THE DROSOPHILA-MICROPIA RETROTRANSPOSON ENCODES A TESTIS-SPECIFIC ANTISENSE RNA COMPLEMENTARY TO REVERSE-TRANSCRIPTASE

被引:70
作者
LANKENAU, S [1 ]
CORCES, VG [1 ]
LANKENAU, DH [1 ]
机构
[1] JOHNS HOPKINS UNIV, DEPT BIOL, BALTIMORE, MD 21218 USA
关键词
D O I
10.1128/MCB.14.3.1764
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
The micropia transposable element of Drosaphila hydei is a long terminal repeat-containing retrotransposon present in both the autosomes and the Y chromosome. micropia expression gives rise to a complex set of sense and antisense RNAs transcribed primarily during spermatogenesis. The most abundant sense RNAs constitute an assortment of heterogeneous high-molecular-weight transcripts expressed as constituents of the Y-chromosomal lampbrush loops of primary spermatocytes. In addition, micropia encodes a full-length RNA that extends between the two long terminal repeats of the element. The major l.O-kb antisense RNA characterized is complementary to the reverse transcriptase and RNase H coding regions of micropia, It is expressed from a testis-specific promoter during the primary spermatocyte stages and is detectable until spermatid elongation stages. Sequence comparison of this promoter with the 5' region of other testis-specific genes allows the conception of a conserved sequence that is responsible for this pattern of expression. A 284-bp fragment containing this sequence is able to drive testis-specific expression of the Escherichia coli lacZ gene in Drosophila melanogaster. This sequence is conserved in the micropia elements present in other Drosophila species that also encode an antisense RNA. The evolutionary conservation of micropia antisense RNA expression and the sequences responsible for its testis-specific transcription suggests a role for this antisense RNA in the control of germ line expression of the full-length transcript or transposon-encoded proteins.
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页码:1764 / 1775
页数:12
相关论文
共 51 条
[2]   NEW COMPOUND (1) CHROMOSOMES AND PRODUCTION OF LARGE QUANTITIES OF X-O MALES IN DROSOPHILA-HYDEI [J].
BECK, H .
GENETICS RESEARCH, 1975, 26 (03) :313-317
[3]  
BOEKE JD, 1989, ANNU REV MICROBIOL, V43, P403, DOI 10.1146/annurev.micro.43.1.403
[4]  
BOORSTEIN WR, 1989, METHOD ENZYMOL, V180, P347
[5]   LAMPBRUSH CHROMOSOME LOOP-SPECIFICITY OF TRANSCRIPT MORPHOLOGY IN SPERMATOCYTE NUCLEI OF DROSOPHILA-HYDEI [J].
DELOOS, F ;
DIJKHOF, R ;
GROND, CJ ;
HENNIG, W .
EMBO JOURNAL, 1984, 3 (12) :2845-2849
[6]  
DORIG R, 1991, THESIS U ZURICH ZURI
[7]  
Engels WR, 1989, MOBILE DNA, P437
[8]  
FINNEGAN DJ, 1989, MOBILE DNA, P503
[9]  
FINNEGAN DJ, 1986, OXFORD SURVEYS EUKAR, P1
[10]  
FULLER M, 1993, DEV DROSOPHILA MELAN, P1