Korean J Dermatol.  2004 May;42(5):536-544.

Differential Gene Expression Screening Between Black and Gray Hairs Using Subtractive Library and DNA Chip

Affiliations
  • 1Department of Dermatology, Kyungpook National University School of Medicine, Daegu, Korea. kimdw@knu.ac.kr
  • 2Department of Immunology, Kyungpook National University School of Medicine, Daegu, Korea.

Abstract

The identification of differential gene expression between gray and black hairs is an important study in modern hair pigment research. In this experiment, the authors have applied new methods by the integration of three updated molecular biological tools, T7 RNA polymerase-based RNA amplification, representational difference analysis (RDA), and microarray analysis, to screen the differentially expressed genes in gray and black hairs. The genes more abundantly expressed in black hairs were pigment related proteins, such as Pmel17, 95kD melanocyte-specific secreted glycoprotein, MART-1, tyrosinase, tyrosinase-related protein 1 etc. Also, expression of the selenium-binding protein (hSBP) gene and the spast gene for spastin protein were up-regulated in black hairs compared to those in gray hairs. In gray hairs, many kinds of genes related with keratin, trichohyalin and transmembrane glycoprotein were more expressed. In particular ch 17, hRPK.142_H_19 was expressed in gray hairs as high signal intensity.

Keyword

Gray hair; Subtractive library; DNA chip

MeSH Terms

DNA*
Gene Expression*
Glycoproteins
Hair*
Mass Screening*
Microarray Analysis
Monophenol Monooxygenase
Oligonucleotide Array Sequence Analysis*
RNA
DNA
Glycoproteins
Monophenol Monooxygenase
RNA
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