Staub J M, Maliga P
Waksman Institute, Rutgers, State University of New Jersey, Piscataway 08855-0759.
Plant J. 1994 Oct;6(4):547-53. doi: 10.1046/j.1365-313x.1994.6040547.x.
The plastid psbA gene encodes the 32 kDa D1 polypeptide of photosystem II. It has previously been shown that the initiation of psbA mRNA translation in tobacco is regulated by sequences outside of the coding region. To identify the cis-acting regulatory sequences involved in the translational control, a series of chimeric uidA genes, encoding the beta-glucuronidase (GUS) reporter enzyme, were introduced into the plastid genome. GUS accumulation in response to the light (135- to 200-fold), and the arrest of uidA mRNA translation in light-grown seedlings following transfer for 2 h to the dark, was observed only if the transgenes contained the psbA 5'-untranslated leader region (UTR). Changes in GUS accumulation were accompanied by little or no changes in the uidA mRNA levels. The data indicate that the initiation of D1 translation in tobacco plastids is controlled via the psbA 5'-UTR.
质体psbA基因编码光系统II的32 kDa D1多肽。先前已表明,烟草中psbA mRNA翻译的起始受编码区以外的序列调控。为了鉴定参与翻译控制的顺式作用调控序列,将一系列编码β-葡萄糖醛酸酶(GUS)报告酶的嵌合uidA基因导入质体基因组。仅当转基因包含psbA 5'-非翻译前导区(UTR)时,才观察到GUS响应光照而积累(135至200倍),以及在光照下生长的幼苗转移到黑暗中2小时后uidA mRNA翻译的停滞。GUS积累的变化伴随着uidA mRNA水平很少或没有变化。数据表明,烟草质体中D1翻译的起始是通过psbA 5'-UTR控制的。