Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybrids. 1990

G Van Camp, and W Van Hul, and H Backhovens, and P Stinissen, and A Wehnert, and D Patterson, and A Vandenberghe, and C Van Broeckhoven
Department of Biochemistry, University of Antwerp, Belgium.

From a chromosome 21 phage library, we selected 10 clones located proximal of the senile plaque amyloid precursor protein gene. Since a locus for Alzheimer's disease (AD) has been localized in the pericentromeric region of chromosome 21, the selected phage clones are potential candidate probes for genetic analysis of AD. In this study, we subcloned single-copy fragments of the selected phage clones, refined their physical localization, and examined their chromosomal distribution in relation to their position on chromosome 21. The results indicated that the phage clones are identifying nine chromosome 21 loci, which, if polymorphic, may be helpful in localizing the AD locus more precisely. Moreover, since all phage clones are located close to the centromere of chromosome 21, they can be used to determine the parental origin of nondisjunction in trisomy 21 with high reliability.

UI MeSH Term Description Entries
D012150 Polymorphism, Restriction Fragment Length Variation occurring within a species in the presence or length of DNA fragment generated by a specific endonuclease at a specific site in the genome. Such variations are generated by mutations that create or abolish recognition sites for these enzymes or change the length of the fragment. RFLP,Restriction Fragment Length Polymorphism,RFLPs,Restriction Fragment Length Polymorphisms
D002503 Centromere The clear constricted portion of the chromosome at which the chromatids are joined and by which the chromosome is attached to the spindle during cell division. Centromeres
D002874 Chromosome Mapping Any method used for determining the location of and relative distances between genes on a chromosome. Gene Mapping,Linkage Mapping,Genome Mapping,Chromosome Mappings,Gene Mappings,Genome Mappings,Linkage Mappings,Mapping, Chromosome,Mapping, Gene,Mapping, Genome,Mapping, Linkage,Mappings, Chromosome,Mappings, Gene,Mappings, Genome,Mappings, Linkage
D002891 Chromosomes, Human, Pair 21 A specific pair of GROUP G CHROMOSOMES of the human chromosome classification. Chromosome 21
D003001 Cloning, Molecular The insertion of recombinant DNA molecules from prokaryotic and/or eukaryotic sources into a replicating vehicle, such as a plasmid or virus vector, and the introduction of the resultant hybrid molecules into recipient cells without altering the viability of those cells. Molecular Cloning
D005819 Genetic Markers A phenotypically recognizable genetic trait which can be used to identify a genetic locus, a linkage group, or a recombination event. Chromosome Markers,DNA Markers,Markers, DNA,Markers, Genetic,Genetic Marker,Marker, Genetic,Chromosome Marker,DNA Marker,Marker, Chromosome,Marker, DNA,Markers, Chromosome
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D006822 Hybrid Cells Any cell, other than a ZYGOTE, that contains elements (such as NUCLEI and CYTOPLASM) from two or more different cells, usually produced by artificial CELL FUSION. Somatic Cell Hybrids,Cell Hybrid, Somatic,Cell Hybrids, Somatic,Cell, Hybrid,Cells, Hybrid,Hybrid Cell,Hybrid, Somatic Cell,Hybrids, Somatic Cell,Somatic Cell Hybrid
D000544 Alzheimer Disease A degenerative disease of the BRAIN characterized by the insidious onset of DEMENTIA. Impairment of MEMORY, judgment, attention span, and problem solving skills are followed by severe APRAXIAS and a global loss of cognitive abilities. The condition primarily occurs after age 60, and is marked pathologically by severe cortical atrophy and the triad of SENILE PLAQUES; NEUROFIBRILLARY TANGLES; and NEUROPIL THREADS. (From Adams et al., Principles of Neurology, 6th ed, pp1049-57) Acute Confusional Senile Dementia,Alzheimer's Diseases,Dementia, Alzheimer Type,Dementia, Senile,Presenile Alzheimer Dementia,Senile Dementia, Alzheimer Type,Alzheimer Dementia,Alzheimer Disease, Early Onset,Alzheimer Disease, Late Onset,Alzheimer Sclerosis,Alzheimer Syndrome,Alzheimer Type Senile Dementia,Alzheimer's Disease,Alzheimer's Disease, Focal Onset,Alzheimer-Type Dementia (ATD),Dementia, Presenile,Dementia, Primary Senile Degenerative,Early Onset Alzheimer Disease,Familial Alzheimer Disease (FAD),Focal Onset Alzheimer's Disease,Late Onset Alzheimer Disease,Primary Senile Degenerative Dementia,Senile Dementia, Acute Confusional,Alzheimer Dementias,Alzheimer Disease, Familial (FAD),Alzheimer Diseases,Alzheimer Type Dementia,Alzheimer Type Dementia (ATD),Alzheimers Diseases,Dementia, Alzheimer,Dementia, Alzheimer-Type (ATD),Familial Alzheimer Diseases (FAD),Presenile Dementia,Sclerosis, Alzheimer,Senile Dementia
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia

Related Publications

G Van Camp, and W Van Hul, and H Backhovens, and P Stinissen, and A Wehnert, and D Patterson, and A Vandenberghe, and C Van Broeckhoven
January 1986, Cytogenetics and cell genetics,
G Van Camp, and W Van Hul, and H Backhovens, and P Stinissen, and A Wehnert, and D Patterson, and A Vandenberghe, and C Van Broeckhoven
January 1981, Cytogenetics and cell genetics,
G Van Camp, and W Van Hul, and H Backhovens, and P Stinissen, and A Wehnert, and D Patterson, and A Vandenberghe, and C Van Broeckhoven
November 1976, In vitro,
G Van Camp, and W Van Hul, and H Backhovens, and P Stinissen, and A Wehnert, and D Patterson, and A Vandenberghe, and C Van Broeckhoven
January 1997, Methods in molecular biology (Clifton, N.J.),
G Van Camp, and W Van Hul, and H Backhovens, and P Stinissen, and A Wehnert, and D Patterson, and A Vandenberghe, and C Van Broeckhoven
January 1992, Cytogenetics and cell genetics,
G Van Camp, and W Van Hul, and H Backhovens, and P Stinissen, and A Wehnert, and D Patterson, and A Vandenberghe, and C Van Broeckhoven
February 1993, American journal of human genetics,
G Van Camp, and W Van Hul, and H Backhovens, and P Stinissen, and A Wehnert, and D Patterson, and A Vandenberghe, and C Van Broeckhoven
January 1992, Cytogenetics and cell genetics,
G Van Camp, and W Van Hul, and H Backhovens, and P Stinissen, and A Wehnert, and D Patterson, and A Vandenberghe, and C Van Broeckhoven
January 1991, American journal of medical genetics,
G Van Camp, and W Van Hul, and H Backhovens, and P Stinissen, and A Wehnert, and D Patterson, and A Vandenberghe, and C Van Broeckhoven
August 1991, Genomics,
G Van Camp, and W Van Hul, and H Backhovens, and P Stinissen, and A Wehnert, and D Patterson, and A Vandenberghe, and C Van Broeckhoven
January 1993, Progress in clinical and biological research,
Copied contents to your clipboard!