New control elements of bacteriophage T4 pre-replicative transcription
Bacteriophage T4 pre-replicative genes are transcribed, by Escherichia coli RNA polymerase, in two alternative modes: an early mode and a middle mode. Middle mode transcription is under the control of at least one viral protein, p motA. We have identified two additional viral genes, motB and motC, t...
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Veröffentlicht in: | Journal of molecular biology 1985-03, Vol.182 (2), p.249-263 |
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description | Bacteriophage T4 pre-replicative genes are transcribed, by
Escherichia coli RNA polymerase, in two alternative modes: an early mode and a middle mode. Middle mode transcription is under the control of at least one viral protein, p
motA.
We have identified two additional viral genes,
motB and
motC, that map in the dispensable region of the T4 genome, between genes 39 and 56. p
motB and p
motC are diffusible factors which provide an alternative to the
motA dependent mode of middle transcription of many T4 genes.
Deletions of
motB and
motC are in fact lethal only in combination with a
motA mutant.
motB controls one of the alternative modes of transcription of the rIIA gene. When
motA or
motB are missing, transcription of rIIA is quantitatively unaffected; when both are missing the transcription rate drops by about 75%.
Control of transcription of the tRNA gene cluster is more complex. Transcription of subcluster 2 is maximally reduced (70%) only by deletions that, besides
motB, cut out an adjacent region. We guess that this adjacent region codes for an additional control element, which we call
motC.
The
motB gene is situated in a 750-base region between the left end-points of
del(39–56)-1 and -4. |
doi_str_mv | 10.1016/0022-2836(85)90343-2 |
format | Article |
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Escherichia coli RNA polymerase, in two alternative modes: an early mode and a middle mode. Middle mode transcription is under the control of at least one viral protein, p
motA.
We have identified two additional viral genes,
motB and
motC, that map in the dispensable region of the T4 genome, between genes 39 and 56. p
motB and p
motC are diffusible factors which provide an alternative to the
motA dependent mode of middle transcription of many T4 genes.
Deletions of
motB and
motC are in fact lethal only in combination with a
motA mutant.
motB controls one of the alternative modes of transcription of the rIIA gene. When
motA or
motB are missing, transcription of rIIA is quantitatively unaffected; when both are missing the transcription rate drops by about 75%.
Control of transcription of the tRNA gene cluster is more complex. Transcription of subcluster 2 is maximally reduced (70%) only by deletions that, besides
motB, cut out an adjacent region. We guess that this adjacent region codes for an additional control element, which we call
motC.
The
motB gene is situated in a 750-base region between the left end-points of
del(39–56)-1 and -4.</description><identifier>ISSN: 0022-2836</identifier><identifier>EISSN: 1089-8638</identifier><identifier>DOI: 10.1016/0022-2836(85)90343-2</identifier><identifier>PMID: 3999145</identifier><identifier>CODEN: JMOBAK</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Biological and medical sciences ; Fundamental and applied biological sciences. Psychology ; Genes, Regulator ; Genes, Viral ; Genetics ; Microbiology ; Mutation ; RNA, Transfer - biosynthesis ; RNA, Viral - biosynthesis ; T-Phages - genetics ; T-Phages - growth & development ; Time Factors ; Transcription, Genetic ; Viral Proteins - biosynthesis ; Virology</subject><ispartof>Journal of molecular biology, 1985-03, Vol.182 (2), p.249-263</ispartof><rights>1985</rights><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-ba0453c0ab405ee8f8ed387a341c3a2c84514e28aa7ba71680f2b34ab57864093</citedby><cites>FETCH-LOGICAL-c386t-ba0453c0ab405ee8f8ed387a341c3a2c84514e28aa7ba71680f2b34ab57864093</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0022-2836(85)90343-2$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8458305$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3999145$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pulitzer, John F.</creatorcontrib><creatorcontrib>Colombo, Mauro</creatorcontrib><creatorcontrib>Ciaramella, Maria</creatorcontrib><title>New control elements of bacteriophage T4 pre-replicative transcription</title><title>Journal of molecular biology</title><addtitle>J Mol Biol</addtitle><description>Bacteriophage T4 pre-replicative genes are transcribed, by
Escherichia coli RNA polymerase, in two alternative modes: an early mode and a middle mode. Middle mode transcription is under the control of at least one viral protein, p
motA.
We have identified two additional viral genes,
motB and
motC, that map in the dispensable region of the T4 genome, between genes 39 and 56. p
motB and p
motC are diffusible factors which provide an alternative to the
motA dependent mode of middle transcription of many T4 genes.
Deletions of
motB and
motC are in fact lethal only in combination with a
motA mutant.
motB controls one of the alternative modes of transcription of the rIIA gene. When
motA or
motB are missing, transcription of rIIA is quantitatively unaffected; when both are missing the transcription rate drops by about 75%.
Control of transcription of the tRNA gene cluster is more complex. Transcription of subcluster 2 is maximally reduced (70%) only by deletions that, besides
motB, cut out an adjacent region. We guess that this adjacent region codes for an additional control element, which we call
motC.
