TY - JOUR
T1 - Unusual expression of LINE-1 transposable element in the MRL autoimmune lymphoproliferative syndrome-prone strain
AU - Benihoud, Karim
AU - Bonardelle, Danielle
AU - Soual-Hoebeke, Emmanuelle
AU - Durand-Gasselin, Ingrid
AU - Emilie, Dominique
AU - Kiger, Nicole
AU - Bobé, Pierre
N1 - Funding Information:
We thank Pr Michel Morange (Unité de Génétique Moléculaire, Ecole Normale Supérieure, Paris, France) for the conditioning of F9 cells and Pr Marshall H. Edgell (Department of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC) for providing the sequences of L1Md-A2. We thank Dr Thierry Heidmann (Unité des Rétrovirus Endogènes et Eléments Rétroides des Eucaryotes Supérieurs, IGR/CNRS, Villejuif, France) for critical review of the manuscript. This work was supported by INSERM, CNRS and additional grants from the Association pour la Recherche sur la Polyarthrite (ARP) and Association pour la Recherche sur le Cancer (ARC grant no. 6178). K Benihoud was the recipient of an ARP fellowship.
PY - 2002/1/1
Y1 - 2002/1/1
N2 - LINE-1 are endogenous mobile genetic elements that have dispersed and accumulated in the genomes of eukaryotes via germline transposition, with up to 100000 copies in mammalian genomes. LINE-1 elements transpose by reverse transcription of their own transcript. Transposition requires synthesis of a full-length, sense-strand transcripts and proteins encoded by open reading frame (ORF) 1 and ORF2. Although severely repressed in most normal tissues, LINE-1 occasionally leads to disease by insertional mutagenesis. In the present study, Northern blot and in situ hybridization analyses revealed a template-strand transcription of LINE-1 ORF2 (encoding reverse transcriptase, RT) in lymphoid organs and the liver from MRL-+/+ and Fas-deficient MRL/lpr strains and their normal ancestors. While these sense transcripts are restricted to the nucleus in hepatocytes, they are also found in the cytoplasm in splenocytes. In contrast to transcription, ORF2 translation was detected only in MRL strains, as shown by the cytoplasmic labelling of splenic cells obtained with a monoclonal antibody recognizing the LINE-1 RT. This antibody coprecipitated two proteins of 45 and 12 kDa from MRL/lpr lymphoid organ lysates that were removed by pretreatment with anti-β2-microglobulin antiserum, suggesting a structural association between a LINE-1 product and a major histocompatibility complex class I or class I-like molecule.
AB - LINE-1 are endogenous mobile genetic elements that have dispersed and accumulated in the genomes of eukaryotes via germline transposition, with up to 100000 copies in mammalian genomes. LINE-1 elements transpose by reverse transcription of their own transcript. Transposition requires synthesis of a full-length, sense-strand transcripts and proteins encoded by open reading frame (ORF) 1 and ORF2. Although severely repressed in most normal tissues, LINE-1 occasionally leads to disease by insertional mutagenesis. In the present study, Northern blot and in situ hybridization analyses revealed a template-strand transcription of LINE-1 ORF2 (encoding reverse transcriptase, RT) in lymphoid organs and the liver from MRL-+/+ and Fas-deficient MRL/lpr strains and their normal ancestors. While these sense transcripts are restricted to the nucleus in hepatocytes, they are also found in the cytoplasm in splenocytes. In contrast to transcription, ORF2 translation was detected only in MRL strains, as shown by the cytoplasmic labelling of splenic cells obtained with a monoclonal antibody recognizing the LINE-1 RT. This antibody coprecipitated two proteins of 45 and 12 kDa from MRL/lpr lymphoid organ lysates that were removed by pretreatment with anti-β2-microglobulin antiserum, suggesting a structural association between a LINE-1 product and a major histocompatibility complex class I or class I-like molecule.
KW - Autoimmunity
KW - Endogenous retroviruses
KW - Fas
KW - LINE-1
KW - Retrotransposon
UR - http://www.scopus.com/inward/record.url?scp=0037104028&partnerID=8YFLogxK
U2 - 10.1038/sj.onc.1205730
DO - 10.1038/sj.onc.1205730
M3 - Article
C2 - 12165858
AN - SCOPUS:0037104028
SN - 0950-9232
VL - 21
SP - 5593
EP - 5600
JO - Oncogene
JF - Oncogene
IS - 36
ER -