Mapping of a single locus capable of complementing the defective heterochromatin phenotype of Roberts syndrome cells.

Abstract

Roberts syndrome (RS) is a developmental disorder characterized by tetraphocomelia and a broad spectrum of additional clinical features. Most patients with RS exhibit characteristic cytogenetic phenotypes, which include an abnormal appearance of pericentromeric heterochromatin on metaphase chromosomes, referred to as "heterochromatic repulsion." In the present study, we use complementation of this abnormal cytogenetic phenotype as a means to identify a specific region of the normal human genome capable of rendering phenotypic correction. We screened the entire human genome, using a transient chromosome-transfer assay, and demonstrated complementation exclusively after the transfer of proximal chromosome 8p, a result subsequently confirmed by stable microcell-mediated chromosome transfer. Additionally, homozygosity mapping was used to refine the interval of this complementing locus to 8p21. The results are consistent with the notion that the single gene defect responsible for heterochromatic splaying and developmental abnormalities maps to chromosome 8p21.

• Authors: Lisa D McDaniel, Darrell J Tomkins, Eric J Stanbridge, Martin J Somerville, Errol C Friedberg, Roger A Schultz
• Journal: American journal of human genetics (Am J Hum Genet) Vol. 77 Issue 1 Pg. 132-9 (Jul 2005) ISSN: 0002-9297 [Print] United States
• PMID: 15887093 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Heterochromatin

Topics

• Abnormalities, Multiple (genetics)
• Bone Diseases, Developmental (genetics)
• Chromosome Mapping
• Chromosomes, Human, Pair 8
• Craniofacial Abnormalities
• Genetic Complementation Test
• Heterochromatin (genetics)
• Homozygote
• Humans
• Phenotype
• Syndrome