Abstract
Nuclei prepared from mouse submandibular salivary gland show marked fragility during isolation. Intact nuclei relatively free from cytoplasmic contamination were obtained by homogenization in buffers containing 0.88 M sucrose, Ca2+, spermine, spermidine and the proteinase inhibitor aprotinin, followed by centrifugation through 2.2 M sucrose. The kinetics of digestion by the micrococcal nuclease of chromatin in these nuclei are similar to those of chromatin from mouse liver nuclei. Base-pair size analysis of the solubilized DNA from both organs shows a stable high MW species of chromatin, which is further digested to mononucleosome and subnucleosome species. With extensive digestion the chromatin becomes insoluble. The mononucleosomes produced from salivary gland chromatin after the inhibition of endogenous proteinase activity exhibit an s20,W value of 11S and contain histones H1, H2A, H2B, H3 and H4.