Nucleotide sequences of two soybean U1 snRNA genes.
نویسندگان
چکیده
Southern blot analyses show that the soybean genome contains many U1 snRNA genes, both in tandem arrays and as isolated genes. We have cloned and sequenced two soybean U1 snRNA genes, U1a and U1b, which represent distinct multicopy tandem repeat elements. Sequence analysis of the first 46 nt of soybean embryo protoplast U1 snRNA by primer extension shows that sequences corresponding to U1a and U1b are present in approximately equal proportions. Soybean U1a and U1b snRNA sequences, shown aligned to maximize homolgy, are both very similar to common bean U1 snRNA (1). Plus signs indicate sequences common to all three genes; dots indicate bases identical between the two soybean genes. The predicted secondary structure and sequences of the single-stranded 5 end, loops (indicated by Roman numerals in brackets), and Sm binding site are virtually identical to those of other U1 snRNAs (1). The 5' flanking regions of the two soybean U1 snRNA genes exhibit 7 1 % homology, mostly concentrated in blocks of identity. A "TATAAA" sequence occurs 3126 bases 5' to both genes. Blocks of sequences shared by common bean U1 and soybean U1 a and U1 b snRNA genes (indicated by + in the figure) occur as far as 228 bases 5' to the U1 snRNA gene. One shared sequence (TCCCACATCG, underlined in figure) also occurs 5 to several Arabidopsis thaliana U2 snRNA genes and is required for their expression (2). However, we have been unable to detect transcription of the cloned soybean U1a and U1b genes when introduced into soybean embryo or tobacco leaf protoplasts.
منابع مشابه
The Myb domain of the largest subunit of SNAPc adopts different architectural configurations on U1 and U6 snRNA gene promoter sequences
The small nuclear RNA (snRNA) activating protein complex (SNAPc) is essential for transcription of genes that encode the snRNAs. Drosophila melanogaster SNAPc (DmSNAPc) consists of three subunits (DmSNAP190, DmSNAP50 and DmSNAP43) that form a stable complex that recognizes an snRNA gene promoter element called the PSEA. Although all three subunits are required for sequence-specific DNA binding ...
متن کاملU1 small nuclear ribonucleoprotein particle-protein interactions are revealed in Saccharomyces cerevisiae by in vivo competition assays.
Two highly conserved regions of the 586-nucleotide yeast (Saccharomyces cerevisiae) U1 small nuclear RNA (snRNA) can be mutated or deleted with little or no effect on growth rate: the universally conserved loop II (corresponding to the metazoan A loop) and the yeast core region (X. Liao, L. Kretzner, B. Séraphin, and M. Rosbash, Genes Dev. 4:1766-1774, 1990). To examine the contribution of thes...
متن کاملA conserved intronic U1 snRNP-binding sequence promotes trans-splicing in Drosophila.
Unlike typical cis-splicing, trans-splicing joins exons from two separate transcripts to produce chimeric mRNA and has been detected in most eukaryotes. Trans-splicing in trypanosomes and nematodes has been characterized as a spliced leader RNA-facilitated reaction; in contrast, its mechanism in higher eukaryotes remains unclear. Here we investigate mod(mdg4), a classic trans-spliced gene in Dr...
متن کاملGene expression profiling reveals U1 snRNA regulates cancer gene expression
U1 small nuclear RNA (U1 snRNA), as one of the most abundant ncRNAs in human cells, plays an important role in splicing of pre-mRNAs. Compared to previous studies which have focused on the primary function of U1 snRNA and the neurodegenerative diseases caused by abnormalities of U1 snRNA, this study is to investigate how U1 snRNA over-expression affects the expression of mammal genes on a genom...
متن کاملDetection of genetic polymorphism among and within Echinococcus granulosus strains by heteroduplex analysis of a microsatellite from the U1 snRNA genes.
Polymerase chain reaction of a pentanucleotide microsatellite in the U1 snRNA gene complex generated a multiple band pattern due to the priming of paralogous sequences. Denaturation and slow renaturation of polymerase chain reaction products allow the formation of heteroduplex DNA that can be detected by its differential mobility in polyacrylamide gel electrophoresis. Heteroduplex analysis was ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Nucleic acids research
دوره 16 9 شماره
صفحات -
تاریخ انتشار 1988