Haston Christina K, Tsui Lap-Chee
Program of Genetics and Genomic Biology, Research Institute, The Hospital for Sick Children, and Department of Molecular and Medical Genetics, University of Toronto, Ontario, Canada.
Physiol Genomics. 2003 Jan 15;12(2):79-84. doi: 10.1152/physiolgenomics.00114.2002.
The strain-dependent survival of cystic fibrosis (CF) knockout mice has been used to map a modifier of CF, Cfm1, in mice and, subsequently, in humans. To identify additional modifiers of the CF phenotype, in this study, the survival of F2 CF mice derived from a cross between congenic C57BL/6J CF and BALB/cJ CF heterozygotes was followed up to 12 wk of age. A genome-wide linkage scan completed in F2 CF mice revealed a chromosome 10 locus (P = 1.2 x 10(-4)) to predict for intestinal distress in CF male mice. An X chromosome locus for which non-Mendelian inheritance favoring B6 alleles in the surviving CF mice and BALB alleles in mice of a control population, was identified. The survival of female mice, both F2 CF and F2 control, was linked to loci on chromosomes 3 and 5. The identification of additional putative CF modifier loci may permit further genetic dissection of the complex CF phenotype.
囊性纤维化(CF)基因敲除小鼠的品系依赖性存活已被用于在小鼠中定位CF修饰基因Cfm1,随后也在人类中进行了定位。为了鉴定CF表型的其他修饰基因,在本研究中,对来自同源C57BL/6J CF和BALB/cJ CF杂合子杂交的F2 CF小鼠的存活情况进行了跟踪,直至12周龄。在F2 CF小鼠中完成的全基因组连锁扫描揭示了一个位于10号染色体的位点(P = 1.2 x 10(-4)),可预测CF雄性小鼠的肠道不适。还鉴定了一个X染色体位点,在存活的CF小鼠中,非孟德尔遗传倾向于B6等位基因,而在对照群体的小鼠中则倾向于BALB等位基因。F2 CF雌性小鼠和F2对照雌性小鼠的存活与3号和5号染色体上的位点有关。鉴定出其他假定的CF修饰基因位点可能有助于对复杂的CF表型进行进一步的基因剖析。