Literature DB >> 32017903

The role of cell lineage in the development of neuronal circuitry and function.

Volker Hartenstein1, Jaison J Omoto2, Jennifer K Lovick2.   

Abstract

Complex nervous systems have a modular architecture, whereby reiterative groups of neurons ("modules") that share certain structural and functional properties are integrated into large neural circuits. Neurons develop from proliferating progenitor cells that, based on their location and time of appearance, are defined by certain genetic programs. Given that genes expressed by a given progenitor play a fundamental role in determining the properties of its lineage (i.e., the neurons descended from that progenitor), one efficient developmental strategy would be to have lineages give rise to the structural modules of the mature nervous system. It is clear that this strategy plays an important role in neural development of many invertebrate animals, notably insects, where the availability of genetic techniques has made it possible to analyze the precise relationship between neuronal origin and differentiation since several decades. Similar techniques, developed more recently in the vertebrate field, reveal that functional modules of the mammalian cerebral cortex are also likely products of developmentally defined lineages. We will review studies that relate cell lineage to circuitry and function from a comparative developmental perspective, aiming at enhancing our understanding of neural progenitors and their lineages, and translating findings acquired in different model systems into a common conceptual framework.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cell fate; Cell lineage; Circuitry; Drosophila; Mouse; Neural progenitor; Proliferation; Xenopus; Zebrafish

Mesh:

Year:  2020        PMID: 32017903      PMCID: PMC7394725          DOI: 10.1016/j.ydbio.2020.01.012

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.148


  206 in total

Review 1.  Microcolumns in the cerebral cortex.

Authors:  E G Jones
Journal:  Proc Natl Acad Sci U S A       Date:  2000-05-09       Impact factor: 11.205

2.  Glomerular maps without cellular redundancy at successive levels of the Drosophila larval olfactory circuit.

Authors:  Ariane Ramaekers; Edwige Magnenat; Elizabeth C Marin; Nanaë Gendre; Gregory S X E Jefferis; Liqun Luo; Reinhard F Stocker
Journal:  Curr Biol       Date:  2005-06-07       Impact factor: 10.834

3.  Chinmo and neuroblast temporal identity.

Authors:  Chris Q Doe
Journal:  Cell       Date:  2006-10-20       Impact factor: 41.582

4.  Notch regulates the generation of diverse cell types from the lateral lineage of Drosophila antennal lobe.

Authors:  Abhijit Das; Heinrich Reichert; Veronica Rodrigues
Journal:  J Neurogenet       Date:  2010-03       Impact factor: 1.250

5.  Role of Notch signaling in establishing the hemilineages of secondary neurons in Drosophila melanogaster.

Authors:  James W Truman; Wanda Moats; Janet Altman; Elizabeth C Marin; Darren W Williams
Journal:  Development       Date:  2010-01       Impact factor: 6.868

6.  Neural lineages of the Drosophila brain: a three-dimensional digital atlas of the pattern of lineage location and projection at the late larval stage.

Authors:  Wayne Pereanu; Volker Hartenstein
Journal:  J Neurosci       Date:  2006-05-17       Impact factor: 6.167

7.  Genetic control of dorsoventral patterning and neuroblast specification in the Drosophila Central Nervous System.

Authors:  Guoyan Zhao; Scott R Wheeler; James B Skeath
Journal:  Int J Dev Biol       Date:  2007       Impact factor: 2.203

Review 8.  Notch signaling in the mammalian central nervous system: insights from mouse mutants.

Authors:  Keejung Yoon; Nicholas Gaiano
Journal:  Nat Neurosci       Date:  2005-06       Impact factor: 24.884

9.  Five points on columns.

Authors:  Kathleen S Rockland
Journal:  Front Neuroanat       Date:  2010-06-09       Impact factor: 3.856

10.  A complete developmental sequence of a Drosophila neuronal lineage as revealed by twin-spot MARCM.

Authors:  Hung-Hsiang Yu; Chih-Fei Kao; Yisheng He; Peng Ding; Jui-Chun Kao; Tzumin Lee
Journal:  PLoS Biol       Date:  2010-08-24       Impact factor: 8.029

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  1 in total

1.  Exocyst-mediated membrane trafficking of the lissencephaly-associated ECM receptor dystroglycan is required for proper brain compartmentalization.

Authors:  Andriy S Yatsenko; Mariya M Kucherenko; Yuanbin Xie; Henning Urlaub; Halyna R Shcherbata
Journal:  Elife       Date:  2021-02-23       Impact factor: 8.140

  1 in total

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