Carter C E, Szmidt-Jaworska A, Hughes M, Thomas B, Jackson S
Plant Genetics and Biotechnology Department, Horticulture Research International, Wellesbourne, Warwick, UK.
J Exp Bot. 2000 Apr;51(345):703-11.
The exposure of dark-grown Pharbitis nil seedlings to continuous R induces a rapid decrease in PHYA mRNA abundance with a half-life of about 2 h. A 5 min R pulse also induces this decline, and the effect is partially reversible by subsequent FR irradiation, confirming that the regulation of expression is mediated via the Pfr form of a phytochrome. When de-etiolated seedlings are returned to darkness after a W photoperiod, PHYA mRNA slowly reaccumulates from 20% to 50% of the dark level within 24 h. The rate of reaccumulation is greatly accelerated by the removal of Pfr with a FR pulse, resulting in reaccumulation to 100% within approximately 11 h. Without FR irradiation PHYA mRNA expression remains fully repressed for at least 11 h after the end of the photoperiod, suggesting that the controlling Pfr is highly stable.
将黑暗中生长的牵牛花幼苗置于持续的红光下,会导致PHYA mRNA丰度迅速下降,半衰期约为2小时。5分钟的红光脉冲也会诱导这种下降,并且随后的远红光照射可部分逆转这种效应,这证实了表达调控是通过光敏色素的Pfr形式介导的。当脱黄化幼苗在白光光周期后返回黑暗中时,PHYA mRNA在24小时内从黑暗水平的20%缓慢重新积累到50%。用远红光脉冲去除Pfr可大大加速重新积累的速率,从而在约11小时内重新积累到100%。在没有远红光照射的情况下,光周期结束后PHYA mRNA表达至少11小时仍完全受到抑制,这表明起控制作用的Pfr非常稳定。