Loading…
The Overgrown Hematopoietic Organs-31 Tumor Suppressor Gene of Drosophila Encodes an Importin-Like Protein Accumulating in the Nucleus at the Onset of Mitosis
The tumor suppressor gene overgrown hematopoietic organs- 31 (oho31) of Drosophila encodes a protein with extensive homology to the Importin protein of Xenopus (50% identity), the related yeast SRP1 protein, and the mammalian hSRP1 and RCH1 proteins. A strong reduction in the expression of oho31 by...
Saved in:
Published in: | The Journal of cell biology 1995-06, Vol.129 (6), p.1473-1489 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c530t-546d2778ffd70f0a6de4036b4c99b19da5b0137add23141210274d4fe8737c393 |
---|---|
cites | |
container_end_page | 1489 |
container_issue | 6 |
container_start_page | 1473 |
container_title | The Journal of cell biology |
container_volume | 129 |
creator | Török, Istvan Strand, Dennis Schmitt, Rolf Tick, Gabriella Török, Tibor Kiss, Istvan Mechler, Bernard M. |
description | The tumor suppressor gene overgrown hematopoietic organs- 31 (oho31) of Drosophila encodes a protein with extensive homology to the Importin protein of Xenopus (50% identity), the related yeast SRP1 protein, and the mammalian hSRP1 and RCH1 proteins. A strong reduction in the expression of oho31 by a P element inserted in the 5′ untranslated region of the oho31 transcript or a complete inactivation of oho31 by imprecise P element excision leads to malignant development of the hematopoietic organs and the genital disc, as shown by their growth autonomy in transplantation assays. We have cloned the oho31 gene of Drosophila melanogaster and determined its nucleotide sequence. The gene encodes a phosphoprotein of 522 amino acids made of three domains: a central hydrophobic domain of eight repeats of 42-44 amino acids each, displaying similarity to the arm motif found in junctional and nucleopore complex proteins, and flanked by two hydrophilic NH2- and COOH-terminal domains. Immunostaining revealed that the OHO31 protein is supplied maternally and rapidly degraded during the first 13 nuclear divisions. Thereafter, the OHO31 protein is predominantly expressed, albeit at reduced levels, in proliferating tissues. During the interphase of early embryonic cell cycles, the OHO31 protein is present in the cytoplasm and massively accumulates in the nucleus at the onset of mitosis in late interphase and prophase. The nuclear import of OHO31 is, however, less pronounced during later developmental stages. These results suggest that, similar to Importin, OHO31 may act as a cytosolic factor in nuclear transport. Moreover, the cell cycle-dependent accumulation of OHO31 in the nucleus indicates that this protein may be required for critical nuclear reactions occurring at the onset of mitosis. |
doi_str_mv | 10.1083/jcb.129.6.1473 |
format | article |
fullrecord | <record><control><sourceid>jstor_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2291178</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>1616924</jstor_id><sourcerecordid>1616924</sourcerecordid><originalsourceid>FETCH-LOGICAL-c530t-546d2778ffd70f0a6de4036b4c99b19da5b0137add23141210274d4fe8737c393</originalsourceid><addsrcrecordid>eNpdkUuP0zAUhSMEGsrAlhVIFgt2CX4ljjdIo2GYGalQJMracp2b1iWxg-0M4s_wW3FpNTxW9tU597vXPkXxnOCK4Ja92ZtNRaismopwwR4UC1JzXLaE44fFAmNKSlnT-nHxJMY9xpgLzs6KMyEkZlwuip_rHaDVHYRt8N8duoFRJz95C8katApb7WLJCFrPow_o8zxNAWLM12twgHyP3gUf_bSzg0ZXzvgOItIO3Y6TD8m6cmm_AvoUfALr0IUx8zgPOgtblOuUR3-czQBzbkq_y5WLkA7cDzb5aOPT4lGvhwjPTud58eX91fryplyurm8vL5alqRlOZc2bjgrR9n0ncI910wHHrNlwI-WGyE7XG0yY0F1HGeGEEkwF73gPrWDCMMnOi7dH7jRvRugMuBT0oKZgRx1-KK-t-ldxdqe2_k5RKgkRbQa8PgGC_zZDTGq00cAwaAd-joo0rcACH4yv_jPu_RxcfpyiRGApZUOzqTqaTP7eGKC_34RgdYhd5dhVjl016hB7bnj59_739lPOWX9x1Pcx-fCH1pBGUs5-AWeItIU</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>217099962</pqid></control><display><type>article</type><title>The Overgrown Hematopoietic Organs-31 Tumor Suppressor Gene of Drosophila Encodes an Importin-Like Protein Accumulating in the Nucleus at the Onset of Mitosis</title><source>Alma/SFX Local Collection</source><creator>Török, Istvan ; Strand, Dennis ; Schmitt, Rolf ; Tick, Gabriella ; Török, Tibor ; Kiss, Istvan ; Mechler, Bernard M.