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E-MEXP-258 transcription profiling by array Homo sapiens

Transcription profiling of human NF1 heterozygous (NF1+/-) melanocytes from a Neurofibromatosis type 1 patient and NF1 wild type (NF1+/+) melanocytes of a healthy control patient

·Released Feb. 5, 2005 ·Updated May 2, 2014
4
Samples
8
Assays
1
Array Platforms
1
References
Description

One of the major primary features of the neurocutaneous genetic disorder Neurofibromatosis type 1 are the hyperpigmentary café-au-lait macules where dysregulation of melanocyte development, proliferation and differentiation is considered to play a key etiopathogenic role. To gain better insight in the possible role of the tumor suppressor gene NF1, a transcriptomic microarray analysis was performed on human NF1 heterozygous (NF1+/-) melanocytes of a Neurofibromatosis type 1 patient and NF1 wild type (NF1+/+) melanocytes of a healthy control patient, both cultured from normally pigmented and hyperpigmented lesional café-au-lait skin. Out of 13,850 unique genes, a total of 137 had a significant twofold or more up- (72) or down-regulated (65) expression in NF1+/- melanocytes compared to NF1+/+ melanocytes (genotype effect). Considering possible intrinsic genetic variation in lesional skin, melanocytes showed a total of 51 genes having a significant twofold or more up- (37) or down-regulated (14) expression when they were cultured from hyperpigmentary café-au-lait skin compared to normally pigmented skin (lesional skin type effect). NF1+/- café-au-lait skin melanocytes showed 468 genes with a significant two-fold or more up- (183) or down-regulated (285) expression going beyond the sum of the separate main effects (interaction). Detailed analysis enabled the identification of several modulated genes in NF1+/- (café-au-lait skin) melanocytes, mainly involved in controlling cell proliferation and cell maintenance, in cell adhesion and, surprisingly, in the immune response. An interesting finding was that a high number of transcription factor genes were differentially modulated, among which a specific subset - important in melanocyte-lineage development - showed downregulation in a transcriptional cis-regulatory network governing the activation of the melanocyte-specific dopachrome tautomerase (DCT) gene.

Array Platforms
A-MEXP-146
VIB Human 21K 1(8 items)
Sample Attributes
BioSourceType
biopsy
DevelopmentalStage
adult
DiseaseState
neurofibromatosis type 1
IndividualGeneticCharacteristics
NF1 heterozygous
Organism
Homo sapiens
TargetedCellType
melanocytes
Experiment Info
Accession
E-MEXP-258
Type
transcription profiling by array
Organism
Homo sapiens
Released
Feb. 5, 2005
Updated
May 2, 2014
Submitter
Jean-Marie Naeyaert、 Sofie De Schepper、 Marnik Vuylsteke、 Paul Van Hummelen、 Joachim Boucneau、 Jo Lambert
External Links
ArrayExpress source
Analysis Services
Analysis Services

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