Structural homology of the product of the Drosophila Krüppel gene with Xenopus transcription factor IIIA
Segmentation of the Drosophila embryo is established at around the blastoderm stage 1–3 and requires both maternal information in the egg cytoplasm 4,5 and expression of the zygotic genome. Zygotic genes involved in segmentation have been defined by mutations that affect the segmentai pattern of the...
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Veröffentlicht in: | Nature (London) 1986-01, Vol.319 (6051), p.336-339 |
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creator | Rosenberg, Urs B. Schröder, Christian Preiss, Anette Kienlin, Andrea Côté, Serge Riede, Isolde Jäckle, Herbert |
description | Segmentation of the
Drosophila
embryo is established at around the blastoderm stage
1–3
and requires both maternal information in the egg cytoplasm
4,5
and expression of the zygotic genome. Zygotic genes involved in segmentation have been defined by mutations that affect the segmentai pattern of the embryo
6–10
, and these fall into several different classes, such as the 'gap' genes, mutations of which cause the loss of contiguous segments
6
.
Krüppel
(K
r
) is an example of a
Drosophila
gap genes, strong K
r
mutant embryos lacking all thoracic and five anterior abdominal segments, with part of the remaining posterior abdominal segments being present as a mirror-image duplication (weaker alleles cause shorter deletions
11,12
). K
r
has been cloned
12
and shown to encode a blas-toderm-gastrulation stage-specific transcript expressed in regions of the embryo affected by K
r
mutants
13
. We report here that the protein product of the K
r
gene predicted from DNA sequences is structurally homologous to the transcription factor TFIIIA which regulates 5S gene expression in
Xenopus
. Like TFIIIA, the predicted K
r
protein has an internally repetitious sequence, and as has been suggested for TFIIIA, the repeat units may form DNA-binding domains. |
doi_str_mv | 10.1038/319336a0 |
format | Article |
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Drosophila
embryo is established at around the blastoderm stage
1–3
and requires both maternal information in the egg cytoplasm
4,5
and expression of the zygotic genome. Zygotic genes involved in segmentation have been defined by mutations that affect the segmentai pattern of the embryo
6–10
, and these fall into several different classes, such as the 'gap' genes, mutations of which cause the loss of contiguous segments
6
.
Krüppel
(K
r
) is an example of a
Drosophila
gap genes, strong K
r
mutant embryos lacking all thoracic and five anterior abdominal segments, with part of the remaining posterior abdominal segments being present as a mirror-image duplication (weaker alleles cause shorter deletions
11,12
). K
r
has been cloned
12
and shown to encode a blas-toderm-gastrulation stage-specific transcript expressed in regions of the embryo affected by K
r
mutants
13
. We report here that the protein product of the K
r
gene predicted from DNA sequences is structurally homologous to the transcription factor TFIIIA which regulates 5S gene expression in
Xenopus
. Like TFIIIA, the predicted K
r
protein has an internally repetitious sequence, and as has been suggested for TFIIIA, the repeat units may form DNA-binding domains.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/319336a0</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Biological and medical sciences ; Fundamental and applied biological sciences. Psychology ; Genes. Genome ; Humanities and Social Sciences ; letter ; Molecular and cellular biology ; Molecular genetics ; multidisciplinary ; Science ; Science (multidisciplinary)</subject><ispartof>Nature (London), 1986-01, Vol.319 (6051), p.336-339</ispartof><rights>Springer Nature Limited 1986</rights><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c288t-e12a01b8a828dcd6a6fa647fd853ce4e994e7a69eda92c8ddf08fb1e7453565a3</citedby><cites>FETCH-LOGICAL-c288t-e12a01b8a828dcd6a6fa647fd853ce4e994e7a69eda92c8ddf08fb1e7453565a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/319336a0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/319336a0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7874177$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Rosenberg, Urs B.</creatorcontrib><creatorcontrib>Schröder, Christian</creatorcontrib><creatorcontrib>Preiss, Anette</creatorcontrib><creatorcontrib>Kienlin, Andrea</creatorcontrib><creatorcontrib>Côté, Serge</creatorcontrib><creatorcontrib>Riede, Isolde</creatorcontrib><creatorcontrib>Jäckle, Herbert</creatorcontrib><title>Structural homology of the product of the Drosophila Krüppel gene with Xenopus transcription factor IIIA</title><title>Nature (London)</title><addtitle>Nature</addtitle><description>Segmentation of the
Drosophila
embryo is established at around the blastoderm stage
1–3
and requires both maternal information in the egg cytoplasm
4,5
and expression of the zygotic genome. Zygotic genes involved in segmentation have been defined by mutations that affect the segmentai pattern of the embryo
6–10
, and these fall into several different classes, such as the 'gap' genes, mutations of which cause the loss of contiguous segments
6
.
