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果蝇两个热休克基因座的转录

Transcription at two heat shock loci in Drosophila.

作者信息

Henikoff S, Meselson M

出版信息

Cell. 1977 Oct;12(2):441-51. doi: 10.1016/0092-8674(77)90120-9.

DOI:10.1016/0092-8674(77)90120-9
PMID:410501
Abstract

Transcription at two heat shock loci in Drosophila melanogaster, in subdivisions 87A and 57C, was investigated by hybridization in situ with 3H-labeled messenger, nuclear RNA and whole cell RNA from cells cultured at elevated temperature. What appears to be the same 9 x 10(5) dalton heat shock message hybridizes at both sites. At 87a, little additional hybridization is obtained with nuclear or whole cell RNA. In contrast, at 87C the saturation level of hybridization by nuclear and whole cell RNA is much higher than that obtained with the message alone. This evidence for extensive hybridization at 87C but not at 87A by RNA distinct from the message is confirmed by the finding that excess nonradioactive message competes away most of the hybridization by 3H-labeled nuclear and whole cell RNA at the latter locus but not at the former. The noncompetable RNA migrates on an electrophoretic gel as a heterogeneous population of molecules, extending to sizes both larger and smaller than the message. These and other observations lead to the conclusion that a 87A transcription includes little more than sequences complementary to the 9 x 10(5) dalton message, while at 87C, there are sequences complementary to the same message and extensive additional sequences complementary to other species of RNA.

摘要

利用来自高温培养细胞的3H标记信使RNA、核RNA和全细胞RNA进行原位杂交,研究了黑腹果蝇87A和57C区域中两个热休克基因座的转录情况。在这两个位点杂交的似乎是相同的9×10⁵道尔顿热休克信使RNA。在87A位点,用核RNA或全细胞RNA进行杂交时几乎没有额外的杂交信号。相反,在87C位点,核RNA和全细胞RNA的杂交饱和水平比单独用信使RNA杂交时高得多。过量的非放射性信使RNA能竞争掉3H标记的核RNA和全细胞RNA在87C位点的大部分杂交信号,但在87A位点则不能,这一发现证实了在87C位点存在大量与信使RNA不同的RNA杂交,而在87A位点则没有。不可竞争的RNA在电泳凝胶上迁移时呈现出分子大小不均一的群体,其大小既有比信使RNA大的,也有比信使RNA小的。这些观察结果以及其他一些观察结果得出这样的结论:87A位点的转录产物中几乎只有与9×10⁵道尔顿信使RNA互补的序列,而在87C位点,既有与相同信使RNA互补的序列,也有与其他种类RNA互补的大量额外序列。

相似文献

1
Transcription at two heat shock loci in Drosophila.果蝇两个热休克基因座的转录
Cell. 1977 Oct;12(2):441-51. doi: 10.1016/0092-8674(77)90120-9.
2
Sequence organization and transcription at two heat shock loci in Drosophila.果蝇两个热休克基因座的序列组织与转录
Proc Natl Acad Sci U S A. 1978 Nov;75(11):5613-7. doi: 10.1073/pnas.75.11.5613.
3
In situ quantification of hsp70 and alpha-beta transcripts at 87A and 87C loci in relation to hsr-omega gene activity in polytene cells of Drosophila melanogaster.在黑腹果蝇多线细胞中,与热休克RNA-ω(hsr-omega)基因活性相关的87A和87C位点处hsp70和α-β转录本的原位定量分析。
Chromosome Res. 1995 Sep;3(6):386-93. doi: 10.1007/BF00710021.
4
Studies of cloned sequences from four Drosophila heat shock loci.来自四个果蝇热休克基因座的克隆序列研究。
Cell. 1979 Dec;18(4):1359-70. doi: 10.1016/0092-8674(79)90246-0.
5
Two hybrid plasmids with D. melanogaster DNA sequences complementary to mRNA coding for the major heat shock protein.两个杂交质粒,其具有与编码主要热休克蛋白的mRNA互补的黑腹果蝇DNA序列。
Cell. 1978 Aug;14(4):921-9. doi: 10.1016/0092-8674(78)90346-x.
6
Transcription and metabolism of RNA from the Drosophila melanogaster heat shock puff site 93D.果蝇热休克疏松位点93D的RNA转录与代谢
Chromosoma. 1980;80(3):237-52. doi: 10.1007/BF00292683.
7
Dosage compensation of X-linked heat-shock puffs in Drosophila pseudoobscura.果蝇拟暗果蝇中X连锁热休克疏松区的剂量补偿
Chromosoma. 1980;76(3):245-54. doi: 10.1007/BF00327265.
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Expression of 87A, 87C and 93D heat shock puffs in trisomic (2L and 3L) strains of Drosophila melanogaster: evidence for a functional relation between 93D and 87C.87A、87C和93D热休克胀泡在黑腹果蝇三体(2L和3L)品系中的表达:93D与87C之间功能关系的证据
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Localization and expression of transformed DNA sequences within heat shock puffs of Drosophila melanogaster.黑腹果蝇热休克胀泡内转化DNA序列的定位与表达
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Deletion mapping of two D. melanogaster loci that code for the 70,000 dalton heat-induced protein.对两个编码70,000道尔顿热诱导蛋白的黑腹果蝇基因座进行缺失定位。
Cell. 1979 Jul;17(3):565-71. doi: 10.1016/0092-8674(79)90264-2.

