TY - JOUR
T1 - Interspecific resources: a major tool for quantitative trait locus cloning and speciation research
AU - Laissue Hormaza, Paul
AU - L'Hôte, David
AU - Serres, Catherine
AU - Montagutelli, Xavier
AU - Veitia, Reiner A.
AU - Vaiman, Daniel
PY - 2010/1/20
Y1 - 2010/1/20
N2 - Positional cloning of the quantitative trait locus (QTL) still encounters numerous difficulties, which explains why thousands of QTL have been mapped, while only a few have been identified at the molecular level. Here, we focus on a specific mapping tool that exists in plant and animal model species: interspecific recombinant congenic strains (IRCSs) or interspecific nearly isogenic lines (NILs). Such panels exhibit a much higher sequence diversity than intraspecific sets, thus enhancing the contrasts between phenotypes. In animals, it allows statistical significance to be reached even when using a limited number of individuals. Therefore, we argue that interspecific resources may constitute a major genetic tool for positional cloning and for understanding some bases of speciation mechanisms.
AB - Positional cloning of the quantitative trait locus (QTL) still encounters numerous difficulties, which explains why thousands of QTL have been mapped, while only a few have been identified at the molecular level. Here, we focus on a specific mapping tool that exists in plant and animal model species: interspecific recombinant congenic strains (IRCSs) or interspecific nearly isogenic lines (NILs). Such panels exhibit a much higher sequence diversity than intraspecific sets, thus enhancing the contrasts between phenotypes. In animals, it allows statistical significance to be reached even when using a limited number of individuals. Therefore, we argue that interspecific resources may constitute a major genetic tool for positional cloning and for understanding some bases of speciation mechanisms.
U2 - 10.1002/bies.200900027
DO - 10.1002/bies.200900027
M3 - Research Article
SN - 0265-9247
VL - 32
SP - 132
EP - 142
JO - BioEssays
JF - BioEssays
IS - 2
ER -