Expression of LINE-1 retroposons is essential for murine preimplantation development

被引:116
作者
Beraldi, R
Pittoggi, C
Sciamanna, I
Mattei, E
Spadafora, C
机构
[1] Ist Super Sanita, I-00161 Rome, Italy
[2] Univ Siena, I-53100 Siena, Italy
[3] CNR, Natl Res Council, Inst Biol & Mol Pathol, Rome, Italy
关键词
developmental biology; early embryogenesis; LINE-1/L1; retrotransposon; reverse transcriptase; gene regulation;
D O I
10.1002/mrd.20423
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
In higher eukaryotes, reverse transcriptase (RT) activities are encoded by a variety of endogenous retroviruses and retrotransposable elements. We previously found that mouse preimplantation embryos are endowed with an endogenous RT activity. Inhibition of that activity by the non nucleosidic inhibitor nevirapine or by microinjection of anti-RT antibody caused early embryonic developmental arrest. Those experiments indicated that RT is required for early development, but did not identify the responsible coding elements. We now show that microinjection of morpholino-modified antisense oligonucleotides targeting the 5' end region of active LINE-1 retrotransposons in murine zygotes irreversibly arrests preimplantation development at the two- and four-cell stages; the overall level of functional RT is concomitantly downregulated in arrested embryos. Furthermore, we show that the induction of embryo developmental arrest is associated with a substantial reprogramming of gene expression. Together, these results support the conclusion that expression of LINE-1 retrotransposons is required for early embryo preimplantation development.
引用
收藏
页码:279 / 287
页数:9
相关论文
共 33 条
[1]   Hot L1s account for the bulk of retrotransposition in the human population [J].
Brouha, B ;
Schustak, J ;
Badge, RM ;
Lutz-Prigget, S ;
Farley, AH ;
Moran, JV ;
Kazazian, HH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (09) :5280-5285
[2]   Mobile elements and mammalian genome evolution [J].
Deininger, PL ;
Moran, JV ;
Batzer, MA ;
Kazazian, HH .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2003, 13 (06) :651-658
[3]   Retrotransposon-derived elements in the mammalian genome: A potential source of disease [J].
Druker, R ;
Whitelaw, E .
JOURNAL OF INHERITED METABOLIC DISEASE, 2004, 27 (03) :319-330
[4]   Systems biology of the 2-cell mouse embryo [J].
Evsikov, AV ;
de Vries, WN ;
Peaston, AE ;
Radford, EE ;
Fancher, KS ;
Chen, FH ;
Blake, JA ;
Bult, CJ ;
Latham, KE ;
Solter, D ;
Knowles, BB .
CYTOGENETIC AND GENOME RESEARCH, 2004, 105 (2-4) :240-250
[5]   Reverse transcriptase activity in mature spermatozoa of mouse [J].
Giordano, R ;
Magnano, AR ;
Zaccagnini, G ;
Pittoggi, C ;
Moscufo, N ;
Lorenzini, R ;
Spadafora, C .
JOURNAL OF CELL BIOLOGY, 2000, 148 (06) :1107-1113
[6]   Transcriptional disruption by the L1 retrotransposon and implications for mammalian transcriptomes [J].
Han, JS ;
Szak, ST ;
Boeke, JD .
NATURE, 2004, 429 (6989) :268-274
[7]   Transcriptional activation of retrotransposons alters the expression of adjacent genes in wheat [J].
Kashkush, K ;
Feldman, M ;
Levy, AA .
NATURE GENETICS, 2003, 33 (01) :102-106
[8]   MuERV-L is one of the earliest transcribed genes in mouse one-cell embryos [J].
Kigami, D ;
Minami, N ;
Takayama, H ;
Imai, H .
BIOLOGY OF REPRODUCTION, 2003, 68 (02) :651-654
[9]   Initial sequencing and analysis of the human genome [J].
Lander, ES ;
Int Human Genome Sequencing Consortium ;
Linton, LM ;
Birren, B ;
Nusbaum, C ;
Zody, MC ;
Baldwin, J ;
Devon, K ;
Dewar, K ;
Doyle, M ;
FitzHugh, W ;
Funke, R ;
Gage, D ;
Harris, K ;
Heaford, A ;
Howland, J ;
Kann, L ;
Lehoczky, J ;
LeVine, R ;
McEwan, P ;
McKernan, K ;
Meldrim, J ;
Mesirov, JP ;
Miranda, C ;
Morris, W ;
Naylor, J ;
Raymond, C ;
Rosetti, M ;
Santos, R ;
Sheridan, A ;
Sougnez, C ;
Stange-Thomann, N ;
Stojanovic, N ;
Subramanian, A ;
Wyman, D ;
Rogers, J ;
Sulston, J ;
Ainscough, R ;
Beck, S ;
Bentley, D ;
Burton, J ;
Clee, C ;
Carter, N ;
Coulson, A ;
Deadman, R ;
Deloukas, P ;
Dunham, A ;
Dunham, I ;
Durbin, R ;
French, L .
NATURE, 2001, 409 (6822) :860-921
[10]   Resistance of IAPs to methylation reprogramming may provide a mechanism for epigenetic inheritance in the mouse [J].
Lane, N ;
Dean, W ;
Erhardt, S ;
Hajkova, P ;
Surani, A ;
Walter, J ;
Reik, W .
GENESIS, 2003, 35 (02) :88-93