Telomeric position effect in Drosophila melanogaster reflects a telomere length control mechanism

被引:16
作者
Mason, JM [1 ]
Konev, AY
Biessmann, H
机构
[1] NIEHS, Mol Genet Lab, Res Triangle Pk, NC 27709 USA
[2] Salk Inst Biol Studies, Mol Biol & Virol Lab, La Jolla, CA 92037 USA
[3] Univ Calif Irvine, Ctr Dev Biol, Irvine, CA 92697 USA
关键词
Drosophila; heterochromatin; silencing; TAS; telomere; transcription;
D O I
10.1023/A:1022925003172
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The terminal DNA arrays on chromosomes of Drosophila melanogaster are composed of two families of non-LTR retrotransposons, HeT-A and TART. Available evidence suggests that chromosome length in this species and its close relatives is maintained by targeted transposition of these elements, with attachment of the elements to the chromosome end by their 3' oligo(A) tails. However, the regulation of transposition of these elements and the control of telomere length are poorly understood. Here we present the hypothesis that the forces involved in telomere length regulation in Drosophila are the underlying forces that manifest themselves as telomeric position effect (TPE). Based on recent studies of TPE, which found that expression of a reporter gene is influenced by telomere structure in cis and trans, we propose that the subtelomeric satellite (TAS) in D. melanogaster plays an important role in controlling telomere elongation. Transcription of a HeT-A element is probably initiated at a promoter in the 3' UTR of an upstream element, and TAS may repress this transcriptional activity in cis and trans. A region of HeT-A not at the extreme 3' end of the element may act as a transcriptional enhancer that may be modulated by TAS.
引用
收藏
页码:319 / 325
页数:7
相关论文
共 31 条
[1]   The 3′ non-coding region of the Drosophila melanogaster HeT-A telomeric retrotransposon contains sequences with propensity to form G-quadruplex DNA [J].
Abad, JP ;
Villasante, A .
FEBS LETTERS, 1999, 453 (1-2) :59-62
[2]   THE GENOMIC ORGANIZATION OF HET-A RETROPOSONS IN DROSOPHILA-MELANOGASTER [J].
BIESSMANN, H ;
KASRAVI, B ;
JAKES, K ;
BUI, T ;
IKENAGA, K ;
MASON, JM .
CHROMOSOMA, 1993, 102 (05) :297-305
[3]   HET-A, A TRANSPOSABLE ELEMENT SPECIFICALLY INVOLVED IN HEALING BROKEN CHROMOSOME ENDS IN DROSOPHILA-MELANOGASTER [J].
BIESSMANN, H ;
VALGEIRSDOTTIR, K ;
LOFSKY, A ;
CHIN, C ;
GINTHER, B ;
LEVIS, RW ;
PARDUE, ML .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (09) :3910-3918
[4]   UbcD1, a Drosophila ubiquitin-conjugating enzyme required for proper telomere behavior [J].
Cenci, G ;
Rawson, RB ;
Belloni, G ;
Castrillon, DH ;
Tudor, M ;
Petrucci, R ;
Goldberg, LL ;
Wasserman, SA ;
Gatti, M .
GENES & DEVELOPMENT, 1997, 11 (07) :863-875
[5]  
Craven RJ, 1999, GENETICS, V152, P1531
[6]   Silencing at Drosophila telomeres:: nuclear organization and chromatin structure play critical roles [J].
Cryderman, DE ;
Morris, EJ ;
Biessmann, H ;
Elgin, SCR ;
Wallrath, LL .
EMBO JOURNAL, 1999, 18 (13) :3724-3735
[7]  
Danilevskaya ON, 1998, GENETICS, V148, P233
[8]   Promoting in tandem: The promoter for telomere transposon HeT-A and implications for the evolution of retroviral LTRs [J].
Danilevskaya, ON ;
Arkhipova, IR ;
Traverse, KL ;
Pardue, ML .
CELL, 1997, 88 (05) :647-655
[9]  
Danilevskaya ON, 1999, MOL CELL BIOL, V19, P873
[10]   EXPANSIONS OF TRANSGENE REPEATS CAUSE HETEROCHROMATIN FORMATION AND GENE SILENCING IN DROSOPHILA [J].
DORER, DR ;
HENIKOFF, S .
CELL, 1994, 77 (07) :993-1002