Immunological detection of left-handed Z DNA in isolated polytene chromosomes. Effects of ionic strength, pH, temperature and topological stress.

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Abstract
We have searched for the presence of left‐handed Z DNA in unfixed polytene chromosomes isolated from the salivary glands of Chironomus thummi larvae. Physiological as well as fixation conditions were explored to assess the effects of a variety of factors known to influence the B‐Z equilibrium. At neutral pH and physiological ionic strength, a weak immunofluorescence staining confined to the periphery of chromosomal bands is elicited but only by using high concentrations of anti‐Z DNA immunoglobulin (IgG). The accessibility of internal highly condensed structures, as monitored with antibodies against core histones, is very limited under these conditions. Increasing the ionic strength exposes core histone determinants but results in a decondensation of the bands. The staining for Z DNA is still weak and primarily restricted to regions resisting decondensation or undergoing collapse. Dramatic changes in anti‐Z DNA immunofluorescence intensities occur upon short exposure to low pH. Adjustment of the pH between 2.5 and 2.0 leads to an abrupt large increase in antibody binding, at first confined to a few specific bands and then generalized to bands throughout the chromosomes in a pattern very similar to that elicited in classical acid‐fixed squash preparations. The acid‐mediated effects are influenced by ionic strength, temperature and prior removal of histones; they can be mimicked by exposure to high temperature at neutral pH. The ‘transition pH’ assessed with a monoclonal IgG specific for left‐handed d(G‐C)n sequences is slightly lower than in the case of polyclonal antibodies which also recognize d(A‐C)n X d(G‐T)n.(ABSTRACT TRUNCATED AT 400 WORDS)