Unique germ-line organelle, nuage, functions to repress selfish genetic elements in Drosophila melanogaster

被引:294
作者
Lim, Ai Khim
Kai, Toshie
机构
[1] Natl Univ Singapore, Germ Line Biol Lab, Temasek Life Sci Lab, Singapore 117604, Singapore
[2] Natl Univ Singapore, Dept Biol Sci, Singapore 117604, Singapore
基金
英国惠康基金;
关键词
Krimper; repeat-associated small interfering RNA;
D O I
10.1073/pnas.0701920104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The nuage is an electron-dense perinuclear structure that is known to be a hallmark of animal germ-line cells. Although the conservation of the nuagethroughout evolution accentuates its essentiality, its role(s) and the exact mechanism(s) by which it functions in the germ line still remain unknown. Here, we report a nuage component, Krimper (KRIMP), in Drosophila melanogaster and show that it ensures the repression of the self ish genetic elements in the female germ line. The Krimp loss-of-function allele exhibited female sterility, defects in karyosome formation and oocyte polarity, and precocious osk translation. These phenotypes are commonly observed in the other nuage component mutants, vasa (vas) and maelstrom (maen, and the RNA-silencing component mutants, spindle-E (spn-E) and aubergine (aub), suggesting a shared underlying defect that uses RNA silencing. Moreover, we demonstrated that the localization of the nuage components depends on both SPN-E and AUB and that the selfish genetic elements were derepressed to different extents in the nuage component mutants, as well as in aub and armitage (armi) mutants. In the nuage component mutants, vas, krimp, and mael, the levels of too, I-element, and HeT-A repeat-associated small interfering RNAs were greatly reduced. Hence, our data suggest that the nuage functions as a specialized center that protects the genome in the germ-line cells via gene regulation mediated by repeat-associated small interfering RNAs.
引用
收藏
页码:6714 / 6719
页数:6
相关论文
共 45 条
[1]   The small RNA profile during Drosophila melanogaster development [J].
Aravin, AA ;
Lagos-Quintana, M ;
Yalcin, A ;
Zavolan, M ;
Marks, D ;
Snyder, B ;
Gaasterland, T ;
Meyer, J ;
Tuschl, T .
DEVELOPMENTAL CELL, 2003, 5 (02) :337-350
[2]   The role of Tudor domains in germline development and polar granule architecture [J].
Arkov, Alexey L. ;
Wang, Ju-Yu S. ;
Ramos, Andres ;
Lehmann, Ruth .
DEVELOPMENT, 2006, 133 (20) :4053-4062
[3]  
BARDSLEY A, 1993, DEVELOPMENT, V119, P207
[4]   TUDOR, A GENE REQUIRED FOR ASSEMBLY OF THE GERM PLASM IN DROSOPHILA-MELANOGASTER [J].
BOSWELL, RE ;
MAHOWALD, AP .
CELL, 1985, 43 (01) :97-104
[5]   Drosophila euchromatic LTR retrotransposons are much younger than the host species in which they reside [J].
Bowen, NJ ;
McDonald, JF .
GENOME RESEARCH, 2001, 11 (09) :1527-1540
[6]   Mouse tudor repeat-1 (MTR-1) is a novel component of chromatoid bodies/nuages in male germ cells and forms a complex with snRNPs [J].
Chuma, S ;
Hiyoshi, M ;
Yamamoto, A ;
Hosokawa, M ;
Takamune, K ;
Nakatsuji, N .
MECHANISMS OF DEVELOPMENT, 2003, 120 (09) :979-990
[7]  
Clegg NJ, 1997, DEVELOPMENT, V124, P4661
[8]   The Drosophila SDE3 homolog armitage is required for oskar mRNA silencing and embryonic axis specification [J].
Cook, HA ;
Koppetsch, BS ;
Wu, J ;
Theurkauf, WE .
CELL, 2004, 116 (06) :817-829
[9]   Mouse MAELSTROM: the link between meiotic silencing of unsynapsed chromatin and microRNA pathway? [J].
Costa, Yael ;
Speed, Robert M. ;
Gautier, Philippe ;
Semple, Colin A. ;
Maratou, Klio ;
Turner, James M. A. ;
Cooke, Howard J. .
HUMAN MOLECULAR GENETICS, 2006, 15 (15) :2324-2334
[10]  
EDDY EM, 1975, INT REV CYTOL, V43, P229