Knockdown of Dyslexia-GeneDcdc2Interferes with Speech Sound Discrimination in Continuous Streams
| Autor: | Joseph J. LoTurco, Anne B. Booker, Ryan S. Carraway, Michael P. Kilgard, Fuyi Chen, Tracy M. Centanni, Robert L. Rennaker, Andrew M. Sloan |
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| Přispěvatelé: | McGovern Institute for Brain Research at MIT, Centanni, Tracy M |
| Rok vydání: | 2016 |
| Předmět: |
Male
0301 basic medicine medicine.medical_specialty Speech perception education Audiology Dyslexia 03 medical and health sciences 0302 clinical medicine DCDC2 otorhinolaryngologic diseases medicine Animals health care economics and organizations Auditory Cortex Gene knockdown Neuronal Plasticity Speech sound General Neuroscience Articles medicine.disease Rats Sound 030104 developmental biology Acoustic Stimulation Auditory Perception Speech Perception Female RNA Interference Psychology Microtubule-Associated Proteins 030217 neurology & neurosurgery |
| Zdroj: | Society for Neuroscience |
| ISSN: | 1529-2401 0270-6474 |
| DOI: | 10.1523/jneurosci.4202-15.2016 |
| Popis: | Dyslexia is the most common developmental language disorder and is marked by deficits in reading and phonological awareness. One theory of dyslexia suggests that the phonological awareness deficit is due to abnormal auditory processing of speech sounds. Variants in DCDC2 and several other neural migration genes are associated with dyslexia and may contribute to auditory processing deficits. In the current study, wetestedthe hypothesisthat RNAi suppression of Dcdc2 in rats causes abnormal cortical responsesto sound and impaired speech sound discrimination. In the current study, rats were subjected in utero to RNA interference targeting of the gene Dcdc2 or a scrambled sequence. Primary auditory cortex (A1) responseswere acquiredfrom 11 rats (5withDcdc2RNAi; DC) before any behavioral training. A separate group of 8 rats (3 DC)weretrained on a variety of speech sound discriminationtasks, and auditory cortex responses were acquired following training. Dcdc2 RNAi nearly eliminated the ability of rats to identify specific speech sounds from a continuous train of speech sounds but did not impair performance during discrimination of isolated speech sounds. The neural responses to speech sounds in A1 were not degraded as a function of presentation rate before training. These results suggest that A1 is not directly involved in the impaired speech discrimination caused by Dcdc2 RNAi. This result contrasts earlier results using Kiaa0319 RNAi and suggests that different dyslexia genes may cause different deficits in the speech processing circuitry, which may explain differential responses to therapy. National Institute on Deafness and Other Communication Disorders (U.S.) (Grant R01DC010433) |
| Databáze: | OpenAIRE |
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