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紫花苜蓿(Medicago sativa L.)体细胞胚胎发生相关cDNA的特征分析。

Characterization of somatic embryogenesis-related cDNAs from alfalfa (Medicago sativa L.).

作者信息

Giroux R W, Pauls K P

机构信息

Crop Science Department, University of Guelph, Ontario, Canada.

出版信息

Plant Mol Biol. 1997 Feb;33(3):393-404. doi: 10.1023/a:1005786826672.

Abstract

Messenger RNAs from cultures of embryogenic and non-embryogenic alfalfa (Medicago sativa L.) genotypes were used to differentially screen a cDNA library prepared from embryogenic cell masses of somatic embryo cultures to identify early-stage embryo transcripts. The three alfalfa somatic embryogenesis-specific transcripts cDNAs (ASET1, ASET2 and ASET3) identified by this screen were enriched in RNA samples from embryogenic tissues of the embryogenic genotype but were absent from petioles or mature embryos of an embryogenic genotype as well from tissue cultures of a nonembryogenic genotype. The ASET clones did not cross-hybridize and showed different patterns of expression in northerns of RNA from various fractions of alfalfa somatic embryo cultures. The ASET clones did not hybridize with the soybean embryogenesis-specific clone (Sbh1) which was shown to be expressed in embryogenic and non-embryogenic alfalfa tissue cultures. Sequencing showed ASET1 to be a partial transcript 595 nucleotides long. ASET2 was a complete transcript of 1193 nucleotides. From a comparison of the predicted open reading frame with the GenBank protein database it was concluded that ASET2 was a novel transcript. The protein predicted by the ASET2 sequence has several potential membrane-spanning domains and a potential phosphorylation site. In addition, the ASET2 cDNA had a long 5' region that contained two upstream reading frames (URFs) which could potentially code for 30 and 6 amino acid polypeptides.

摘要

来自胚性和非胚性苜蓿(紫花苜蓿)基因型培养物的信使核糖核酸被用于差异筛选一个从体细胞胚胎培养物的胚性细胞团制备的cDNA文库,以鉴定早期胚胎转录本。通过该筛选鉴定出的三个苜蓿体细胞胚胎发生特异性转录本cDNA(ASET1、ASET2和ASET3)在胚性基因型的胚性组织的RNA样本中富集,但在胚性基因型的叶柄或成熟胚胎中不存在,在非胚性基因型的组织培养物中也不存在。ASET克隆不发生交叉杂交,并且在苜蓿体细胞胚胎培养物的各个部分的RNA的Northern杂交中显示出不同的表达模式。ASET克隆不与大豆胚胎发生特异性克隆(Sbh1)杂交,Sbh1已被证明在胚性和非胚性苜蓿组织培养物中表达。测序显示ASET1是一个长度为595个核苷酸的部分转录本。ASET2是一个1193个核苷酸的完整转录本。通过将预测的开放阅读框与GenBank蛋白质数据库进行比较,得出结论ASET2是一个新的转录本。由ASET2序列预测的蛋白质具有几个潜在的跨膜结构域和一个潜在的磷酸化位点。此外,ASET2 cDNA有一个长的5'区域,其中包含两个上游阅读框(URF),它们可能编码30和6个氨基酸的多肽。

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