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来自黑腹果蝇的功能性长散在核元件的种系表达:精细表征有助于对反式调节因子进行潜在研究。

Germ-line expression of a functional LINE from Drosophila melanogaster: fine characterization allows for potential investigations of trans-regulators.

作者信息

Tatout C, Docquier M, Lachaume P, Mesure M, Lécher P, Pinon H

机构信息

Laboratoire de Génétique, Université Blaise Pascal, Aubière, France.

出版信息

Int J Dev Biol. 1994 Mar;38(1):27-33.

PMID:8074994
Abstract

The I factor (IF) is a functional non-viral retrotransposon, or LINE, from Drosophila melanogaster. It is mobilized in the germ-line of dysgenic SF females during I-R hybrid dysgenesis. In previous papers (Lachaume et al., Development 115: 729-735, 1992; Lachaume and Pinon, Mol. Gen. Gen. 240: 277-285, 1993) we used a transgenic fusion between the 5' part of the IF and the lacZ gene to characterize IF expression and its regulation. This I-lacZ transgenic fusion expresses beta-galactosidase activity during oogenesis. We established a Drosophila line bearing four transgenic insertions (the 4I-lacZ line) and got new insights about IF expression: (1) I-lacZ expression is proportional to the copy number of transgenes present in the genome, (2) the expression occurs just before or when meiosis begins, (3) this expression seems to be subjected to a variegation effect within the germ-line cells, (4) the transgenic activity is mainly directed toward the decondensed chromatin of nurse cells. The close relationship between I factor expression and oogenesis led us to investigate the role played by genes expressed during oogenesis on I factor expression. We present recent data indicating that mutants which interfere with oogenesis can also affect I factor expression. From this data we propose an original screen using the 41-lacZline to detect identified mutations which also affect I factor expression.

摘要

I因子(IF)是一种来自黑腹果蝇的功能性非病毒逆转座子,即长散在核元件(LINE)。在I-R杂种不育过程中,它在不育的SF雌性生殖系中被激活。在之前的论文中(Lachaume等人,《发育》115: 729 - 735,1992;Lachaume和Pinon,《分子遗传学与基因组学》240: 277 - 285,1993),我们利用IF 5'部分与lacZ基因之间的转基因融合来表征IF的表达及其调控。这种I-lacZ转基因融合在卵子发生过程中表达β-半乳糖苷酶活性。我们建立了一个带有四个转基因插入片段的果蝇品系(4I-lacZ品系),并对IF的表达有了新的认识:(1)I-lacZ的表达与基因组中存在的转基因拷贝数成正比,(2)表达发生在减数分裂开始之前或开始时,(3)这种表达似乎在生殖系细胞中受到斑驳效应的影响,(4)转基因活性主要针对滋养细胞的解聚染色质。I因子表达与卵子发生之间的密切关系促使我们研究卵子发生过程中表达的基因对I因子表达所起的作用。我们展示了最近的数据,表明干扰卵子发生的突变体也会影响I因子的表达。基于这些数据,我们提出了一种利用4I-lacZ品系进行的原始筛选方法,以检测也会影响I因子表达的已鉴定突变。

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