PubMed Health⌕ Search

Biomedical subjects

Si Shi Shen

Publications and source records attributed to Si Shi Shen.

2 recordsLinked to original sources

[Isolation and expression pattern analysis of rice auxin-induced eIF3a coding gene].

Eukaryotic initiation factors (eIFs) are key elements in protein synthesis. Among identified 13 initiation factors, eIF3, composed of 8 or more subunits, is the largest one and plays a central role in the initiation of translation. As the largest subunit, eIF3a mediates most functions of eIF3. Based on the experiments that rice eIF3a gene could be induced by auxin (through fluorescent differential display PCR), a cDNA coding for rice eIF3a, named OseIF3a1, was isolated. OseIF3a1 cDNA, with a length of 3459 bp (including 5' and 3'-UTR) and encoding a 986-aa polypeptide, shared sequence identity of 82.4% and 70.1% with that in maize and tobacco. Comparison of cDNA and genomic sequence revealed the presence of 13 exons and 12 introns in OseIF3a1 gene. Reverse transcript PCR (RT-PCR) analysis indicated the expression of OseIF3a1 in root, shoots, young spike, stem and leaf tissues, promoter-GUS fusion studies further confirmed its expression in root tip, leaf, glume and stigma. The induction of OseIF3a1 by auxin suggested that function of auxin on growth may involve the regulation on translation level.

Amino Acid Sequence↗

[Isolation of ABA-regulated genes in Oryza sativa through fluorescent differential display PCR (FDD-PCR)].

Abscisic acid (ABA) was critical in plant seed development and response to environmental factors such as stress situations. To study the possible ABA related signaling transduction pathways, we tried to isolate the ABA-regulated genes through fluorescent differential display PCR (FDD-PCR) technology using rice seedling as materials (treated with ABA for 2, 4, 8 and 12h). In the 17 fragments isolated, 14 and 3 clones were up-and down-regulated respectively. Sequence analyses revealed that the encoded proteins were involved in photosynthesis (7 fragments), signal transduction (1 fragments), transcription (2 fragments), metabolism and resistance (6 fragments), and unknown protein (1 fragments). 3 clones, encoding putative alpha/beta hydrolase fold, putative vacuolar H+ -ATPase B subunit, putative tyrosine phosphatase, were confirmed to be regulated under ABA treatment by RT-PCR and northern blot analysis. FDD-PCR and possible functional mechanisms of ABA were discussed.

Abscisic Acid↗