Abstract:
:Several aspects of the terminal stages of T4 head maturation were investigated using ts and am mutants blocked at single steps of the assembly pathway. We had previously found that cells infected with mutants of gene 13, e.g., tsN38 and amE609, accumulated both stable (10 to 20%)- and fragile (80%)-filled head precursors (Hamilton and Luftig, 1972). Here we showed the following for such gene 13-defective, mutant-infected cells. (i) Using thin-section analysis the pool of phage precursor structures observed under nonpermissive conditions was one-third of that observed when the cells were cultured under permissive conditions. (ii) In order for complete conversion of the precursors into viable phage to occur, there were apparent requirements of metabolic energy, protein, and DNA synthesis. (iii) The intracellular DNA pool under nonpermissive conditions exhibited a 50% distribution between 63S (mature size) and 200 S (concatenate size) DNA, with the latter DNA serving as a precursor pool. Further, this DNA pool when spread onto a protein monolayer exhibited a dispersed array of DNA, strands around a core, which was less dense than that found for the greater than 1,000S DNA concatenate isolated from gene 49-defective infected cells. (iv) When precuations were taken to stabilize the head precursors, such as lysis of the cells into glutaraldehyde, there was a 30% increase in the yield of 1,200S filled heads. Correlating these results and previous results concerning gene 49-defective unfilled heads, we propose that there are several forms of gene 13 fragile head precursors which serve as intermediates between gene 49 unfilled heads and gene 13 stable filled heads. We cannot, however, rule out the possibility that all gene 13-defective heads represent a single class of unstable particles, which decay slowly. In either case, we have shown that gene 13-defective particles are unstable to some degree inside the cell and are highly unstable outside the cell; yet all particles can still be efficiently converted to phage in vivo.
journal_name
J Viroljournal_title
Journal of virologyauthors
Hamilton DL,Luftig RBdoi
10.1128/JVI.17.2.550-567.1976subject
Has Abstractpub_date
1976-02-01 00:00:00pages
550-67issue
2eissn
0022-538Xissn
1098-5514journal_volume
17pub_type
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pub_type: 杂志文章
doi:10.1128/JVI.40.1.133-141.1981
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pub_type: 杂志文章
doi:10.1128/JVI.44.3.1021-1030.1982
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pub_type: 杂志文章
doi:10.1128/JVI.17.2.642-658.1976
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.64.7.3471-3485.1990
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doi:10.1128/JVI.14.1.162-169.1974
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pub_type: 杂志文章
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pub_type: 杂志文章
doi:10.1128/jvi.77.6.3759-3767.2003
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journal_title:Journal of virology
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doi:10.1128/JVI.30.1.351-357.1979
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pub_type: 杂志文章
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pub_type: 杂志文章
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.39.1.60-66.1981
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.66.8.4803-4813.1992
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pub_type: 杂志文章
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journal_title:Journal of virology
pub_type: 杂志文章
doi:10.1128/JVI.5.2.99-108.1970
更新日期:1970-02-01 00:00:00
abstract::Many steps along the herpesvirus assembly and maturation pathway remain unclear. In particular, the acquisition of the virus tegument is a poorly understood process, and the molecular interactions involved in tegument assembly have not yet been defined. Previously we have shown that the two major herpes simplex virus ...
journal_title:Journal of virology
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