Here, we study an insect hnRNP M protein, referred to as Hrp59. Hrp59 is relatively abundant, has a modular domain organization containing three RNA-binding domains, is dynamically recruited to transcribed genes, and binds to premRNA cotranscriptionally. Using the Balbiani ring system of Chironomus, we show that Hrp59 accompanies the mRNA from the gene to the nuclear envelope, and is released from the mRNA at the nuclear pore. The association of Hrp59 with transcribed genes is not proportional to the amount of synthesized RNA, and in vivo Hrp59 binds preferentially to a subset of mRNAs, including its own mRNA. By coimmunoprecipitation of Hrp59–RNA complexes and microarray hybridization against Drosophila whole-genome arrays, we identify the preferred mRNA targets of Hrp59 in vivo and show that Hrp59 is required for the expression of these target mRNAs. We also show that Hrp59 binds preferentially to exonic splicing enhancers and our results provide new insights into the role of hnRNP M in splicing regulation.
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28 March 2005
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March 21 2005
Hrp59, an hnRNP M protein in Chironomus and Drosophila, binds to exonic splicing enhancers and is required for expression of a subset of mRNAs
Eva Kiesler,
Eva Kiesler
1Department of Molecular Biology and Functional Genomics, Stockholm University, SE-10691 Stockholm, Sweden
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Manuela E. Hase,
Manuela E. Hase
1Department of Molecular Biology and Functional Genomics, Stockholm University, SE-10691 Stockholm, Sweden
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David Brodin,
David Brodin
2Department of Biosciences at Novum, Karolinska Institute, SE-14157 Huddinge, Sweden
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Neus Visa
Neus Visa
1Department of Molecular Biology and Functional Genomics, Stockholm University, SE-10691 Stockholm, Sweden
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Eva Kiesler
1Department of Molecular Biology and Functional Genomics, Stockholm University, SE-10691 Stockholm, Sweden
Manuela E. Hase
1Department of Molecular Biology and Functional Genomics, Stockholm University, SE-10691 Stockholm, Sweden
David Brodin
2Department of Biosciences at Novum, Karolinska Institute, SE-14157 Huddinge, Sweden
Neus Visa
1Department of Molecular Biology and Functional Genomics, Stockholm University, SE-10691 Stockholm, Sweden
Correspondence to Neus Visa: [email protected]
E. Kiesler and M. Hase have contributed equally to this work.
Abbreviations used in this paper: BR, Balbiani ring; BrUTP, bromo-UTP; CAT, chloramphenicol acetyltransferase; CF, connecting fiber; DSP, dithiobis-succinimidyl propionate; ESE, exonic splicing enhancer; IP, immunoprecipitation; NPC, nuclear pore complex; premRNP, premessenger RNP complex; RRM, RNA-recognition motif.
Received:
July 27 2004
Accepted:
February 15 2005
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2005
J Cell Biol (2005) 168 (7): 1013–1025.
Article history
Received:
July 27 2004
Accepted:
February 15 2005
Citation
Eva Kiesler, Manuela E. Hase, David Brodin, Neus Visa; Hrp59, an hnRNP M protein in Chironomus and Drosophila, binds to exonic splicing enhancers and is required for expression of a subset of mRNAs . J Cell Biol 28 March 2005; 168 (7): 1013–1025. doi: https://doi.org/10.1083/jcb.200407173
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