High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5.

Although autosomal recessive spinal muscular atrophy (SMA) has been mapped to chromosome 5q12-q13, there is for this region no genetic map based on highly informative markers. In this study we present the mapping of two previously reported microsatellite markers in 40 CEPH and 31 SMA pedigrees. We also describe the isolation of a new microsatellite marker at the D5S112 locus. The most likely order of markers (with recombination fractions given in parentheses) is 5cen-D5S6-(.02)-D5S125-(.04)-(JK53CA1/2,D5S11 2)-(.04)-D5S39-qter. The relative order of D5S6, D5S112, and D5S39 was confirmed by in situ hybridization. Multipoint linkage analysis in 31 SMA families indicates that the SMA locus lies in the 6-cM interval between D5S6 and JK53CA1/2, D5S112.

[1]  J. Ott,et al.  Linkage analysis of spinal muscular atrophy. , 1992, Genomics.

[2]  S. Knight,et al.  Molecular heterogeneity of the fragile X syndrome. , 1991, Nucleic acids research.

[3]  A. Roche,et al.  A YAC contig across the fragile X site defines the region of fragility. , 1991, Nucleic acids research.

[4]  A. Monaco,et al.  Yeast artificial chromosome libraries containing large inserts from mouse and human DNA. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[5]  H. Gurling,et al.  Two microsatellite polymorphisms at the D5S39 locus. , 1991, Nucleic acids research.

[6]  G. Lathrop,et al.  Linkage analysis in spinal muscular atrophy, by six closely flanking markers on chromosome 5. , 1991, American journal of human genetics.

[7]  J. Weber Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms. , 1990, Genomics.

[8]  T. Lehner,et al.  Genetic homogeneity between acute and chronic forms of spinal muscular atrophy , 1990, Nature.

[9]  M. Lathrop,et al.  Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q , 1990, Nature.

[10]  M. Leppert,et al.  Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3 , 1990, Nature.

[11]  H. Cann,et al.  Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome. , 1990, Genomics.

[12]  N. Freimer,et al.  Deletion mapping of DNA markers to a region of chromosome 5 that cosegregates with schizophrenia. , 1989, Genomics.

[13]  D. Ledbetter,et al.  Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[14]  R. Ferrell,et al.  Report of the committee on the genetic constitution of chromosome 5. , 1988, Cytogenetics and cell genetics.

[15]  E. Lander,et al.  Construction of multilocus genetic linkage maps in humans. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[16]  J. Ott,et al.  Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. , 1985, American journal of human genetics.