AI Article Synopsis

  • A study using a specific mouse intercross identified a region on chromosome 14 that affects cholesterol absorption based on gender.
  • Congenic animal studies showed that this region has multiple genetic factors leading to differing effects on cholesterol absorption in females compared to males.
  • Fine-mapping revealed a 6.3 Mb interval, where female subcongenic mice exhibited a 33% reduction in cholesterol absorption, linked to the candidate gene Ctsb, although further analysis suggested Ctsb might not be responsible for the observed effects.

Article Abstract

We used a mouse C57BL/6J×CASA/Rk intercross to map a locus on chromosome 14 that displayed a gender-dependent effect on cholesterol absorption from the intestine. Studies in congenic animals revealed a complex locus with multiple operating genetic determinants resulting in alternating gender-dependent phenotypic effects. Fine-mapping narrowed the locus to a critical 6.3 Mb interval. Female subcongenics, but not males, of the critical interval displayed a decrease of 33% in cholesterol absorption. RNA-Seq analysis of female subcongenic jejunum revealed that cysteine protease cathepsin B (Ctsb) is a candidate to explain the interval effect. Consistent with the phenotype in critical interval subcongenics, female Ctsb knockout mice, but not males, displayed a decrease of 31% in cholesterol absorption. Although studies in Ctsb knockouts revealed a gender-dependent effect on cholesterol absorption, further fine-mapping dismissed a role for Ctsb in determining the effect of the critical 6.3 Mb interval on cholesterol absorption.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617955PMC
http://dx.doi.org/10.1194/jlr.M034579DOI Listing

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