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大豆核酮糖-1,5-二磷酸羧化酶小亚基基因家族两个高度同源成员的表达比较

Comparison of the expression of two highly homologous members of the soybean ribulose-1,5-bisphosphate carboxylase small subunit gene family.

作者信息

Shirley B W, Ham D P, Senecoff J F, Berry-Lowe S L, Zurfluh L L, Shah D M, Meagher R B

机构信息

Department of Genetics, University of Georgia, Athens 30602.

出版信息

Plant Mol Biol. 1990 Jun;14(6):909-25. doi: 10.1007/BF00019389.

Abstract

Two soybean ribulose-1,5-bisphosphate carboxylase small subunit (SSU) genes, SRS1 and SRS4, are highly homologous over a region that includes 4 kb of 5' and 1 kb of 3' flanking sequences. The expression of these genes was compared using synthetic oligonucleotide probes. Analysis of a soybean leaf cDNA library indicates that SRS1 and SRS4 are the most highly expressed members of the soybean SSU gene family. Similar changes were observed in the RNA levels for these genes in response to white light, far-red light and darkness, although SRS1 was expressed at a four-fold higher level in total RNA than SRS4 under all conditions. However, nuclear run-on assays indicate that SRS1 is transcribed at a lower rate than SRS4, which suggests that SRS1 RNA is more stable. S1 nuclease analysis and oligonucleotide directed RNase H cleavage indicate that transcripts from both genes are polyadenylated within two principle regions separated by 35 nt. Sequence analysis of 16 independent cDNA clones identified seven different polyadenylation sites, and six of these sites lie within these two regions. Although SRS1 RNA was poorly recovered during poly(A)+ fractionation, RNase H cleavage experiments showed that transcripts from SRS1 and SRS4 had similar poly (A) tail lengths ranging from 0 to 220 nt. In addition, and despite differences in the untranslated leader sequences, SRS1 and SRS4 RNAs are assembled into polysomes with equal efficiencies. The overall similarity in expression patterns for these two genes further illustrates the coordinate evolution of individual members of a SSU gene family and is consistent with the proposal that gene conversion homogenizes both the coding and regulatory regions of these genes.

摘要

两个大豆核酮糖-1,5-二磷酸羧化酶小亚基(SSU)基因,SRS1和SRS4,在一个包括4 kb的5'侧翼序列和1 kb的3'侧翼序列的区域内高度同源。使用合成寡核苷酸探针比较了这些基因的表达。对大豆叶片cDNA文库的分析表明,SRS1和SRS4是大豆SSU基因家族中表达水平最高的成员。尽管在所有条件下SRS1在总RNA中的表达水平比SRS4高四倍,但在白光、远红光和黑暗条件下,这些基因的RNA水平观察到类似的变化。然而,细胞核连续转录分析表明,SRS1的转录速率低于SRS4,这表明SRS1 RNA更稳定。S1核酸酶分析和寡核苷酸定向RNase H切割表明,两个基因的转录本在由35 nt隔开的两个主要区域内进行多聚腺苷酸化。对16个独立cDNA克隆的序列分析确定了7个不同的多聚腺苷酸化位点,其中6个位点位于这两个区域内。尽管在poly(A)+分级分离过程中SRS1 RNA的回收率很低,但RNase H切割实验表明,SRS1和SRS4的转录本具有相似的多聚(A)尾长度,范围从0到220 nt。此外,尽管非翻译前导序列存在差异,但SRS1和SRS4 RNA以相同的效率组装到多核糖体中。这两个基因表达模式的总体相似性进一步说明了SSU基因家族单个成员的协同进化,并且与基因转换使这些基因的编码区和调控区同质化的提议一致。

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