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来自菠菜叶绿体的含atpF II组内含子的基因在转基因衣藻叶绿体中未发生剪接。

The atpF group-II intron-containing gene from spinach chloroplasts is not spliced in transgenic Chlamydomonas chloroplasts.

作者信息

Deshpande N N, Hollingsworth M, Herrin D L

机构信息

Department of Botany, University of Texas at Austin 78713, USA.

出版信息

Curr Genet. 1995 Jul;28(2):122-7. doi: 10.1007/BF00315777.

Abstract

In order to determine whether the group-II trans-splicing machinery of the chloroplast of Chlamydomonas reinhardtii can splice a heterologous group-II cis intron, the atpF gene of spinach was transferred into the chloroplast genome of C. reinhardtii using the atpX expression vector. The atpF gene contains a group-II intron which, like other higher plant chloroplast introns, does not self-splice in vitro. The chimeric transgene was expressed at high levels, based on the accumulation of the precursor; however, spliced products could not be detected by Northern blotting, or by RT-PCR coupled with Southern-blot hybridization of the amplified products with an exon-junction probe. These results indicate that the spinach atpF intron is not spliced in transgenic C. reinhardtii chloroplasts. Thus, splicing of chloroplast introns mediated by cellular factors may be species-specific; alternately, the group-II splicing machinery of C. reinhardtii is specific for trans spliced introns.

摘要

为了确定莱茵衣藻叶绿体的II组反式剪接机制能否剪接异源II组顺式内含子,利用atpX表达载体将菠菜的atpF基因转入莱茵衣藻的叶绿体基因组中。atpF基因含有一个II组内含子,与其他高等植物叶绿体内含子一样,在体外不能自我剪接。基于前体的积累,嵌合转基因高水平表达;然而,通过Northern印迹法,或通过RT-PCR结合用外显子连接探针进行扩增产物的Southern印迹杂交,均未检测到剪接产物。这些结果表明,菠菜atpF内含子在转基因莱茵衣藻叶绿体中未发生剪接。因此,由细胞因子介导的叶绿体内含子剪接可能具有物种特异性;或者,莱茵衣藻的II组剪接机制对反式剪接内含子具有特异性。

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