CACTIN is an essential nuclear protein in Arabidopsis and may be associated with the eukaryotic spliceosome

被引:27
作者
Baldwin, Katherine L. [1 ,2 ]
Dinh, Elizabeth M. [3 ]
Hart, Brian M. [3 ]
Masson, Patrick H. [1 ,2 ]
机构
[1] Univ Wisconsin, Genet Lab, Madison, WI 53706 USA
[2] Univ Wisconsin, Program Cellular & Mol Biol, Madison, WI 53706 USA
[3] Univ Wisconsin, Coll Letters & Sci, Madison, WI 53706 USA
基金
美国国家科学基金会;
关键词
Arabidopsis; CACTIN; Spliceosome; Development; AT5G63440; AT1G49170; SR SPLICING FACTORS; KAPPA-B; COLOCALIZATION; EXPRESSION; CORE; INTERACTS; DYNAMICS; ELEGANS; PLANTS; STEP;
D O I
10.1016/j.febslet.2013.02.041
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
CACTIN is a conserved eukaryotic protein without known functional domains. Previous research revealed that CACTIN is essential in animals and protists and that it may function in inflammation pathways in animals; however, these pathways are not as broadly conserved as CACTIN. Therefore, the ancestral molecular function of CACTIN remains unknown. Our studies using Arabidopsis show that CACTIN is required for embryogenesis. Fluorescently tagged CACTIN localizes to nuclear speckles and colocalizes with known splicing proteins. In yeast-two-hybrid studies, we found that CACTIN binds to a putative component of the spliceosome. These findings support a possible role for CACTIN in splicing. Structured summary of protein interactions: Cactin and SR45colocalize by fluorescence microscopy (View interaction) Cactin and RSP31colocalize by fluorescence microscopy (View interaction) Cactin and AT5G63440physically interacts withby two hybrid (View Interaction: 1, 2, 3) Cactin and AT5G63440colocalize by fluorescence microscopy (View interaction) ATG7physically interacts with ATG12A by two hybrid (View Interaction: 1, 2) (C) 2013 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:873 / 879
页数:7
相关论文
共 36 条
[1]   Quantifying Colocalization by Correlation: The Pearson Correlation Coefficient is Superior to the Mander's Overlap Coefficient [J].
Adler, Jeremy ;
Parmryd, Ingela .
CYTOMETRY PART A, 2010, 77A (08) :733-742
[2]   CHARACTERIZATION OF A NOVEL GENE IN THE HUMAN MAJOR HISTOCOMPATIBILITY COMPLEX THAT ENCODES A POTENTIAL NEW MEMBER OF THE I-KAPPA-B FAMILY OF PROTEINS [J].
ALBERTELLA, MR ;
CAMPBELL, RD .
HUMAN MOLECULAR GENETICS, 1994, 3 (05) :793-799
[3]   DIFFERENTIAL STAINING OF ABORTED AND NONABORTED POLLEN [J].
ALEXANDER, MP .
STAIN TECHNOLOGY, 1969, 44 (03) :117-+
[4]   Nuclear localization and in vivo dynamics of a plant-specific serine/arginine-rich protein [J].
Ali, GS ;
Golovkin, M ;
Reddy, ASN .
PLANT JOURNAL, 2003, 36 (06) :883-893
[5]   Regulation of Plant Developmental Processes by a Novel Splicing Factor [J].
Ali, Gul Shad ;
Palusa, Saiprasad G. ;
Golovkin, Maxim ;
Prasad, Jayendra ;
Manley, James L. ;
Reddy, Anireddy S. N. .
PLOS ONE, 2007, 2 (05)
[6]   Letter to the Editor:: Resonance assignments for the hypothetical protein yggU from Escherichia coli [J].
Aramini, JM ;
Mills, JL ;
Xiao, R ;
Acton, TB ;
Wu, MJ ;
Szyperski, T ;
Montelione, GT .
JOURNAL OF BIOMOLECULAR NMR, 2003, 27 (03) :285-286
[7]   Cactin Targets the MHC Class III Protein IκB-like (IκBL) and Inhibits NF-κB and Interferon-regulatory Factor Signaling Pathways [J].
Atzei, Paola ;
Gargan, Siobhan ;
Curran, Niamh ;
Moynagh, Paul N. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (47) :36804-36817
[8]   Characterisation of expression patterns and functional role of Cactin in early zebrafish development [J].
Atzei, Paola ;
Yang, Fan ;
Collery, Ross ;
Kennedy, Breandan N. ;
Moynagh, Paul N. .
GENE EXPRESSION PATTERNS, 2010, 10 (4-5) :199-206
[9]   Isolation of an active step I spliceosome and composition of its RNP core [J].
Bessonov, Sergey ;
Anokhina, Maria ;
Will, Cindy L. ;
Urlaub, Henning ;
Luehrmann, Reinhard .
NATURE, 2008, 452 (7189) :846-U3
[10]   A guided tour into subcellular colocalization analysis in light microscopy [J].
Bolte, S. ;
Cordelieres, F. P. .
JOURNAL OF MICROSCOPY, 2006, 224 (213-232) :213-232