引用本文的文献

1
Quantitative analysis of the heat shock response of Saccharomyces cerevisiae.酿酒酵母热休克反应的定量分析。
J Bacteriol. 1982 Jul;151(1):311-27. doi: 10.1128/jb.151.1.311-327.1982.
2
Localization of a unique gene by direct hybridization in situ.通过直接原位杂交对一个独特基因进行定位。
Proc Natl Acad Sci U S A. 1981 Jun;78(6):3755-9. doi: 10.1073/pnas.78.6.3755.
3
Heat shock alters nuclear ribonucleoprotein assembly in Drosophila cells.热休克改变果蝇细胞中的核糖核蛋白组装。
Mol Cell Biol. 1983 Feb;3(2):161-71. doi: 10.1128/mcb.3.2.161-171.1983.
4
Drosophila gene related to the major heat shock-induced gene is transcribed at normal temperatures and not induced by heat shock.与主要热休克诱导基因相关的果蝇基因在正常温度下转录,且不受热休克诱导。
Proc Natl Acad Sci U S A. 1982 Jan;79(2):525-9. doi: 10.1073/pnas.79.2.525.
5
Quantitative in situ hybridization reveals extent of sequence homology between related DNA sequences in Drosophila melanogaster.定量原位杂交揭示了黑腹果蝇中相关DNA序列之间的序列同源程度。
Chromosoma. 1981;83(2):159-68. doi: 10.1007/BF00286786.
6
Sequence homologies in the 5' regions of four Drosophila heat-shock genes.四种果蝇热休克基因5'区域的序列同源性。
Proc Natl Acad Sci U S A. 1981 Jun;78(6):3775-8. doi: 10.1073/pnas.78.6.3775.
7
Isolation and characterization of nuclear ribonucleoprotein complexes from Drosophila melanogaster.黑腹果蝇核糖核蛋白复合体的分离与鉴定
Mol Biol Rep. 1981 May 22;7(1-3):5-13. doi: 10.1007/BF00778727.
8
Monoclonal antibody directed against RNA polymerase II of Drosophila melanogaster.针对黑腹果蝇RNA聚合酶II的单克隆抗体。
Mol Gen Genet. 1980;180(1):193-9. doi: 10.1007/BF00267369.
9
Acetylation and methylation patterns of core histones are modified after heat or arsenite treatment of Drosophila tissue culture cells.果蝇组织培养细胞经热或亚砷酸盐处理后,核心组蛋白的乙酰化和甲基化模式会发生改变。
Nucleic Acids Res. 1983 Mar 11;11(5):1389-404. doi: 10.1093/nar/11.5.1389.
10
Localization of the ribosomal genes in Caenorhabditis elegans chromosomes by in situ hybridization using biotin-labeled probes.使用生物素标记的探针通过原位杂交将核糖体基因定位到秀丽隐杆线虫染色体上。
EMBO J. 1984 Jun;3(6):1227-34. doi: 10.1002/j.1460-2075.1984.tb01957.x.