S. Weigend et Sj. Lamont, Analysis of MHC class II and class IV restriction fragment length polymorphism in chicken lines divergently selected for multitrait immune response, POULTRY SCI, 78(7), 1999, pp. 973-982
In the present study, chickens of four lines divergently selected for high
(H) and low (L) immunocompetence in replicate were analyzed to investigate
polymorphisms of MHC class II and MHC class IV on the molecular level assoc
iated with selection. The long-term selection experiment for multitrait imm
unocompetence was carried out in replicates and allows, therefore, the oppo
rtunity to distinguish effects of selection from other genetic factors. The
SacI-digested DNA was hybridized individually with MHC class LI and MHC cl
ass IV gene probes. The MHC class II RFLP analysis revealed four polymorphi
c bands and only one of tl;em showed a significant difference between the s
election directions H and L pooled between replicates. The small frequency
differences of this band relative to the long-term selection suggest that t
his MHC class II fragment may contain genetic elements that are only slight
ly associated with the immune response traits used for selection. The hybri
dization with the MHC class IV probe displayed 26 scorable bands, of which
18 were polymorphic. Tn most instances, the differences between the lines w
ere likely caused by the influence of genetic factors other than selection
for multitrait immunocompetence. Only one band displayed a consistency in d
ifference between selection directions in both replicates and no frequency
difference between replicates. This band was almost completely absent in bo
th ii sublines, but at a frequency of about 50% in both L sublines. The gen
eral results of this study did not reveal major differences in band frequen
cies that indicate a close association of MHC class II and MHC class TV pol
ymorphic markers to the divergent selection for multitrait immune response.
Although the MHC makes a crucial contribution in immune response, it may h
ave been difficult to detect single-gene associations with the selection cr
iteria of this study, because of the myriad of components contributing to g
eneral immune responses measured in vivo.