Tissue Distlibution of the EMB-S protein during development Kiyoji Nishiwaki, Tohru Sano, Yo Tabuse, and Johji Miwa Fundamental Research Laboratories, NEC Corporation, Miyukigaoka, Tsukuba 305, Japan The
emb-5 gene is required for the correct timing of gut precursor cell division during gastrulation' 2 and for the proliferation of germ cells during postembryonic development3. emb 5 encodes the protein EMB-5 homologous to the yeast nuclear protein SPT6, which has been shown to affect the transcription of a variety of genes and suggested to play a role in chromatin assembly or modification4. To understand the tissue distribution patten of EMB-5 during development, we have conducted the epitope-tagging analysis using the antigenic epitope of hemagglutinin of influenza virus (HA I ). The
emb-5 gene epitope-tagged at the 5' end was active and rescued the
emb-5 mutant phenotype although more weakly than did the wild type gene. Using a strain with chromosomally integrated DNA(epitope tagged
emb-5 +
rol-6d), we found that the anti-epitope antibodies stained interphase nuclei of various cell types, although they did not stain early embryonic cells before the 5 l-cell stage and germ cells in all stages including mature oocytes and sperm. (We used the polyclonal HA. 11 antibody from BAbCO because the monoclonal antibody 12CA5 from Boehringer gave substantial background staining of worm nuclei.) On the other hand, the antibodies against an EMB-5 C-terminal peptide stained all the interphase nuclei except for the germ cell nuclei before the adult stage in the same strain, although the mature sperm were not stained as in the case of the anti-epitope antibodies. In embryos, the germline precursor cells P0 to P3 appeared to be stained but not the germline cells P4, Z2, and Z3. These results suggest that EMB-5 may have modifications on its N-terminus in early embryonic cells and adult germ cells, and that it may have modifications on both of its N- and C-termini or not be present in germ cells before the adult stage and mature sperm. It is possible that EMB-5 is not required for the mature sperm lacking chromatin proteins. It is interesting that the early embryonic cells and germ cells, where the temperature-sensitive
emb-5 mutations show remarkable effects, seem to have modified EMB-5 proteins. However, because we are analyzing the artificially introduced epitope-tagged gene, we have to be careful in interpreting its expression pattem. We are currently preparing antibodies against an N-terminal peptide and several internal peptides of EMB-5. 1. Miwa et al. (1980). Dev. Biol. 76, 160-174. 2. Schierenberg et al.(
l980). Dev. Biol.76, 141-159. 3. Nishiwaki, Miwa, and Hedgecock, unpublished. 4. Nishiwaki eJ al. (1993). Mol. Gen. Genet. 239, 313-322.