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担子菌灰盖鬼伞A交配型中两个b1等位基因的比较。

Comparison of two b1 alleles from within the A mating-type of the basidiomycete Coprinus cinereus.

作者信息

Gieser P T, May G

机构信息

Department of Plant Biology, University of Minnesota, St. Paul 55108-1095.

出版信息

Gene. 1994 Sep 2;146(2):167-76. doi: 10.1016/0378-1119(94)90289-5.

Abstract

We cloned and sequenced the b1 specificity gene, b1-2, from the A43 mating-type locus of the basidiomycete Coprinus cinereus, to compare its molecular structure to a previously published allele. The b1-2 gene was identified and isolated using a transformation assay for A-activity. The nucleotide (nt) sequence was determined and compared to the published sequence for the b1 specificity gene of the A42 mating-type locus. Both genes map to the same physical location within the A mating-type locus and conserved structural organization is observed at both the genomic and the protein level. Sequence alignments show that the two alleles share 73% overall nt sequence identity for the open reading frames (ORFs) and 68% overall amino acid (aa) sequence identity for the deduced polypeptides. Allowing for conservative substitutions, the overall aa sequence similarity is 79%. Comparison of the deduced aa sequences reveals several conserved structural motifs, including a DNA-binding homeodomain, putative bipartite nuclear localization signal sequences, and four predicted dimerization motifs. Regions rich in Pro and hydroxylated aa (Ser and Thr) are also common to both alleles. Sequence similarity varies greatly along the length of the gene at both the nt and aa levels. In general, similarity increases progressively from the N- to the C-terminal end with variable patterns of similarity observed for individual exons and the predicted motifs they encode. The low sequence similarity observed in the N terminus suggests that variability in this region may be involved in non-self recognition. Differing levels of positional and compositional constraint are apparent for different functional domains.

摘要

我们从担子菌灰盖鬼伞的A43交配型位点克隆并测序了b1特异性基因b1 - 2,以将其分子结构与先前发表的一个等位基因进行比较。通过A活性的转化分析鉴定并分离了b1 - 2基因。测定了核苷酸(nt)序列,并与A42交配型位点的b1特异性基因的已发表序列进行比较。这两个基因都定位于A交配型位点内的同一物理位置,并且在基因组和蛋白质水平都观察到了保守的结构组织。序列比对表明,这两个等位基因的开放阅读框(ORF)的总体核苷酸序列同一性为73%,推导的多肽的总体氨基酸(aa)序列同一性为68%。考虑到保守替换,总体氨基酸序列相似性为79%。对推导的氨基酸序列的比较揭示了几个保守的结构基序,包括一个DNA结合同源结构域、假定的双分型核定位信号序列以及四个预测的二聚化基序。富含脯氨酸和羟基化氨基酸(丝氨酸和苏氨酸)的区域在两个等位基因中也很常见。在核苷酸和氨基酸水平上,序列相似性沿基因长度变化很大。一般来说,相似性从N端到C端逐渐增加,各个外显子及其编码的预测基序呈现出不同的相似性模式。在N端观察到的低序列相似性表明该区域的变异性可能参与非自我识别。不同功能域的位置和组成约束水平明显不同。

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