AI Article Synopsis

  • QTL mapping identified specific chromosomal regions linked to airway hyperresponsiveness in mice, focusing on A/J and C3H/HeJ strains.
  • Two significant loci were found on chromosomes 6 and 7, with the chromosome 6 locus confirming earlier studies.
  • A third suggestive linkage was observed on chromosome 17, indicating that multiple genetic factors influence airway responsiveness in these mouse strains.

Article Abstract

Quantitative trait locus (QTL) mapping was used to identify chromosomal regions contributing to airway hyperresponsiveness in mice. Airway responsiveness to methacholine was measured in A/J and C3H/HeJ parental strains as well as in progeny derived from crosses between these strains. QTL mapping of backcross [(A/J x C3H/HeJ) x C3H/HeJ] progeny (n = 137-227 informative mice for markers tested) revealed two significant linkages to loci on chromosomes 6 and 7. The QTL on chromosome 6 confirms the previous report by others of a linkage in this region in the same genetic backgrounds; the second QTL, on chromosome 7, represents a novel locus. In addition, we obtained suggestive evidence for linkage (logarithm of odds ratio = 1.7) on chromosome 17, which lies in the same region previously identified in a cross between A/J and C57BL/6J mice. Airway responsiveness in a cross between A/J and C3H/HeJ mice is under the control of at least two major genetic loci, with evidence for a third locus that has been previously implicated in an A/J and C57BL/6J cross; this indicates that multiple genetic factors control the expression of this phenotype.

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Source
http://dx.doi.org/10.1152/ajplung.1999.277.6.L1118DOI Listing

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