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通过v-myc探针检测到的发育调控的、母体表达的果蝇RNA种类家族。

Family of developmentally regulated, maternally expressed Drosophila RNA species detected by a v-myc probe.

作者信息

Madhavan K, Bilodeau-Wentworth D, Wadsworth S C

出版信息

Mol Cell Biol. 1985 Jan;5(1):7-16. doi: 10.1128/mcb.5.1.7-16.1985.

Abstract

Drosophila melanogaster genomic sequences that hybridize with v-myc have been reported (B.-Z. Shilo and R. A. Weinberg, Proc. Natl. Acad. Sci. U.S.A. 78:6789-6792, 1981). We have detected Drosophila RNA sequences that also hybridize with v-myc. In an attempt to characterize these RNA sequences, we used v-myc hybridization probes to isolate Drosophila genomic segments. None of the Drosophila genomic or cDNA clones that we have isolated hybridize with the 3' exon of v-myc. Preliminary nucleotide sequence analyses have revealed sufficient homology to account for the observed hybridization between v-myc and the Drosophila clones but have failed to detect significant amino acid sequence homology. Thus is seems unlikely that the mRNA sequences or the genomic sequences that we have isolated by hybridization with v-myc represent homologs of the vertebrate myc gene. Despite the lack of structural homology between the cloned Drosophila sequences and v-myc, we have investigated the pattern of expression of those RNA species that hybridize with v-myc. Polyadenylic acid-containing transcripts of 2.7, 2.2, and 1.7 kilobases (kb) in embryos, pupae, adults, and Kc cells and an additional 1.4-kb transcript in adults were complementary to the Drosophila genomic clones and to v-myc. The 1.7- and 2.2-kb transcripts were localized on polyribosomes in Kc cells. The 1.7- and 2.2-kb transcripts were present after 45 min, 2 h, and 4 h of embryonic development, but by 16 h of development their levels had decreased by more than sixfold. During metamorphosis, two peaks of expression of the 1.7- and 2.2-kb transcripts were observed, at 6 and 72 h postpupariation. The 1.4-kb RNA species was first detected at 72 h postpupariation. In adults, the 1.7- and 2.2-kb transcripts were detected only in ovaries in females, whereas the 1.4-kb transcript was present in female nonovarian RNA and in males. These results suggest that the transcripts in early embryos are of maternal origin.

摘要

已有报道称黑腹果蝇基因组序列能与v-myc杂交(B.-Z. 希洛和R. A. 温伯格,《美国国家科学院院刊》78:6789 - 6792, 1981)。我们检测到果蝇RNA序列也能与v-myc杂交。为了对这些RNA序列进行表征,我们使用v-myc杂交探针分离果蝇基因组片段。我们分离得到的果蝇基因组或cDNA克隆均未与v-myc的3'外显子杂交。初步的核苷酸序列分析显示出足够的同源性,能够解释v-myc与果蝇克隆之间观察到的杂交现象,但未能检测到显著的氨基酸序列同源性。因此,通过与v-myc杂交分离得到的mRNA序列或基因组序列似乎不太可能代表脊椎动物myc基因的同源物。尽管克隆的果蝇序列与v-myc之间缺乏结构同源性,但我们研究了那些与v-myc杂交的RNA种类的表达模式。胚胎、蛹、成虫和Kc细胞中2.7、2.2和1.7千碱基(kb)含聚腺苷酸的转录本,以及成虫中另外一种1.4-kb转录本与果蝇基因组克隆和v-myc互补。1.7-kb和2.2-kb转录本定位于Kc细胞的多核糖体上。1.7-kb和2.2-kb转录本在胚胎发育45分钟、2小时和4小时后出现,但到发育16小时时其水平下降了超过六倍。在变态过程中,观察到1.7-kb和2.2-kb转录本在化蛹后6小时和72小时出现两个表达高峰。1.4-kb RNA种类在化蛹后72小时首次被检测到。在成虫中,1.7-kb和2.2-kb转录本仅在雌性卵巢中检测到,而1.4-kb转录本存在于雌性非卵巢RNA和雄性中。这些结果表明早期胚胎中的转录本来源于母体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acf3/366671/771155da36a0/molcellb00097-0027-a.jpg

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