DLX genes and proteins in mammalian forebrain development

Author:

Rubenstein John L.1ORCID,Nord Alex S.2ORCID,Ekker Marc3

Affiliation:

1. University of California San Francisco 1 UCSF Department of Psychiatry and Behavioral Sciences, Department of UCSF Weill Institute for Neurosciences, Nina Ireland Laboratory of Developmental Neurobiology , , San Francisco, CA 94143 , USA

2. Center for Neuroscience, University of California Davis 2 Department of Neurobiology, Physiology, and Behavior and Department of Psychiatry and 20 Behavioral Sciences , , Davis, CA 95618 , USA

3. University of Ottawa 3 Department of Biology , , 30 Marie Curie, Ottawa, ON K1N 6N5 , Canada

Abstract

ABSTRACT The vertebrate Dlx gene family encode homeobox transcription factors that are related to the Drosophila Distal-less (Dll) gene and are crucial for development. Over the last ∼35 years detailed information has accrued about the redundant and unique expression and function of the six mammalian Dlx family genes. DLX proteins interact with general transcriptional regulators, and co-bind with other transcription factors to enhancer elements with highly specific activity in the developing forebrain. Integration of the genetic and biochemical data has yielded a foundation for a gene regulatory network governing the differentiation of forebrain GABAergic neurons. In this Primer, we describe the discovery of vertebrate Dlx genes and their crucial roles in embryonic development. We largely focus on the role of Dlx family genes in mammalian forebrain development revealed through studies in mice. Finally, we highlight questions that remain unanswered regarding vertebrate Dlx genes despite over 30 years of research.

Funder

National Institute of Mental Health

Natural Sciences and Engineering Research Council of Canada

National Institute of General Medical Sciences

Publisher

The Company of Biologists

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