Search

A sensitive and quantitative assay for DNA ligase has been developed which is suitable for the analysis of crude cell extracts of yeast. The assay is sufficiently sensitive to detect the low levels of DNA ligase activity remaining in cdc9 mutants of Saccharomyces cerevisiae. Indeed, we have been able to show that this residual activity is temperature-sensitive, thus establishing finally that CDC9 is the structural gene for DNA ligase.

Certain alfalfa plants can develop non-nitrogen fixing structures on their root systems when grown in testtubes under strictly axenic conditions. We demonstrate that these structures possess all the histological features characteristic of indeterminate nodules and that their formation is inhibited by combined nitrogen. The nodule morphogenesis-related gene ENOD2 is expressed in these nodules whereas leghemoglobin transcripts cannot be detected. The capacity to Nodulate in the Absence of Rhizobium (NAR) is maintained during clonal propagation of these alfalfa plants. Our results show that Rhizobium is not absolutely required for nodule morphogenesis and suggest that plant genetic determinants are involved in the NAR phenomenon.

A DNA sequence has been isolated from Schizosaccharomyces pombe which promotes high frequency transformation of plasmids in the same organism. It is closely linked to the DNA ligase gene CDC17 and has therefore been named ARS17 although in structure it differs substantially from ARS elements in Saccharomyces cerevisiae. ARS17 spans some 1.8 kb of DNA and deletion of any part of this region affects activity. Moreover, there does not appear to be any short sequence which is, by itself, sufficient for high frequency transformation. ARS17 lies between and partly overlaps two divergently transcribed genes and it is extremely AT rich. It lacks the consensus sequence found in S. cerevisiae ARSs and it has no ARS activity in S. cerevisiae.