: 27.287

3.  Bmcc1s, a novel brain-isoform of Bmcc1, affects cell morphology by regulating MAP6/STOP functions.

Authors:  Jessica Arama; Anne-Cécile Boulay; Christophe Bosc; Christian Delphin; Damarys Loew; Philippe Rostaing; Edwige Amigou; Pascal Ezan; Laure Wingertsmann; Laurent Guillaud; Annie Andrieux; Christian Giaume; Martine Cohen-Salmon
Journal:  PLoS One       Date:  2012-04-16       Impact factor: 3.240

4.  BMCC1 is an AP-2 associated endosomal protein in prostate cancer cells.

Authors:  Janelle L Harris; Renée S Richards; Clement W K Chow; Soon Lee; Misook Kim; Marion Buck; Linda Teng; Raymond Clarke; Robert A Gardiner; Martin F Lavin
Journal:  PLoS One       Date:  2013-09-06       Impact factor: 3.240

  4 in total

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