Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Transcriptional analysis of genes on human chromosome 21

Journal Article · · American Journal of Human Genetics
OSTI ID:134392
; ;  [1]
  1. Univ. of Michigan, Ann Arbor, MI (United States); and others

The polymerase chain reaction (PCR) was used to screen embryonic, fetal and adult human cDNA libraries for transcription on chromosome 21q22.1{yields}21q22.3. 73 pairs of oligonucleotide primers on chromosome 21 were applied to analyze 41 different cDNA libraries. Only phage eluate (and therefore no DNA isolation) was required for this sensitive screening. This technique was first used to demonstrate that huntingtin is expressed ubiquitiously throughout human life. 60 of the primers were positive with at least one library screening, indicating that the majority of primers derived from transcribed sequences. We examined embryonic (which we synthesized), fetal and adult human cDNA libraries. Even with our most complex human fetal brain library, we detected only ca. 50% of transcribed sequences, underscoring the need to screen multiple human cDNA libraries to determine if transcription occurred. Since only 2/73 clones were present in only one cDNA library, the vast majority of transcribed sequences are present in more than one tissue. Because this study involves random genes rather than genes selected because of their import, this demonstrates that only few anonymous genes are transcribed in a single tissue type. Expression of genes in different cDNA libraries aids in comparison between genotype and phenotype. Using combinations of gene-specific and vector-specific primers, we went on to develop a PCR-based technology that retrieves the largest sequences present in a cDNA library. This technology was used to isolate large genes on chromosome 21 that can be used in expression studies to examine the Down syndrome phenotype.

OSTI ID:
134392
Report Number(s):
CONF-941009--
Journal Information:
American Journal of Human Genetics, Journal Name: American Journal of Human Genetics Journal Issue: Suppl.3 Vol. 55; ISSN AJHGAG; ISSN 0002-9297
Country of Publication:
United States
Language:
English

Similar Records

Reverse transcription-polymerase chain reaction detection of transcribed sequences on human chromosome 21
Journal Article · Mon Mar 14 23:00:00 EST 1994 · Genomics; (United States) · OSTI ID:7062184

Cloning the cDNA of human PWP2, which encodes a protein with WD repeats and maps to 21q22.3
Journal Article · Mon Jul 15 00:00:00 EDT 1996 · Genomics · OSTI ID:469038

Down Syndome: A search for expressed sequences
Journal Article · Thu Sep 01 00:00:00 EDT 1994 · American Journal of Human Genetics · OSTI ID:134814