The
motB gene is situated in a 750-base region between the left end-points of
del(39–56)-1 and -4.</description><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes, Regulator</subject><subject>Genes, Viral</subject><subject>Genetics</subject><subject>Microbiology</subject><subject>Mutation</subject><subject>RNA, Transfer - biosynthesis</subject><subject>RNA, Viral - biosynthesis</subject><subject>T-Phages - genetics</subject><subject>T-Phages - growth & development</subject><subject>Time Factors</subject><subject>Transcription, Genetic</subject><subject>Viral Proteins - biosynthesis</subject><subject>Virology</subject><issn>0022-2836</issn><issn>1089-8638</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKxEAQRRtRdHz8gUIWIrqI9itJZSOI-ALRja6bSk9FWzLp2N2j-PdmnGGWrmpxz70Uh7FDwc8FF-UF51LmElR5CsVZzZVWudxgE8GhzqFUsMkma2SH7cb4wTkvlIZttq3quha6mLDbJ_rOrO9T8F1GHc2oTzHzbdagTRScH97xjbIXnQ2B8kBD5ywm90VZCthHG9yQnO_32VaLXaSD1d1jr7c3L9f3-ePz3cP11WNuFZQpb5DrQlmOjeYFEbRAUwUVKi2sQmlBF0KTBMSqwUqUwFvZKI1NUUGpea322Mlydwj-c04xmZmLlroOe_LzaKpSSC2gGkG9BG3wMQZqzRDcDMOPEdws9JmFG7NwY6Awf_qMHGtHq_15M6PpurTyNebHqxyjxa4dHVgX19j4Pyi-wC6XGI0uvhwFE62j3tLUBbLJTL37_49f5pqLAg</recordid><startdate>19850320</startdate><enddate>19850320</enddate><creator>Pulitzer, John F.</creator><creator>Colombo, Mauro</creator><creator>Ciaramella, Maria</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19850320</creationdate><title>New control elements of bacteriophage T4 pre-replicative transcription</title><author>Pulitzer, John F. ; Colombo, Mauro ; Ciaramella, Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-ba0453c0ab405ee8f8ed387a341c3a2c84514e28aa7ba71680f2b34ab57864093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Biological and medical sciences</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes, Regulator</topic><topic>Genes, Viral</topic><topic>Genetics</topic><topic>Microbiology</topic><topic>Mutation</topic><topic>RNA, Transfer - biosynthesis</topic><topic>RNA, Viral - biosynthesis</topic><topic>T-Phages - genetics</topic><topic>T-Phages - growth & development</topic><topic>Time Factors</topic><topic>Transcription, Genetic</topic><topic>Viral Proteins - biosynthesis</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pulitzer, John F.</creatorcontrib><creatorcontrib>Colombo, Mauro</creatorcontrib><creatorcontrib>Ciaramella, Maria</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pulitzer, John F.</au><au>Colombo, Mauro</au><au>Ciaramella, Maria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New control elements of bacteriophage T4 pre-replicative transcription</atitle><jtitle>Journal of molecular biology</jtitle><addtitle>J Mol Biol</addtitle><date>1985-03-20</date><risdate>1985</risdate><volume>182</volume><issue>2</issue><spage>249</spage><epage>263</epage><pages>249-263</pages><issn>0022-2836</issn><eissn>1089-8638</eissn><coden>JMOBAK</coden><abstract>Bacteriophage T4 pre-replicative genes are transcribed, by
Escherichia coli RNA polymerase, in two alternative modes: an early mode and a middle mode. Middle mode transcription is under the control of at least one viral protein, p
motA.
We have identified two additional viral genes,
motB and
motC, that map in the dispensable region of the T4 genome, between genes 39 and 56. p
motB and p
motC are diffusible factors which provide an alternative to the
motA dependent mode of middle transcription of many T4 genes.
Deletions of
motB and
motC are in fact lethal only in combination with a
motA mutant.
motB controls one of the alternative modes of transcription of the rIIA gene. When
motA or
motB are missing, transcription of rIIA is quantitatively unaffected; when both are missing the transcription rate drops by about 75%.
Control of transcription of the tRNA gene cluster is more complex. Transcription of subcluster 2 is maximally reduced (70%) only by deletions that, besides
motB, cut out an adjacent region. We guess that this adjacent region codes for an additional control element, which we call
motC.
The
motB gene is situated in a 750-base region between the left end-points of
del(39–56)-1 and -4.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>3999145</pmid><doi>10.1016/0022-2836(85)90343-2</doi><tpages>15</tpages></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Biological and medical sciences Fundamental and applied biological sciences. Psychology Genes, Regulator Genes, Viral Genetics Microbiology Mutation RNA, Transfer - biosynthesis RNA, Viral - biosynthesis T-Phages - genetics T-Phages - growth & development Time Factors Transcription, Genetic Viral Proteins - biosynthesis Virology |
title | New control elements of bacteriophage T4 pre-replicative transcription |
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