</creator><creatorcontrib>Török, Istvan ; Strand, Dennis ; Schmitt, Rolf ; Tick, Gabriella ; Török, Tibor ; Kiss, Istvan ; Mechler, Bernard M.</creatorcontrib><description>The tumor suppressor gene overgrown hematopoietic organs- 31 (oho31) of Drosophila encodes a protein with extensive homology to the Importin protein of Xenopus (50% identity), the related yeast SRP1 protein, and the mammalian hSRP1 and RCH1 proteins. A strong reduction in the expression of oho31 by a P element inserted in the 5′ untranslated region of the oho31 transcript or a complete inactivation of oho31 by imprecise P element excision leads to malignant development of the hematopoietic organs and the genital disc, as shown by their growth autonomy in transplantation assays. We have cloned the oho31 gene of Drosophila melanogaster and determined its nucleotide sequence. The gene encodes a phosphoprotein of 522 amino acids made of three domains: a central hydrophobic domain of eight repeats of 42-44 amino acids each, displaying similarity to the arm motif found in junctional and nucleopore complex proteins, and flanked by two hydrophilic NH2- and COOH-terminal domains. Immunostaining revealed that the OHO31 protein is supplied maternally and rapidly degraded during the first 13 nuclear divisions. Thereafter, the OHO31 protein is predominantly expressed, albeit at reduced levels, in proliferating tissues. During the interphase of early embryonic cell cycles, the OHO31 protein is present in the cytoplasm and massively accumulates in the nucleus at the onset of mitosis in late interphase and prophase. The nuclear import of OHO31 is, however, less pronounced during later developmental stages. These results suggest that, similar to Importin, OHO31 may act as a cytosolic factor in nuclear transport. Moreover, the cell cycle-dependent accumulation of OHO31 in the nucleus indicates that this protein may be required for critical nuclear reactions occurring at the onset of mitosis.</description><identifier>ISSN: 0021-9525</identifier><identifier>EISSN: 1540-8140</identifier><identifier>DOI: 10.1083/jcb.129.6.1473</identifier><identifier>PMID: 7790349</identifier><identifier>CODEN: JCLBA3</identifier><language>eng</language><publisher>United States: Rockefeller University Press</publisher><subject>alpha Karyopherins ; Amino Acid Sequence ; Animals ; Antibodies ; Base Sequence ; Blotting, Western ; Cell Cycle ; Cell Nucleus - metabolism ; Cell Nucleus - ultrastructure ; Cells ; Cellular biology ; Drosophila ; Drosophila melanogaster - embryology ; Drosophila melanogaster - genetics ; Drosophila melanogaster - growth & development ; Drosophila Proteins ; Embryo, Nonmammalian - physiology ; Embryonic and Fetal Development ; Embryos ; Gene Expression ; Genes ; Genes, Tumor Suppressor ; Genetic mutation ; Genetics ; Immunity (Disease) ; In Situ Hybridization ; Insect larvae ; Insects ; Karyopherins ; Larvae ; Larval development ; Mammals ; Mitosis ; Molecular Sequence Data ; Mutagenesis, Insertional ; Nuclear Proteins - biosynthesis ; Nuclear Proteins - genetics ; Phosphoproteins - biosynthesis ; Phosphoproteins - genetics ; Restriction Mapping ; Saccharomyces cerevisiae ; Saccharomyces cerevisiae - genetics ; Sequence Homology, Amino Acid ; Transcription, Genetic ; Transposons ; Tumors ; Xenopus</subject><ispartof>The Journal of cell biology, 1995-06, Vol.129 (6), p.1473-1489</ispartof><rights>Copyright 1995 The Rockefeller University Press</rights><rights>Copyright Rockefeller University Press Jun 1995</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c530t-546d2778ffd70f0a6de4036b4c99b19da5b0137add23141210274d4fe8737c393</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7790349$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Török, Istvan</creatorcontrib><creatorcontrib>Strand, Dennis</creatorcontrib><creatorcontrib>Schmitt, Rolf</creatorcontrib><creatorcontrib>Tick, Gabriella</creatorcontrib><creatorcontrib>Török, Tibor</creatorcontrib><creatorcontrib>Kiss, Istvan</creatorcontrib><creatorcontrib>Mechler, Bernard M.