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<it>Kalrn </it>promoter usage and isoform expression respond to chronic cocaine exposure

By Ma Xin-Ming, Eipper-Mains Jodi E, Kiraly Drew D, Mains Richard E and Eipper Betty A

Abstract

<p>Abstract</p> <p>Background</p> <p>The long-term effects of cocaine on behavior are accompanied by structural changes in excitatory glutamatergic synapses onto the medium spiny neurons of the striatum. The <it>Kalrn </it>gene encodes several functionally distinct isoforms; these multidomain guanine nucleotide exchange factors (GEFs) contain additional domains known to interact with phosphatidylinositides as well as with a number of different proteins. Through their activation of Rho proteins and their interactions with other proteins, the different Kalirin isoforms affect cytoskeletal organization. Chronic exposure of adult male rodents to cocaine increases levels of Kalirin 7 in the striatum. When exposed chronically to cocaine, mice lacking Kalirin 7, the major adult isoform, fail to show an increase in dendritic spine density in the nucleus accumbens, show diminished place preference for cocaine, and exhibit increased locomotor activity in response to cocaine.</p> <p>Results</p> <p>The use of alternate promoters and 3'-terminal exons of the mouse <it>Kalrn </it>gene were investigated using real-time quantitative polymerase chain reaction. While the two most distal full-length <it>Kalrn </it>promoters are used equally in the prefrontal cortex, the more proximal of these promoters accounts for most of the transcripts expressed in the nucleus accumbens. The 3'-terminal exon unique to the Kalirin 7 isoform accounts for a greater percentage of the <it>Kalrn </it>transcripts in prefrontal cortex than in nucleus accumbens. Western blot analyses confirmed these differences. Chronic cocaine treatment increases usage of the promoter encoding the Δ-Kalirin isoforms but does not alter full-length Kalirin promoter usage. Usage of the 3'-terminal exon unique to Kalirin 7 increases following chronic cocaine exposure.</p> <p>Conclusions</p> <p><it>Kalrn </it>promoter and 3'-terminal exon utilization are region-specific. In the nucleus accumbens, cocaine-mediated alterations in promoter usage and 3'-terminal exon usage favor expression of Kalirin 7 and Δ-Kalirin 7. The Δ-isoform, which lacks a Sec14p domain and four of the nine spectrin-like repeats found in full-length Kalirin isoforms, increases spine headsize without increasing dendritic spine numbers. Thus cocaine-mediated changes in alternative splicing of the <it>Kalrn </it>gene may contribute importantly to the behavioral, morphological and biochemical responses observed.</p

Topics: Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571, Internal medicine, RC31-1245, Medicine, R, DOAJ:Neurology, DOAJ:Medicine (General), DOAJ:Health Sciences, Neurophysiology and neuropsychology, QP351-495
Publisher: BioMed Central
Year: 2011
DOI identifier: 10.1186/1471-2202-12-20
OAI identifier: oai:doaj.org/article:068b9872c1bc4a2c8bad547d443d726f
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