コンテンツへスキップ
Merck
  • Gene make-up: rapid and massive intron gains after horizontal transfer of a bacterial α-amylase gene to Basidiomycetes.

Gene make-up: rapid and massive intron gains after horizontal transfer of a bacterial α-amylase gene to Basidiomycetes.

BMC evolutionary biology (2013-02-15)
Jean-Luc Da Lage, Manfred Binder, Aurélie Hua-Van, Stefan Janeček, Didier Casane
要旨

Increasing genome data show that introns, a hallmark of eukaryotes, already existed at a high density in the last common ancestor of extant eukaryotes. However, intron content is highly variable among species. The tempo of intron gains and losses has been irregular and several factors may explain why some genomes are intron-poor whereas other are intron-rich. We studied the dynamics of intron gains and losses in an α-amylase gene, whose product breaks down starch and other polysaccharides. It was transferred from an Actinobacterium to an ancestor of Agaricomycotina. This gene underwent further duplications in several species. The results indicate a high rate of intron insertions soon after the gene settled in the fungal genome. A number of these oldest introns, regularly scattered along the gene, remained conserved. Subsequent gains and losses were lineage dependent, with a majority of losses. Moreover, a few species exhibited a high number of both specific intron gains and losses in recent periods. There was little sequence conservation around insertion sites, then probably little information for splicing, whereas splicing sites, inside introns, showed typical and conserved patterns. There was little variation of intron size. Since most Basidiomycetes have intron-rich genomes and this richness was ancestral in Fungi, long before the transfer event, we suggest that the new gene was shaped to comply with requirements of the splicing machinery, such as short exon and intron sizes, in order to be correctly processed.

材料
製品番号
ブランド
製品内容

Sigma-Aldrich
α-アミラーゼ, 熱安定型, solution, for use in Total Dietary Fiber Assay, TDF-100A
Sigma-Aldrich
α-アミラーゼ from human saliva, Type XIII-A, lyophilized powder, 300-1,500 units/mg protein
Sigma-Aldrich
α-アミラーゼ ブタ膵臓由来, Type VI-B, ≥5 units/mg solid
Sigma-Aldrich
α-アミラーゼ from Aspergillus oryzae, powder, ~30 U/mg
Sigma-Aldrich
タカジアスターゼ from Aspergillus oryzae, powder, slightly beige, ~100 U/mg
Sigma-Aldrich
α-アミラーゼ from Aspergillus oryzae, ≥150 units/mg protein (biuret)
Sigma-Aldrich
α-アミラーゼ Bacillus licheniformis由来, Type XII-A, saline solution, ≥500 units/mg protein (biuret)
Sigma-Aldrich
α-アミラーゼ Bacillus sp.(バシラス属)由来, Type II-A, lyophilized powder, ≥1,500 units/mg protein (biuret)
Sigma-Aldrich
α-アミラーゼ from human saliva, Type IX-A, lyophilized powder, 1,000-3,000 units/mg protein
Sigma-Aldrich
α-アミラーゼ Bacillus subtilis(枯草菌)由来, powder, yellow-brown, ~50 U/mg
Sigma-Aldrich
α-アミラーゼ Bacillus licheniformis由来, lyophilized powder, 500-1,500 units/mg protein, 93-100% (SDS-PAGE)
Sigma-Aldrich
α-アミラーゼ from Aspergillus oryzae, powder, ~1.5 U/mg (~0.2 U acc. to Willstätter)
Sigma-Aldrich
α-アミラーゼ Bacillus sp.(バシラス属)由来, liquid
Sigma-Aldrich
α-アミラーゼ ブタ膵臓由来, PMSF Treated, Type I-A, saline suspension, ≥1000 units/mg protein (E1%/280)
Sigma-Aldrich
α-アミラーゼ Bacillus sp.(バシラス属)由来, powder, ≥400 units/mg protein (Lowry)
Sigma-Aldrich
α-アミラーゼ from Aspergillus oryzae, aqueous solution, ≥800 FAU/g
Sigma-Aldrich
α-アミラーゼ Bacillus amyloliquefaciens由来, liquid, ≥250 units/g
Sigma-Aldrich
α-アミラーゼ Bacillus subtilis(枯草菌)由来, powder, yellow-brown, ~380 U/mg
Sigma-Aldrich
α-アミラーゼ ブタ膵臓由来, Type I-A, PMSF treated, saline suspension, 700-1400 units/mg protein (E1%/280)
Supelco
α-アミラーゼ Bacillus licheniformis由来, suitable for determination of starch (Kit STA-20)