Krüppel
(K
r
) is an example of a
Drosophila
gap genes, strong K
r
mutant embryos lacking all thoracic and five anterior abdominal segments, with part of the remaining posterior abdominal segments being present as a mirror-image duplication (weaker alleles cause shorter deletions
11,12
). K
r
has been cloned
12
and shown to encode a blas-toderm-gastrulation stage-specific transcript expressed in regions of the embryo affected by K
r
mutants
13
. We report here that the protein product of the K
r
gene predicted from DNA sequences is structurally homologous to the transcription factor TFIIIA which regulates 5S gene expression in
Xenopus
. Like TFIIIA, the predicted K
r
protein has an internally repetitious sequence, and as has been suggested for TFIIIA, the repeat units may form DNA-binding domains.</description><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes. Genome</subject><subject>Humanities and Social Sciences</subject><subject>letter</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>multidisciplinary</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><recordid>eNplkM1KxDAUhYMoOI6Cj5CFC11UkzZN0uUw_hUHXKjgrtxJk2mHThOSFJl3c-eLWRnHjavL4Xwczj0InVNyTUkmbzJaZBkHcoAmlAmeMC7FIZoQksqEyIwfo5MQ1oSQnAo2Qe1L9IOKg4cON3ZjO7vaYmtwbDR23tajt5e33gbrmrYD_OS_Pp3THV7pXuOPNjb4XffWDQFHD31QvnWxtT02oKL1uCzL2Sk6MtAFffZ7p-jt_u51_pgsnh_K-WyRqFTKmGiaAqFLCTKVtao5cAOcCVPLPFOa6aJgWgAvdA1FqmRdGyLNkmrB8iznOWRTdLnLVWPf4LWpnG834LcVJdXPRNV-ohG92KEOgoLOjNVVG_54IQWjQozY1Q4Lo9OvtK_WdvD9-MT_yG9mlXWf</recordid><startdate>19860123</startdate><enddate>19860123</enddate><creator>Rosenberg, Urs B.</creator><creator>Schröder, Christian</creator><creator>Preiss, Anette</creator><creator>Kienlin, Andrea</creator><creator>Côté, Serge</creator><creator>Riede, Isolde</creator><creator>Jäckle, Herbert</creator><general>Nature Publishing Group UK</general><general>Nature Publishing</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19860123</creationdate><title>Structural homology of the product of the Drosophila Krüppel gene with Xenopus transcription factor IIIA</title><author>Rosenberg, Urs B. ; Schröder, Christian ; Preiss, Anette ; Kienlin, Andrea ; Côté, Serge ; Riede, Isolde ; Jäckle, Herbert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c288t-e12a01b8a828dcd6a6fa647fd853ce4e994e7a69eda92c8ddf08fb1e7453565a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Biological and medical sciences</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes. Genome</topic><topic>Humanities and Social Sciences</topic><topic>letter</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>multidisciplinary</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rosenberg, Urs B.</creatorcontrib><creatorcontrib>Schröder, Christian</creatorcontrib><creatorcontrib>Preiss, Anette</creatorcontrib><creatorcontrib>Kienlin, Andrea</creatorcontrib><creatorcontrib>Côté, Serge</creatorcontrib><creatorcontrib>Riede, Isolde</creatorcontrib><creatorcontrib>Jäckle, Herbert</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rosenberg, Urs B.</au><au>Schröder, Christian</au><au>Preiss, Anette</au><au>Kienlin, Andrea</au><au>Côté, Serge</au><au>Riede, Isolde</au><au>Jäckle, Herbert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural homology of the product of the Drosophila Krüppel gene with Xenopus transcription factor IIIA</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><date>1986-01-23</date><risdate>1986</risdate><volume>319</volume><issue>6051</issue><spage>336</spage><epage>339</epage><pages>336-339</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><coden>NATUAS</coden><abstract>Segmentation of the
Drosophila
embryo is established at around the blastoderm stage
1–3
and requires both maternal information in the egg cytoplasm
4,5
and expression of the zygotic genome. Zygotic genes involved in segmentation have been defined by mutations that affect the segmentai pattern of the embryo
6–10
, and these fall into several different classes, such as the 'gap' genes, mutations of which cause the loss of contiguous segments
6
.
Krüppel
(K
r
) is an example of a
Drosophila
gap genes, strong K
r
mutant embryos lacking all thoracic and five anterior abdominal segments, with part of the remaining posterior abdominal segments being present as a mirror-image duplication (weaker alleles cause shorter deletions
11,12
). K
r
has been cloned
12
and shown to encode a blas-toderm-gastrulation stage-specific transcript expressed in regions of the embryo affected by K
r
mutants
13
. We report here that the protein product of the K
r
gene predicted from DNA sequences is structurally homologous to the transcription factor TFIIIA which regulates 5S gene expression in
Xenopus
. Like TFIIIA, the predicted K
r
protein has an internally repetitious sequence, and as has been suggested for TFIIIA, the repeat units may form DNA-binding domains.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><doi>10.1038/319336a0</doi><tpages>4</tpages></addata></record> |
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language | eng |
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source | Nature; SpringerLink Journals - AutoHoldings |
subjects | Biological and medical sciences Fundamental and applied biological sciences. Psychology Genes. Genome Humanities and Social Sciences letter Molecular and cellular biology Molecular genetics multidisciplinary Science Science (multidisciplinary) |
title | Structural homology of the product of the Drosophila Krüppel gene with Xenopus transcription factor IIIA |
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