Differential regulation of insect globin and actin mRNAs during larval development in Chironomus thummi

S1 nuclease protection assays were used to measure changes in the steady-state levels of six different globin ( Gb) mRNAs in the midge, Chironomus thummi thummi ( C. thummi, Diptera) during larval development. Two distinct patterns of change were observed. GbI, IV, VIIB-4 and VIIB-5 transcripts were...

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Veröffentlicht in:Gene 1991-05, Vol.101 (2), p.215-222
Hauptverfasser: Saffarini, Daad A., Trewitt, Patrick M., Luhm, Robert A., Bergtrom, Gerald
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creator Saffarini, Daad A.
Trewitt, Patrick M.
Luhm, Robert A.
Bergtrom, Gerald
description S1 nuclease protection assays were used to measure changes in the steady-state levels of six different globin ( Gb) mRNAs in the midge, Chironomus thummi thummi ( C. thummi, Diptera) during larval development. Two distinct patterns of change were observed. GbI, IV, VIIB-4 and VIIB-5 transcripts were present in 3rd instar larvae, rose from low levels immediately post-moult to peak levels by day 2–3 of the 4th instar, and then declined, reaching near-basal levels by day 7–8. In contrast, transcripts of GbIII (known from previous studies to be 4th instar-specific) and VI, which were undetectable in the 3rd instar, rose to high levels by day 2 of the 4th instar, but remained elevated thereafter. Our data further showed that closely linked Gb genes were not necessarily expressed in a coordinate manner. Unlike the Gb mRNAs, actin ( Act) mRNA levels (measured by slot-blot hybridization to a heterologous probe) increased progressively as a proportion of total RNA during 4th instar development. Therefore, the regulation of C. thummi Gb transcript levels is specific, differing from that of Act and among the Gb mRNAs themselves. Elevated 20-hydroxyecdysone (HE) titer at the 3rd-4th instar moult correlates with the low steady-state levels of Gb mRNAs immediately post-moult. However, other aspects of Gb mRNA profiles cannot be explained on the basis of a direct repressive effect by HE on Gb gene transcription.
doi_str_mv 10.1016/0378-1119(91)90414-7
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Two distinct patterns of change were observed. GbI, IV, VIIB-4 and VIIB-5 transcripts were present in 3rd instar larvae, rose from low levels immediately post-moult to peak levels by day 2–3 of the 4th instar, and then declined, reaching near-basal levels by day 7–8. In contrast, transcripts of GbIII (known from previous studies to be 4th instar-specific) and VI, which were undetectable in the 3rd instar, rose to high levels by day 2 of the 4th instar, but remained elevated thereafter. Our data further showed that closely linked Gb genes were not necessarily expressed in a coordinate manner. Unlike the Gb mRNAs, actin ( Act) mRNA levels (measured by slot-blot hybridization to a heterologous probe) increased progressively as a proportion of total RNA during 4th instar development. Therefore, the regulation of C. thummi Gb transcript levels is specific, differing from that of Act and among the Gb mRNAs themselves. Elevated 20-hydroxyecdysone (HE) titer at the 3rd-4th instar moult correlates with the low steady-state levels of Gb mRNAs immediately post-moult. 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Elevated 20-hydroxyecdysone (HE) titer at the 3rd-4th instar moult correlates with the low steady-state levels of Gb mRNAs immediately post-moult. 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Psychology</subject><subject>gb gene</subject><subject>genbank/m57410</subject><subject>genbank/m57411</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>genetic regulation</subject><subject>globin mRNA accumulation</subject><subject>globins</subject><subject>Globins - genetics</subject><subject>Larva - metabolism</subject><subject>larvae</subject><subject>messenger RNA</subject><subject>midge</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Molecular Sequence Data</subject><subject>multigene family</subject><subject>Recombinant DNA</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>S1 nuclease protection</subject><subject>Single-Strand Specific DNA and RNA Endonucleases - metabolism</subject><issn>0378-1119</issn><issn>1879-0038</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUuLFDEUhYMoYzv6DxSzUXRRmlSq8tgIQ8_4gEFBnXVIJzc1kaqkTaoa_Pem7GbcaTY3cL9zuJyD0FNK3lBC-VvChGwopeqVoq8V6WjXiHtoQ6VQDSFM3kebO-QhelTKD1Jf37dn6Kyts5Nig4bL4D1kiHMwI84wLKOZQ4o4eRxiATvjYUy7ELGJDhs719_09fNFwW7JIQ54NPlQlQ4OMKb9VI2qDm9vQ04xTUvB8-0yTeExeuDNWODJaZ6jm_dX37cfm-svHz5tL64by3oxN6wTQBQlku5axpWStuudAwfC9KITQnEnnOOeWCCe-Z2RAiwRjnILBiRj5-jl0Xef088FyqynUCyMo4mQlqIl4Yxz9X-Q8p6LvhUV7I6gzamUDF7vc5hM_qUp0WsRek1ZrylrRfWfIvQqe3byX3YTuDvRKfm6f3Ham2LN6LOJNpS_3kp0StCucs-PnDdJmyFX5uZbSygjVDAu1er07khAzfUQIOtiA0QLLuTan3Yp_PvU35A4rpo</recordid><startdate>19910530</startdate><enddate>19910530</enddate><creator>Saffarini, Daad A.</creator><creator>Trewitt, Patrick M.</creator><creator>Luhm, Robert A.