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黑曲霉葡糖淀粉酶基因中的两种不同类型的间隔序列。

Two different types of intervening sequences in the glucoamylase gene from Aspergillus niger.

作者信息

Boel E, Hansen M T, Hjort I, Høegh I, Fiil N P

出版信息

EMBO J. 1984 Jul;3(7):1581-5. doi: 10.1002/j.1460-2075.1984.tb02014.x.

Abstract

One single glucoamylase gene could be identified in the chromosomal DNA of Aspergillus niger by Southern blot analysis. This glucoamylase gene was isolated from a genomic library of A. niger DNA. The glucoamylase gene is situated on a 2.5-kb EcoRI-EcoRV fragment and contains five intervening sequences in the coding region. One 169-bp intron is involved in differential mRNA processing leading to the two different glucoamylase enzymes G1 and G2; the other four introns are all very small ranging from 55 to 75 bp in length. One intron has a significant homology to the coding region which immediately follows, and it contains the internal conserved sequence TACTAAC, which is also found in yeast chromosomal gene introns, and is thought to participate in mRNA splicing. Two transcription initiation sites and a typical eukaryotic promoter region with TATAAT and CAAT boxes are located upstream from the gene.

摘要

通过Southern印迹分析可在黑曲霉的染色体DNA中鉴定出一个单一的葡糖淀粉酶基因。该葡糖淀粉酶基因是从黑曲霉DNA的基因组文库中分离出来的。葡糖淀粉酶基因位于一个2.5kb的EcoRI - EcoRV片段上,在编码区含有五个间隔序列。一个169bp的内含子参与导致两种不同葡糖淀粉酶G1和G2的差异mRNA加工;其他四个内含子都非常小,长度在55至75bp之间。一个内含子与紧随其后的编码区具有显著的同源性,并且它包含内部保守序列TACTAAC,该序列也存在于酵母染色体基因内含子中,并且被认为参与mRNA剪接。两个转录起始位点以及一个带有TATAAT和CAAT框的典型真核启动子区域位于该基因的上游。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d651/557562/371af9c20b36/emboj00311-0135-a.jpg

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