Identification of two RNA cis-elements that function to regulate the 5′ splice site selection of Bcl-x pre-mRNA in response to ceramide

被引:52
作者
Massiello, A
Salas, A
Pinkerman, RL
Roddy, P
Roesser, JR
Chalfant, CE
机构
[1] Virginia Commonwealth Univ, Dept Biochem, Richmond, VA 23298 USA
[2] Med Univ S Carolina, Dept Biochem & Mol Biol, Charleston, SC 29425 USA
[3] Hunter Holmes McGuire Vet Affairs Med Ctr, Richmond, VA 23249 USA
[4] Massey Canc Ctr, Richmond, VA 23232 USA
关键词
D O I
10.1074/jbc.M313950200
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
Two splice variants derived from the BCL-x gene, proapoptotic Bcl-x(s) and anti-apoptotic Bcl-x(L), are produced via alternative 5' splice site selection within exon 2 of Bcl-x pre-mRNA. In previous studies, our laboratory demonstrated that ceramide regulated this 5' splice site selection, inducing the production of Bcl-x(s) mRNA with a concomitant decrease in Bcl-x(L) correlating with sensitization to chemotherapy (Chalfant, C. E., Rathman, K., Pinkerman, R. L., Wood, R. E., Obeid, L. M., Ogretmen, B., and Hannun, Y. A. (2002) J. Biol. Chem. 277, 12587-12595). We have now identified several possible RNA cis-elements within exon 2 of Bcl-x pre-mRNA by sequence analysis. To study the possible roles of these RNA cis-elements in regulating the alternative 5' splice site selection of Bcl-x pre-mRNA, we developed a BCL-x minigene construct which conferred the same ratio of Bcl-x(L)/Bcl-x(s) mRNA as the endogenous Bcl-x and was responsive to ceramide treatment. Mutagenesis of either a purine-rich splicing enhancer or a pyrimidine tract element within exon 2 induced a change in the ratio of Bcl-x(L)/Bcl-x(s) mRNA from 7 to 1 and 0.23, thereby diminishing the selection of the Bcl-x(L) 5' splice site with a concomitant increase in Bcl-x(s) 5' splice site selection. Furthermore, mutagenesis of these cis-elements abolished the ability of ceramide to affect the 5' splice site selection. In vitro binding assays coupled with competitor studies demonstrated specific binding of RNA trans-activating proteins to these regions. SDS-PAGE analysis of cross-linked RNA trans-activating factors with these RNA cis-elements revealed the binding of 215-, 120-, and 30-kDa proteins to the purine-rich element and 120- and 76-kDa proteins to the pyrimidine tract element. In addition, exogenous treatment of A549 cells with ceramide increased the formation of protein complexes with these RNA cis-elements. Therefore, we have identified two ceramide-responsive RNA cis-elements within exon 2 of Bcl-x pre-mRNA, and this is the first report of an RNA cis-element responsive to a bioactive lipid.
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页码:15799 / 15804
页数:6
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共 40 条
[21]   CROSSTALK AMONG MULTIPLE SIGNAL-ACTIVATED PHOSPHOLIPASES [J].
LISCOVITCH, M .
TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (10) :393-399
[22]   Identification of functional exonic splicing enhancer motifs recognized by individual SR proteins [J].
Liu, HX ;
Zhang, M ;
Krainer, AR .
GENES & DEVELOPMENT, 1998, 12 (13) :1998-2012
[23]   Pre-mRNA splicing in plants: Characterization of Ser Arg splicing factors [J].
Lopato, S ;
Mayeda, A ;
Krainer, AR ;
Barta, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (07) :3074-3079
[24]   SR proteins and splicing control [J].
Manley, JL ;
Tacke, R .
GENES & DEVELOPMENT, 1996, 10 (13) :1569-1579
[25]   Modification of alternative splicing of Bcl-x Pre-mRNA in prostate and breast cancer cells - Analysis of apoptosis and cell death [J].
Mercatante, DR ;
Bortner, CD ;
Cidlowski, JA ;
Kole, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (19) :16411-16417
[26]   REGULATION OF MAMMALIAN SPLICEOSOME ASSEMBLY BY A PROTEIN-PHOSPHORYLATION MECHANISM [J].
MERMOUD, JE ;
COHEN, PTW ;
LAMOND, AI .
EMBO JOURNAL, 1994, 13 (23) :5679-5688
[27]   Bcl-x(S) antagonizes the protective effects of Bcl-x(L) [J].
Minn, AJ ;
Boise, LH ;
Thompson, CB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (11) :6306-6312
[28]   Serine/threonine phosphatase 1 modulates the subnuclear distribution of pre-mRNA splicing factors [J].
Misteli, T ;
Spector, DL .
MOLECULAR BIOLOGY OF THE CELL, 1996, 7 (10) :1559-1572
[29]   PROGRAMMED CELL-DEATH INDUCED BY CERAMIDE [J].
OBEID, LM ;
LINARDIC, CM ;
KAROLAK, LA ;
HANNUN, YA .
SCIENCE, 1993, 259 (5102) :1769-1771
[30]   Biochemical mechanisms of the generation of endogenous long chain ceramide in response to exogenous short chain ceramide the A549 human lung adenocarcinoma cell line - Role for endogenous ceramide in mediating the action of exogenous ceramide [J].
Ogretmen, B ;
Pettus, BJ ;
Rossi, MJ ;
Wood, R ;
Usta, J ;
Szulc, Z ;
Bielawska, A ;
Obeid, LM ;
Hannun, YA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (15) :12960-12969