</creator><creator>Bergtrom, Gerald</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>FBQ</scope><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>7SS</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19910530</creationdate><title>Differential regulation of insect globin and actin mRNAs during larval development in Chironomus thummi</title><author>Saffarini, Daad A. ; Trewitt, Patrick M. ; Luhm, Robert A. ; Bergtrom, Gerald</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-347e091081b236998c45ddede7a5747796d7dd6f0ce0f3fba87ec07d16ceae833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>20-hydroxyecdysone</topic><topic>act gene</topic><topic>actin</topic><topic>Actins - genetics</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>biological development</topic><topic>Chironomidae</topic><topic>Chironomidae - drug effects</topic><topic>Chironomidae - genetics</topic><topic>Chironomidae - growth &amp; development</topic><topic>Chironomidae - metabolism</topic><topic>Chironomus riparius</topic><topic>Chironomus thummi thummi</topic><topic>Diptera</topic><topic>DNA, Recombinant</topic><topic>ecdysterone</topic><topic>Ecdysterone - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>gb gene</topic><topic>genbank/m57410</topic><topic>genbank/m57411</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>genetic regulation</topic><topic>globin mRNA accumulation</topic><topic>globins</topic><topic>Globins - genetics</topic><topic>Larva - metabolism</topic><topic>larvae</topic><topic>messenger RNA</topic><topic>midge</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Molecular Sequence Data</topic><topic>multigene family</topic><topic>Recombinant DNA</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>S1 nuclease protection</topic><topic>Single-Strand Specific DNA and RNA Endonucleases - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saffarini, Daad A.</creatorcontrib><creatorcontrib>Trewitt, Patrick M.</creatorcontrib><creatorcontrib>Luhm, Robert A.</creatorcontrib><creatorcontrib>Bergtrom, Gerald</creatorcontrib><collection>AGRIS</collection><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>Entomology Abstracts (Full archive)</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Gene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saffarini, Daad A.</au><au>Trewitt, Patrick M.</au><au>Luhm, Robert A.</au><au>Bergtrom, Gerald</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential regulation of insect globin and actin mRNAs during larval development in Chironomus thummi</atitle><jtitle>Gene</jtitle><addtitle>Gene</addtitle><date>1991-05-30</date><risdate>1991</risdate><volume>101</volume><issue>2</issue><spage>215</spage><epage>222</epage><pages>215-222</pages><issn>0378-1119</issn><eissn>1879-0038</eissn><coden>GENED6</coden><abstract>S1 nuclease protection assays were used to measure changes in the steady-state levels of six different globin ( Gb) mRNAs in the midge, Chironomus thummi thummi ( C. thummi, Diptera) during larval development. Two distinct patterns of change were observed. GbI, IV, VIIB-4 and VIIB-5 transcripts were present in 3rd instar larvae, rose from low levels immediately post-moult to peak levels by day 2–3 of the 4th instar, and then declined, reaching near-basal levels by day 7–8. In contrast, transcripts of GbIII (known from previous studies to be 4th instar-specific) and VI, which were undetectable in the 3rd instar, rose to high levels by day 2 of the 4th instar, but remained elevated thereafter. Our data further showed that closely linked Gb genes were not necessarily expressed in a coordinate manner. Unlike the Gb mRNAs, actin ( Act) mRNA levels (measured by slot-blot hybridization to a heterologous probe) increased progressively as a proportion of total RNA during 4th instar development. Therefore, the regulation of C. thummi Gb transcript levels is specific, differing from that of Act and among the Gb mRNAs themselves. Elevated 20-hydroxyecdysone (HE) titer at the 3rd-4th instar moult correlates with the low steady-state levels of Gb mRNAs immediately post-moult. However, other aspects of Gb mRNA profiles cannot be explained on the basis of a direct repressive effect by HE on Gb gene transcription.</abstract><cop>Lausanne</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>2055487</pmid><doi>10.1016/0378-1119(91)90414-7</doi><tpages>8</tpages></addata></record>
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identifier ISSN: 0378-1119
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source MEDLINE; Elsevier ScienceDirect Journals
subjects 20-hydroxyecdysone
act gene
actin
Actins - genetics
Amino Acid Sequence
Animals
Base Sequence
Biological and medical sciences
biological development
Chironomidae
Chironomidae - drug effects
Chironomidae - genetics
Chironomidae - growth & development
Chironomidae - metabolism
Chironomus riparius
Chironomus thummi thummi
Diptera
DNA, Recombinant
ecdysterone
Ecdysterone - pharmacology
Fundamental and applied biological sciences. Psychology
gb gene
genbank/m57410
genbank/m57411
Gene expression
Gene Expression Regulation
genetic regulation
globin mRNA accumulation
globins
Globins - genetics
Larva - metabolism
larvae
messenger RNA
midge
Molecular and cellular biology
Molecular genetics
Molecular Sequence Data
multigene family
Recombinant DNA
RNA, Messenger - genetics
RNA, Messenger - metabolism
S1 nuclease protection
Single-Strand Specific DNA and RNA Endonucleases - metabolism
title Differential regulation of insect globin and actin mRNAs during larval development in Chironomus thummi
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