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Mapping of the spinal muscular atrophy (SMA) gene to a 750-kb interval flanked by two new microsatellites

  • B. Wirth
  • , A. El-Agwany
  • , A. Baasner
  • , A. Burghes
  • , A. Koch
  • , A. Dadze
  • , B. Piechaczeck-Wappenschmidt
  • , S. Rudnik-Schoneborn
  • , K. Zerres
  • , J. Schonling

Research output: Contribution to journalArticlepeer-review

Abstract

The gene for autosomal recessive proximal spinal muscular atrophy (SMA) has recently been mapped between D5S629 and D5S557. We report here a new single-locus microsatellite A31 (D5S823) and to multicopy microsatellites 97T-CA and 95/23-CA. The marker A31 maps to the region of overlap between YACs y116, y55 and y122, distal to D5S629; 97T-CA originates from a cosmid corresponding to the STS 97T, localized distally to A31, while 95/23-CA derives from a cosmid corresponding to the STS 97U, localized proximally to D5S557. We tested all our key recombinant families with these markers. In one type I/II SMA family, a recombinant was found that placed the SMA locus distal to D5S823. Homozygosity mapping in a consanguineous type I SMA family indicates that the SMA gene lies proximal to 95/23-CA. Thus, the two new markers, A31 and 95/23-CA further refine the SMA gene to an approximately 750-kb interval.

Original languageEnglish
Pages (from-to)56-60
Number of pages5
JournalEuropean Journal of Human Genetics
Volume3
Issue number1
DOIs
StatePublished - 1995

Keywords

  • Linkage analysis
  • Microsatellites
  • Multicopy markers
  • SMA
  • Spinal muscular atrophy

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