Cargando…

Genetic analysis of posterior medial barrel subfield (PMBSF) size in somatosensory cortex (SI) in recombinant inbred strains of mice

BACKGROUND: Quantitative trait locus (QTL) mapping is an important tool for identifying potential candidate genes linked to complex traits. QTL mapping has been used to identify genes associated with cytoarchitecture, cell number, brain size, and brain volume. Previously, QTL mapping was utilized to...

Descripción completa

Detalles Bibliográficos
Autores principales: Jan, Taha A, Lu, Lu, Li, Cheng-Xiang, Williams, Robert W, Waters, Robert S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2254631/
https://www.ncbi.nlm.nih.gov/pubmed/18179704
http://dx.doi.org/10.1186/1471-2202-9-3
_version_ 1782151209799385088
author Jan, Taha A
Lu, Lu
Li, Cheng-Xiang
Williams, Robert W
Waters, Robert S
author_facet Jan, Taha A
Lu, Lu
Li, Cheng-Xiang
Williams, Robert W
Waters, Robert S
author_sort Jan, Taha A
collection PubMed
description BACKGROUND: Quantitative trait locus (QTL) mapping is an important tool for identifying potential candidate genes linked to complex traits. QTL mapping has been used to identify genes associated with cytoarchitecture, cell number, brain size, and brain volume. Previously, QTL mapping was utilized to examine variation of barrel field size in the somatosensory cortex in a limited number of recombinant inbred (RI) strains of mice. In order to further elucidate the underlying natural variation in mouse primary somatosensory cortex, we measured the size of the posterior medial barrel subfield (PMBSF), associated with the representation of the large mystacial vibrissae, in an expanded sample set that included 42 BXD RI strains, two parental strains (C57BL/6J and DBA/2J), and one F1 strain (B6D2F1). Cytochrome oxidase labeling was used to visualize barrels within the PMBSF. RESULTS: We observed a 33% difference between the largest and smallest BXD RI strains with continuous variation in-between. Using QTL linkage analysis from WebQTL, we generated linkage maps of raw total PMBSF and brain weight adjusted total PMBSF areas. After removing the effects of brain weight, we detected a suggestive QTL (likelihood ratio statistic [LRS]: 14.20) on the proximal arm of chromosome 4. Candidate genes under the suggestive QTL peak for PMBSF area were selected based on the number of single nucleotide polymorphisms (SNPs) present and the biological relevance of each gene. Among the candidate genes are Car8 and Rab2. More importantly, mRNA expression profiles obtained using GeneNetwork indicated a strong correlation between total PMBSF area and two genes (Adcy1 and Gap43) known to be important in mouse cortex development. GAP43 has been shown to be critical during neurodevelopment of the somatosensory cortex, while knockout Adcy1 mice have disrupted barrel field patterns. CONCLUSION: We detected a novel suggestive QTL on chromosome 4 that is linked to PMBSF size. The present study is an important step towards identifying genes underlying the size and possible development of cortical structures.
format Text
id pubmed-2254631
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-22546312008-02-27 Genetic analysis of posterior medial barrel subfield (PMBSF) size in somatosensory cortex (SI) in recombinant inbred strains of mice Jan, Taha A Lu, Lu Li, Cheng-Xiang Williams, Robert W Waters, Robert S BMC Neurosci Research Article BACKGROUND: Quantitative trait locus (QTL) mapping is an important tool for identifying potential candidate genes linked to complex traits. QTL mapping has been used to identify genes associated with cytoarchitecture, cell number, brain size, and brain volume. Previously, QTL mapping was utilized to examine variation of barrel field size in the somatosensory cortex in a limited number of recombinant inbred (RI) strains of mice. In order to further elucidate the underlying natural variation in mouse primary somatosensory cortex, we measured the size of the posterior medial barrel subfield (PMBSF), associated with the representation of the large mystacial vibrissae, in an expanded sample set that included 42 BXD RI strains, two parental strains (C57BL/6J and DBA/2J), and one F1 strain (B6D2F1). Cytochrome oxidase labeling was used to visualize barrels within the PMBSF. RESULTS: We observed a 33% difference between the largest and smallest BXD RI strains with continuous variation in-between. Using QTL linkage analysis from WebQTL, we generated linkage maps of raw total PMBSF and brain weight adjusted total PMBSF areas. After removing the effects of brain weight, we detected a suggestive QTL (likelihood ratio statistic [LRS]: 14.20) on the proximal arm of chromosome 4. Candidate genes under the suggestive QTL peak for PMBSF area were selected based on the number of single nucleotide polymorphisms (SNPs) present and the biological relevance of each gene. Among the candidate genes are Car8 and Rab2. More importantly, mRNA expression profiles obtained using GeneNetwork indicated a strong correlation between total PMBSF area and two genes (Adcy1 and Gap43) known to be important in mouse cortex development. GAP43 has been shown to be critical during neurodevelopment of the somatosensory cortex, while knockout Adcy1 mice have disrupted barrel field patterns. CONCLUSION: We detected a novel suggestive QTL on chromosome 4 that is linked to PMBSF size. The present study is an important step towards identifying genes underlying the size and possible development of cortical structures. BioMed Central 2008-01-07 /pmc/articles/PMC2254631/ /pubmed/18179704 http://dx.doi.org/10.1186/1471-2202-9-3 Text en Copyright © 2008 Jan et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Jan, Taha A
Lu, Lu
Li, Cheng-Xiang
Williams, Robert W
Waters, Robert S
Genetic analysis of posterior medial barrel subfield (PMBSF) size in somatosensory cortex (SI) in recombinant inbred strains of mice
title Genetic analysis of posterior medial barrel subfield (PMBSF) size in somatosensory cortex (SI) in recombinant inbred strains of mice
title_full Genetic analysis of posterior medial barrel subfield (PMBSF) size in somatosensory cortex (SI) in recombinant inbred strains of mice
title_fullStr Genetic analysis of posterior medial barrel subfield (PMBSF) size in somatosensory cortex (SI) in recombinant inbred strains of mice
title_full_unstemmed Genetic analysis of posterior medial barrel subfield (PMBSF) size in somatosensory cortex (SI) in recombinant inbred strains of mice
title_short Genetic analysis of posterior medial barrel subfield (PMBSF) size in somatosensory cortex (SI) in recombinant inbred strains of mice
title_sort genetic analysis of posterior medial barrel subfield (pmbsf) size in somatosensory cortex (si) in recombinant inbred strains of mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2254631/
https://www.ncbi.nlm.nih.gov/pubmed/18179704
http://dx.doi.org/10.1186/1471-2202-9-3
work_keys_str_mv AT jantahaa geneticanalysisofposteriormedialbarrelsubfieldpmbsfsizeinsomatosensorycortexsiinrecombinantinbredstrainsofmice
AT lulu geneticanalysisofposteriormedialbarrelsubfieldpmbsfsizeinsomatosensorycortexsiinrecombinantinbredstrainsofmice
AT lichengxiang geneticanalysisofposteriormedialbarrelsubfieldpmbsfsizeinsomatosensorycortexsiinrecombinantinbredstrainsofmice
AT williamsrobertw geneticanalysisofposteriormedialbarrelsubfieldpmbsfsizeinsomatosensorycortexsiinrecombinantinbredstrainsofmice
AT watersroberts geneticanalysisofposteriormedialbarrelsubfieldpmbsfsizeinsomatosensorycortexsiinrecombinantinbredstrainsofmice