Genetic linkage map of human chromosome 21. 1988

R E Tanzi, and J L Haines, and P C Watkins, and G D Stewart, and M R Wallace, and R Hallewell, and C Wong, and N S Wexler, and P M Conneally, and J F Gusella
Neurogenetics Laboratory, Massachusetts General Hospital, Boston.

Two of the most common disorders affecting the human nervous system, Down syndrome and Alzheimer's disease, involve genes residing on human chromosome 21. A genetic linkage map of human chromosome 21 has been constructed using 13 anonymous DNA markers and cDNAs encoding the genes for superoxide dismutase 1 (SOD1) and the precursor of Alzheimer's amyloid beta peptide (APP). Segregation of restriction fragment length polymorphisms (RFLPs) for these genes and DNA markers was traced in a large Venezuelan kindred established as a "reference" pedigree for human linkage analysis. The 15 loci form a single linkage group spanning 81 cM on the long arm of chromosome 21, with a markedly increased frequency of recombination occurring toward the telomere. Consequently, 40% of the genetic length of the long arm corresponds to less than 10% of its cytogenetic length, represented by the terminal half of 21q22.3. Females displayed greater recombination than males throughout the linkage group, with the difference being most striking for markers just below the centromere. Definition of the linkage relationships for these chromosome 21 markers will help refine the map position of the familial Alzheimer's disease gene and facilitate investigation of the role of recombination in nondisjunction associated with Down syndrome.

UI MeSH Term Description Entries
D008040 Genetic Linkage The co-inheritance of two or more non-allelic GENES due to their being located more or less closely on the same CHROMOSOME. Genetic Linkage Analysis,Linkage, Genetic,Analyses, Genetic Linkage,Analysis, Genetic Linkage,Genetic Linkage Analyses,Linkage Analyses, Genetic,Linkage Analysis, Genetic
D008126 Lod Score The total relative probability, expressed on a logarithmic scale, that a linkage relationship exists among selected loci. Lod is an acronym for "logarithmic odds." Lod Scores,Score, Lod,Scores, Lod
D008297 Male Males
D008957 Models, Genetic Theoretical representations that simulate the behavior or activity of genetic processes or phenomena. They include the use of mathematical equations, computers, and other electronic equipment. Genetic Models,Genetic Model,Model, Genetic
D010375 Pedigree The record of descent or ancestry, particularly of a particular condition or trait, indicating individual family members, their relationships, and their status with respect to the trait or condition. Family Tree,Genealogical Tree,Genealogic Tree,Genetic Identity,Identity, Genetic,Family Trees,Genealogic Trees,Genealogical Trees,Genetic Identities,Identities, Genetic,Tree, Family,Tree, Genealogic,Tree, Genealogical,Trees, Family,Trees, Genealogic,Trees, Genealogical
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
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
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

R E Tanzi, and J L Haines, and P C Watkins, and G D Stewart, and M R Wallace, and R Hallewell, and C Wong, and N S Wexler, and P M Conneally, and J F Gusella
January 1985, Annals of the New York Academy of Sciences,
R E Tanzi, and J L Haines, and P C Watkins, and G D Stewart, and M R Wallace, and R Hallewell, and C Wong, and N S Wexler, and P M Conneally, and J F Gusella
May 1989, Genomics,
R E Tanzi, and J L Haines, and P C Watkins, and G D Stewart, and M R Wallace, and R Hallewell, and C Wong, and N S Wexler, and P M Conneally, and J F Gusella
March 1991, Genomics,
R E Tanzi, and J L Haines, and P C Watkins, and G D Stewart, and M R Wallace, and R Hallewell, and C Wong, and N S Wexler, and P M Conneally, and J F Gusella
November 1992, Genomics,
R E Tanzi, and J L Haines, and P C Watkins, and G D Stewart, and M R Wallace, and R Hallewell, and C Wong, and N S Wexler, and P M Conneally, and J F Gusella
January 1993, Progress in clinical and biological research,
R E Tanzi, and J L Haines, and P C Watkins, and G D Stewart, and M R Wallace, and R Hallewell, and C Wong, and N S Wexler, and P M Conneally, and J F Gusella
January 1993, Genomics,
R E Tanzi, and J L Haines, and P C Watkins, and G D Stewart, and M R Wallace, and R Hallewell, and C Wong, and N S Wexler, and P M Conneally, and J F Gusella
January 1993, Genomics,
R E Tanzi, and J L Haines, and P C Watkins, and G D Stewart, and M R Wallace, and R Hallewell, and C Wong, and N S Wexler, and P M Conneally, and J F Gusella
November 1985, Science (New York, N.Y.),
R E Tanzi, and J L Haines, and P C Watkins, and G D Stewart, and M R Wallace, and R Hallewell, and C Wong, and N S Wexler, and P M Conneally, and J F Gusella
September 1987, Genomics,
R E Tanzi, and J L Haines, and P C Watkins, and G D Stewart, and M R Wallace, and R Hallewell, and C Wong, and N S Wexler, and P M Conneally, and J F Gusella
November 1989, Genomics,
Copied contents to your clipboard!