"The Pattern of Gene Expression in Human CD15 + Myeloid Progenitor Cells".
Sanggyu Lee*, Guolin Zhou*, Terry Clark 1, Jianjun Chen*, Janet D. Rowley*, and San Ming Wang* 2,
Departments of * Medicine and 1 Computer Science,
University of Chicago
Medical Center, 5841 South Maryland, MC2115, Chicago, IL 60637
2 To whom reprint requests should be addressed. E-mail: swang1@midway.uchicago.edu
We performed a genome-wide analysis of gene expression in primary
human CD15 + myeloid progenitor cells. By using the serial analysis
of gene expression (SAGE) technique, we obtained quantitative information
for the expression of 37,519 unique SAGE-tag sequences. Of these unique
tags, (i) 25% were detected at high and intermediate levels, whereas 75%
were present as single copies, (ii) 53% of the tags matched known expressed
sequences, 34% of which were matched to more than one known expressed sequence,
and (iii) 47% of the tags had no matches and represent potentially novel
genes. The correct genes were confirmed by application of the generation
of longer cDNA fragments from SAGE tags for gene identification (GLGI)
technique for high-copy tags with multiple matches. A set of genes known
to be important in myeloid differentiation were expressed at various levels
and used different spliced forms. This study provides a normal baseline
for comparison of gene expression in myeloid diseases. The strategy of
using SAGE and GLGI
techniques in this study has broad applications to the genome-wide
identification of expressed genes.
1. "Ultrastructural Probes of DNA Templates within Human Bone Marrow and Lymph Node Cells".
2. "Activity
of DNA Templates During Cell Division and Cell Differentiation".
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