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温度冲击对美洲大蚊(双翅目:大蚊科)转录和复制的影响

The effects of temperature shock on transcription and replication in Rhynchosciara americana (Diptera: Sciaridae).

作者信息

Stocker Ann Jacob, Madalena Christiane R G, Gorab Eduardo

机构信息

Departmento de Biologia, Instituto de Biociências, Universidade de São Paulo, Rua do Matão, 277, Cidade Universitária, CEP 05508-090, São Paulo, Brazil.

出版信息

Genetica. 2006 Mar;126(3):277-90. doi: 10.1007/s10709-005-7407-8.

DOI:10.1007/s10709-005-7407-8
PMID:16636922
Abstract

The chromosomal response to temperature shock in Rhynchosciara americana is similar to that observed in other Diptera. After a 33 degrees C/90 min or a 36 degrees C/30 min shock the reaction for RNA polymerase II (RpII) is enhanced at five loci. The most prominent of these was identified by in situ hybridization as the site of the hsp70 gene. At 33 degrees C, an accumulation of heat shock factor (HSF) and an increase in the level of RpII was observed at some heat shock loci after 5 min and reached a maximum after 15 min at most loci. The pattern of accumulation of HSF and RpII at individual heat shock loci was similar and their increases were generally coordinated among the loci. RpII gradually decreased at sites active prior to shock, the rate of decrease varying with the site. The B2 DNA puff retained RpII for a significant length of time while the histone locus still contained RpII after a shock of 90 min. With a 36 degrees C/30 min shock, the size of the heat shock puffs and the intensities of HSF and RpII peaked at 1-4 h post stress. The level of HSF declined rapidly after 1 h while the level of RpII remained high for an additional 4 h. The reaction of the DNA puffs to heat shock varied. Usually they did not regress completely and retained traces of RpII. BrdU incorporation continued at both amplifying and non-amplifying bands after shock but on average it appeared depressed for about 24 h post stress.

摘要

美洲大蠊染色体对温度休克的反应与其他双翅目昆虫中观察到的相似。在33℃/90分钟或36℃/30分钟的休克处理后,RNA聚合酶II(RpII)在五个位点的反应增强。其中最显著的位点通过原位杂交被鉴定为hsp70基因的位点。在33℃时,5分钟后在一些热休克位点观察到热休克因子(HSF)的积累和RpII水平的增加,大多数位点在15分钟后达到最大值。单个热休克位点上HSF和RpII的积累模式相似,并且它们的增加在各个位点之间通常是协同的。休克前活跃的位点上RpII逐渐减少,减少速率因位点而异。B2 DNA胀泡在相当长的时间内保留RpII,而组蛋白位点在90分钟的休克处理后仍含有RpII。在36℃/30分钟的休克处理后,热休克胀泡的大小以及HSF和RpII的强度在应激后1 - 4小时达到峰值。1小时后HSF水平迅速下降,而RpII水平在另外4小时内仍保持较高。DNA胀泡对热休克的反应各不相同。通常它们不会完全消退,并保留RpII的痕迹。休克后,在扩增带和非扩增带处BrdU掺入均持续,但平均而言,应激后约24小时掺入似乎受到抑制。

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