</creatorcontrib><title>The Overgrown Hematopoietic Organs-31 Tumor Suppressor Gene of Drosophila Encodes an Importin-Like Protein Accumulating in the Nucleus at the Onset of Mitosis</title><title>The Journal of cell biology</title><addtitle>J Cell Biol</addtitle><description>The tumor suppressor gene overgrown hematopoietic organs- 31 (oho31) of Drosophila encodes a protein with extensive homology to the Importin protein of Xenopus (50% identity), the related yeast SRP1 protein, and the mammalian hSRP1 and RCH1 proteins. A strong reduction in the expression of oho31 by a P element inserted in the 5′ untranslated region of the oho31 transcript or a complete inactivation of oho31 by imprecise P element excision leads to malignant development of the hematopoietic organs and the genital disc, as shown by their growth autonomy in transplantation assays. We have cloned the oho31 gene of Drosophila melanogaster and determined its nucleotide sequence. The gene encodes a phosphoprotein of 522 amino acids made of three domains: a central hydrophobic domain of eight repeats of 42-44 amino acids each, displaying similarity to the arm motif found in junctional and nucleopore complex proteins, and flanked by two hydrophilic NH2- and COOH-terminal domains. Immunostaining revealed that the OHO31 protein is supplied maternally and rapidly degraded during the first 13 nuclear divisions. Thereafter, the OHO31 protein is predominantly expressed, albeit at reduced levels, in proliferating tissues. During the interphase of early embryonic cell cycles, the OHO31 protein is present in the cytoplasm and massively accumulates in the nucleus at the onset of mitosis in late interphase and prophase. The nuclear import of OHO31 is, however, less pronounced during later developmental stages. These results suggest that, similar to Importin, OHO31 may act as a cytosolic factor in nuclear transport. Moreover, the cell cycle-dependent accumulation of OHO31 in the nucleus indicates that this protein may be required for critical nuclear reactions occurring at the onset of mitosis.</description><subject>alpha Karyopherins</subject><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Base Sequence</subject><subject>Blotting, Western</subject><subject>Cell Cycle</subject><subject>Cell Nucleus - metabolism</subject><subject>Cell Nucleus - ultrastructure</subject><subject>Cells</subject><subject>Cellular biology</subject><subject>Drosophila</subject><subject>Drosophila melanogaster - embryology</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila melanogaster - growth & development</subject><subject>Drosophila Proteins</subject><subject>Embryo, Nonmammalian - physiology</subject><subject>Embryonic and Fetal Development</subject><subject>Embryos</subject><subject>Gene Expression</subject><subject>Genes</subject><subject>Genes, Tumor Suppressor</subject><subject>Genetic mutation</subject><subject>Genetics</subject><subject>Immunity (Disease)</subject><subject>In Situ Hybridization</subject><subject>Insect larvae</subject><subject>Insects</subject><subject>Karyopherins</subject><subject>Larvae</subject><subject>Larval development</subject><subject>Mammals</subject><subject>Mitosis</subject><subject>Molecular Sequence Data</subject><subject>Mutagenesis, Insertional</subject><subject>Nuclear Proteins - biosynthesis</subject><subject>Nuclear Proteins - genetics</subject><subject>Phosphoproteins - biosynthesis</subject><subject>Phosphoproteins - genetics</subject><subject>Restriction Mapping</subject><subject>Saccharomyces cerevisiae</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Sequence Homology, Amino