Improved iron-hematoxylin stain for elastic fibers

A modification of Verhoeff's elastic tissue stain with connective tissue counterstaining is described. The modified procedure requires no differentiation of the elastic fibers, thus eliminating the problem of over- or understaining of elastic fibers. The procedure is easy to perform and yields consistently good results with sharply defined elastic fibers that are easily distinguishable from other connective tissue elements. It is recommended for routine use, particularly when photomicrography is desired.     

Oxygen and Guanine–Cytosine Profiles in Marine Environments

One of the historic debates in molecular evolution concerns the strong variation in the genomic guanine–cytosine (GC) content of prokaryotes, which ranges from approximately 20–75%: Is this factor selectively neutral, or is it the result of natural selection? In a previous article published by our group, we showed that inside well-defined taxonomic groups of prokaryotes, strictly aerobic organisms tend to display higher genomic GC levels than strictly anaerobic species. In the present study, we examined the GC content of fragments of DNA obtained from microbial communities along a well-defined environmental gradient: a 4,000-m vertical profile in the North Pacific subtropical gyre. The patterns of GC distribution might be associated with oxygen concentrations in the seawater column. These results give further support to the link between a physiologic trait (aerobic respiration) and genomic GC content.     

Genetic and morphometric studies of the heterogeneity in the testicular defect of the Hre rat and the interaction between the Hre and grc genes

This study was undertaken to examine further the behavior of the Hre gene and its interaction with the growth and reproduction complex genes (grc) in the (Hre x BN)F2, Hre x (Hre x BN)F1 and (BIL/1 x Hre) F2 crosses. The blaze characteristic of rats carrying the Hre gene was linked to testicular weight but not to the body weight or to the major histocompatibility complex (MHC). The Hre defect was genetically unrelated to the testicular defect caused by the grc. The Hre gene had a variable effect on the testes of the rats in different crosses, and it could be categorized into three distinct stages of progressively greater severity. In the cross in which the parents carried the Hre/+ and grc/grc genes, respectively, there was a decreased litter size, an increased male:female ratio in the offspring and poor reproductive performance when compared to a similar cross in which the Hre/+ gene alone was segregating. There was, however, no effect on the severity of the testicular defect. Thus, the grc can interact with the Hre gene to cause embryonic death, which appears to be selective for females, but not to influence the severity of the testicular defect.     

Genetic variations in human testosterone-estradiol binding globulin

The human testosterone-estradiol-binding globulin (hTeBG) is a plasma heterogeneous glycoprotein with high affinity for a number of circulating steroid hormones. The heterogeneity originates from differential glycosylation of a common protein precursor. Analysis of desialylated hTeBG by isoelectric focusing (IEF) has revealed that microheterogeneity could be partly attributed to variability in sialic acid content or rearrangement of amino acid composition. We have studied this possibility by the analysis of desialylated serum hTeBG by Western blotting of proteins previously separated on IEF-gels. Two distinct well-defined IEF patterns were identified. The most frequent consisted of two major IEF-bands of equal color intensity. The other pattern consisting of four IEF-bands was present in only 5.55% of the total serum samples analyzed. Family studies showed that these phenotypes were autosomally inherited with a simple Mendelian transmission and allele frequencies had an excellent agreement between the observed and expected phenotypes. Androgen affinity constants and serum concentrations of hTeBG variant were similar to those of normal hTeBG. Molecular analyses of each of the exons of hTeBG gene by denaturing gradient gel electrophoresis revealed the presence of a point mutation in exon 8. The studies presented herein confirm and extend previous reports on the existence of structural variants of hTeBG. In addition, the mutation reported in this study is probably the same as that recently identified within numerous ethnic groups throughout the world, thus further supporting the concept of a two allele gene worldwide concoding hTeBG.