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Ds1转座元件在突变等位基因Adh1-Fm335中充当内含子,并从信使RNA中剪接出来。

The Ds1 transposable element acts as an intron in the mutant allele Adh1-Fm335 and is spliced from the message.

作者信息

Dennis E S, Sachs M M, Gerlach W L, Beach L, Peacock W J

机构信息

CSIRO, Division of Plant Industry, Canberra ACT, Australia.

出版信息

Nucleic Acids Res. 1988 May 11;16(9):3815-28. doi: 10.1093/nar/16.9.3815.

Abstract

The Ds-induced maize Adh1 allele Adh1-Fm335 retains its anaerobic regulation and normal transcription start site despite the presence of the 405 bp Ds element in the 5' untranslated leader region of the gene. The steady state level of Adh1-specific transcript is reduced to about 1% that of the progenitor or revertant alleles. Run-on transcription studies show that the reduced level of Adh1 specific mRNA is not attributable to a decreased transcription rate. S1 mapping indicates that the Ds element is spliced from the Adh1-Fm335 transcript using a donor site 14 bp into the Ds element and an acceptor site at the 3' junction of the Ds element with the flanking genome DNA.

摘要

尽管在基因的5'非翻译前导区存在405 bp的Ds元件,但Ds诱导的玉米Adh1等位基因Adh1-Fm335仍保留其厌氧调节和正常转录起始位点。Adh1特异性转录本的稳态水平降至祖代或回复等位基因的约1%。核连缀转录研究表明,Adh1特异性mRNA水平的降低并非归因于转录速率的下降。S1图谱分析表明,Ds元件是从Adh1-Fm335转录本中剪接出来的,使用的供体位点位于Ds元件内14 bp处,受体位点位于Ds元件与侧翼基因组DNA的3'连接处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f3b2/336558/e5e58e2585ce/nar00152-0223-a.jpg

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