Acid</subject><subject>Transcription, Genetic</subject><subject>Transposons</subject><subject>Tumors</subject><subject>Xenopus</subject><issn>0021-9525</issn><issn>1540-8140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNpdkUuP0zAUhSMEGsrAlhVIFgt2CX4ljjdIo2GYGalQJMracp2b1iWxg-0M4s_wW3FpNTxW9tU597vXPkXxnOCK4Ja92ZtNRaismopwwR4UC1JzXLaE44fFAmNKSlnT-nHxJMY9xpgLzs6KMyEkZlwuip_rHaDVHYRt8N8duoFRJz95C8katApb7WLJCFrPow_o8zxNAWLM12twgHyP3gUf_bSzg0ZXzvgOItIO3Y6TD8m6cmm_AvoUfALr0IUx8zgPOgtblOuUR3-czQBzbkq_y5WLkA7cDzb5aOPT4lGvhwjPTud58eX91fryplyurm8vL5alqRlOZc2bjgrR9n0ncI910wHHrNlwI-WGyE7XG0yY0F1HGeGEEkwF73gPrWDCMMnOi7dH7jRvRugMuBT0oKZgRx1-KK-t-ldxdqe2_k5RKgkRbQa8PgGC_zZDTGq00cAwaAd-joo0rcACH4yv_jPu_RxcfpyiRGApZUOzqTqaTP7eGKC_34RgdYhd5dhVjl016hB7bnj59_739lPOWX9x1Pcx-fCH1pBGUs5-AWeItIU</recordid><startdate>19950601</startdate><enddate>19950601</enddate><creator>Török, Istvan</creator><creator>Strand, Dennis</creator><creator>Schmitt, Rolf</creator><creator>Tick, Gabriella</creator><creator>Török, Tibor</creator><creator>Kiss, Istvan</creator><creator>Mechler, Bernard M.</creator><general>Rockefeller University Press</general><general>The Rockefeller University Press</general><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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7SS</scope><scope>5PM</scope></search><sort><creationdate>19950601</creationdate><title>The Overgrown Hematopoietic Organs-31 Tumor Suppressor Gene of Drosophila Encodes an Importin-Like Protein Accumulating in the Nucleus at the Onset of Mitosis</title><author>Török, Istvan ; Strand, Dennis ; Schmitt, Rolf ; Tick, Gabriella ; Török, Tibor ; Kiss, Istvan ; Mechler, Bernard M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c530t-546d2778ffd70f0a6de4036b4c99b19da5b0137add23141210274d4fe8737c393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>alpha Karyopherins</topic><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Base Sequence</topic><topic>Blotting, Western</topic><topic>Cell Cycle</topic><topic>Cell Nucleus - metabolism</topic><topic>Cell Nucleus - ultrastructure</topic><topic>Cells</topic><topic>Cellular biology</topic><topic>Drosophila</topic><topic>Drosophila melanogaster - embryology</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila melanogaster - growth & development</topic><topic>Drosophila Proteins</topic><topic>Embryo, Nonmammalian - physiology</topic><topic>Embryonic and Fetal Development</topic><topic>Embryos</topic><topic>Gene Expression</topic><topic>Genes</topic><topic>Genes, Tumor Suppressor</topic><topic>Genetic mutation</topic><topic>Genetics</topic><topic>Immunity (Disease)</topic><topic>In Situ Hybridization</topic><topic>Insect larvae</topic><topic>Insects</topic><topic>Karyopherins</topic><topic>Larvae</topic><topic>Larval development</topic><topic>Mammals</topic><topic>Mitosis</topic><topic>Molecular Sequence Data</topic><topic>Mutagenesis, Insertional</topic><topic>Nuclear Proteins - biosynthesis</topic><topic>Nuclear Proteins - genetics</topic><topic>Phosphoproteins - biosynthesis</topic><topic>Phosphoproteins - genetics</topic><topic>Restriction Mapping</topic><topic>Saccharomyces cerevisiae</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Sequence Homology, Amino Acid</topic><topic>Transcription, Genetic</topic><topic>Transposons</topic><topic>Tumors</topic><topic>Xenopus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Török, Istvan</creatorcontrib><creatorcontrib>Strand, Dennis</creatorcontrib><creatorcontrib>Schmitt, Rolf</creatorcontrib><creatorcontrib>Tick, Gabriella</creatorcontrib><creatorcontrib>Török, Tibor</creatorcontrib><creatorcontrib>Kiss, Istvan</creatorcontrib><creatorcontrib>Mechler, Bernard M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Török, Istvan</au><au>Strand, Dennis</au><au>Schmitt, Rolf</au><au>Tick, Gabriella</au><au>Török, Tibor</au><au>Kiss, Istvan</au><au>Mechler, Bernard M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Overgrown Hematopoietic Organs-31 Tumor Suppressor Gene of Drosophila Encodes an Importin-Like Protein Accumulating in the Nucleus at the Onset of Mitosis</atitle><jtitle>The Journal of cell biology</jtitle><addtitle>J Cell Biol</addtitle><date>1995-06-01</date><risdate>1995</risdate><volume>129</volume><issue>6</issue><spage>1473</spage><epage>1489</epage><pages>1473-1489</pages><issn>0021-9525</issn><eissn>1540-8140</eissn><coden>JCLBA3</coden><abstract>The tumor suppressor gene overgrown hematopoietic organs- 31 (oho31) of Drosophila encodes a protein with extensive homology to the Importin protein of Xenopus (50% identity), the related yeast SRP1 protein, and the mammalian hSRP1 and RCH1 proteins. A strong reduction in the expression of oho31 by a P element inserted in the 5′ untranslated region of the oho31 transcript or a complete inactivation of oho31 by imprecise P element excision leads to malignant development of the hematopoietic organs and the genital disc, as shown by their growth autonomy in transplantation assays. We have cloned the oho31 gene of Drosophila melanogaster and determined its nucleotide sequence. The gene encodes a phosphoprotein of 522 amino acids made of three domains: a central hydrophobic domain of eight repeats of 42-44 amino acids each, displaying similarity to the arm motif found in junctional and nucleopore complex proteins, and flanked by two hydrophilic NH2- and COOH-terminal domains. Immunostaining revealed that the OHO31 protein is supplied maternally and rapidly degraded during the first 13 nuclear divisions. Thereafter, the OHO31 protein is predominantly expressed, albeit at reduced levels, in proliferating tissues. During the interphase of early embryonic cell cycles, the OHO31 protein is present in the cytoplasm and massively accumulates in the nucleus at the onset of mitosis in late interphase and prophase. The nuclear import of OHO31 is, however, less pronounced during later developmental stages. These results suggest that, similar to Importin, OHO31 may act as a cytosolic factor in nuclear transport. Moreover, the cell cycle-dependent accumulation of OHO31 in the nucleus indicates that this protein may be required for critical nuclear reactions occurring at the onset of mitosis.</abstract><cop>United States</cop><pub>Rockefeller University Press</pub><pmid>7790349</pmid><doi>10.1083/jcb.129.6.1473</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9525 |
ispartof | The Journal of cell biology, 1995-06, Vol.129 (6), p.1473-1489 |
issn | 0021-9525 1540-8140 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2291178 |
source | Alma/SFX Local Collection |
subjects | alpha Karyopherins Amino Acid Sequence Animals Antibodies Base Sequence Blotting, Western Cell Cycle Cell Nucleus - metabolism Cell Nucleus - ultrastructure Cells Cellular biology Drosophila Drosophila melanogaster - embryology Drosophila melanogaster - genetics Drosophila melanogaster - growth & development Drosophila Proteins Embryo, Nonmammalian - physiology Embryonic and Fetal Development Embryos Gene Expression Genes Genes, Tumor Suppressor Genetic mutation Genetics Immunity (Disease) In Situ Hybridization Insect larvae Insects Karyopherins Larvae Larval development Mammals Mitosis Molecular Sequence Data Mutagenesis, Insertional Nuclear Proteins - biosynthesis Nuclear Proteins - genetics Phosphoproteins - biosynthesis Phosphoproteins - genetics Restriction Mapping Saccharomyces cerevisiae Saccharomyces cerevisiae - genetics Sequence Homology, Amino Acid Transcription, Genetic Transposons Tumors Xenopus |
title | The Overgrown Hematopoietic Organs-31 Tumor Suppressor Gene of Drosophila Encodes an Importin-Like Protein Accumulating in the Nucleus at the Onset of Mitosis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T15%3A58%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Overgrown%20Hematopoietic%20Organs-31%20Tumor%20Suppressor%20Gene%20of%20Drosophila%20Encodes%20an%20Importin-Like%20Protein%20Accumulating%20in%20the%20Nucleus%20at%20the%20Onset%20of%20Mitosis&rft.jtitle=The%20Journal%20of%20cell%20biology&rft.au=T%C3%B6r%C3%B6k,%20Istvan&rft.date=1995-06-01&rft.volume=129&rft.issue=6&rft.spage=1473&rft.epage=1489&rft.pages=1473-1489&rft.issn=0021-9525&rft.eissn=1540-8140&rft.coden=JCLBA3&rft_id=info:doi/10.1083/jcb.129.6.1473&rft_dat=%3Cjstor_pubme%3E1616924%3C/jstor_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c530t-546d2778ffd70f0a6de4036b4c99b19da5b0137add23141210274d4fe8737c393%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=217099962&rft_id=info:pmid/7790349&rft_jstor_id=1616924&rfr_iscdi=true |