Novel mRNA-containing cytoplasmic granules in ALK-transformed cells

被引:5
作者
Fawal, Mohamad [1 ]
Jean-Jean, Olivier [2 ]
Vanzo, Nathalie [1 ]
Morello, Dominique [1 ]
机构
[1] Univ Toulouse 3, CNRS, UMR 5547, IFR 109, F-31062 Toulouse, France
[2] UPMC Univ Paris 06, CNRS, FRE 3402, F-75005 Paris, France
关键词
ANAPLASTIC LYMPHOMA KINASE; STRESS GRANULES; TYROSINE KINASE; PROCESSING BODIES; POSITIVE LYMPHOMA; BINDING-PROTEIN; EXPRESSION; TRANSPORT; DISEASE; SITES;
D O I
10.1091/mbc.E10-07-0569
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In mammalian cells, nontranslating messenger RNAs (mRNAs) are concentrated in different cytoplasmic foci, such as processing bodies (PBs) and stress granules (SGs), where they are either degraded or stored. In the present study, we have thoroughly characterized cytoplasmic foci, hereafter called AGs for ALK granules that form in transformed cells expressing the constitutively active anaplastic lymphoma kinase (ALK). AGs contain polyadenylated mRNAs and a unique combination of several RNA binding proteins that so far has not been described in mammalian foci, including AUF1, HuR, and the poly (A(+)) binding protein PABP. AGs shelter neither components of the mRNA degradation machinery present in PBs nor known markers of SGs, such as translation initiation factors or TIA/TIAR, showing that they are distinct from PBs or SGs. AGs and PBs, however, both move on microtubules with similar dynamics and frequently establish close contacts. In addition, in conditions in which mRNA metabolism is perturbed, AGs concentrate PB components with the noticeable exception of the 5' to 3' exonuclease XRN1. Altogether, we show that AGs constitute novel mRNA-containing cytoplasmic foci and we propose that they could protect translatable mRNAs from degradation, contributing thus to ALK-mediated oncogenicity.
引用
收藏
页码:726 / 735
页数:10
相关论文
共 50 条
[1]   The Dynamics of Mammalian P Body Transport, Assembly, and Disassembly In Vivo [J].
Aizer, Adva ;
Brody, Yehuda ;
Ler, Lian Wee ;
Sonenberg, Nahum ;
Singer, Robert H. ;
Shav-Tal, Yaron .
MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (10) :4154-4166
[2]   Stress granules: The Tao of RNA triage [J].
Anderson, Paul ;
Kedersha, Nancy .
TRENDS IN BIOCHEMICAL SCIENCES, 2008, 33 (03) :141-150
[3]   RNA granules: post-transcriptional and epigenetic modulators of gene expression [J].
Anderson, Paul ;
Kedersha, Nancy .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (06) :430-436
[4]   Differential effects of X-ALK fusion proteins on proliferation, transformation, and invasion properties of NIH3T3 cells [J].
Armstrong, F ;
Duplantier, MM ;
Trempat, P ;
Hieblot, C ;
Lamant, L ;
Espinos, E ;
Racaud-Sultan, C ;
Allouche, M ;
Campo, E ;
Delsol, G ;
Touriol, C .
ONCOGENE, 2004, 23 (36) :6071-6082
[5]   Nucleophosmin-anaplastic lymphoma kinase associated with anaplastic large-cell lymphoma activates the phosphatidylinositol 3-kinase/Akt antiapoptotic signaling pathway [J].
Bai, RY ;
Tao, OY ;
Miething, C ;
Morris, SW ;
Peschel, C ;
Duyster, J .
BLOOD, 2000, 96 (13) :4319-4327
[6]   Polysomes, P bodies and stress granules: states and fates of eukaryotic mRNAs [J].
Balagopal, Vidya ;
Parker, Roy .
CURRENT OPINION IN CELL BIOLOGY, 2009, 21 (03) :403-408
[7]   ALK-positive lymphoma:: A single disease with a broad spectrum of morphology [J].
Benharroch, D ;
Meguerian-Bedoyan, Z ;
Lamant, L ;
Amin, C ;
Brugières, L ;
Terrier-Lacombe, MJ ;
Haralambieva, E ;
Pulford, K ;
Pileri, S ;
Morris, SW ;
Mason, DY ;
Delsol, G .
BLOOD, 1998, 91 (06) :2076-2084
[8]   Post-transcriptional regulation of gene expression by degradation of messenger RNAs [J].
Bevilacqua, A ;
Ceriani, MC ;
Capaccioli, S ;
Nicolin, A .
JOURNAL OF CELLULAR PHYSIOLOGY, 2003, 195 (03) :356-372
[9]   Stress-induced reversal of microRNA repression and mRNA P-body localization in human cells [J].
Bhattacharyya, S. N. ;
Habermacher, R. ;
Martine, U. ;
Closs, E. I. ;
Filipowicz, W. .
COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 2006, 71 :513-521
[10]   Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies [J].
Brengues, M ;
Teixeira, D ;
Parker, R .
SCIENCE, 2005, 310 (5747) :486-489