Differential expression of Iα- and IIα-globin genes in Norwegian dairy goats

Summary. Fast protein liquid chromatography (FPLC) and polyacrylamide gel electrophoresis were used to determine the ratio between ^Iα-and ^IIα-globin chains in Norwegian dairy goats. Three different phenotypes, designated normal (N) with ^Iα- to ^IIα-globin ratio 3:1, reversed (R) with ratio 1:2 and double-reversed (RR) with no ^Iα-globin, were described. Family studies indicated that the R animals were heterozygous, and the RR animal homozygous, for a haplotype without a functional ^Iα-globin product. Southern blot analysis of goat DNAs digested with six different restriction enzymes showed that the different ratios of α chain expression could not be due to a deletion of the ^Iα-gene and/or duplication or triplication of the ^IIα-globin genes. The homozygous reversed animal with no detectable ^Iα-globin had a mild anaemia.     

New embedding medium for sectioning undecalcified bone

Methylmethacrylate (MMA) is the most commonly used embedding medium for sectioning undecalcified bone; however, a number of problems exist with its use in a research laboratory. MMA requires a long infiltration time and temperature control, and it reacts with many polymers. We used Kleer Set resin™ as an alternative embedding medium for sectioning undecalcified bone specimens. Fluorochrome labeled bone specimens were sectioned transversely using a ground section technique and longitudinally on a sledge macrotome. The slides were viewed using both transmitted light and epifluorescence microscopy. High quality sections were obtained using Kleer Set resin™ for both sectioning techniques. We have shown that this new embedding medium is simpler, safer, quicker to use and does not interfere with visualization of fluorochromes.     

Restriction fragment length polymorphism of the caprine ß-globin gene cluster associated with the Hb ß-globin variants in Norwegian dairy goats

Restriction fragment length polymorphism (RFLP) analysis was used to characterize the beta-globin cluster in Norwegian dairy goats. In 122 individuals, different RFLP patterns were detected after BglII and PstI digestion and hybridization with a caprine beta-globin probe. The location of the polymorphic BglII and PstI sites were determined. The different RFLPs were in linkage disequilibrium with each other and with the beta-globin locus as studied at the protein level. A preferential association between certain RFLP haplotypes and beta-globin variants was observed. Polymorphic DNA fragments in the epsilon-globin genes were detected after MspI digestion and hybridization with a caprine epsilon-probe, and eight different band patterns were observed. Correlation between different MspI haplotypes and the beta-globin variants was determined.