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帚尾袋貂(Trichosurus vulpecula)干细胞因子(c-kit配体)cDNA的克隆、测序及表达

Cloning, sequencing and expression of stem cell factor (c-kit ligand) cDNA of brushtail possum (Trichosurus vulpecula).

作者信息

Greenwood P J, Seamer C, Tisdall D J

机构信息

AgResearch, Wallaceville Animal Research Centre, Upper Hutt, New Zealand.

出版信息

Reprod Fertil Dev. 1996;8(4):789-95. doi: 10.1071/rd9960789.

Abstract

By means of reverse transcription polymerase chain reaction (RT-PCR), three stem cell factor (SCF) cDNAs (822-738 bp in size) were amplified from brushtail possum ovarian poly (A)+ RNA. The largest and smallest of these cDNAs were cloned and sequenced. Characterization of these cDNAs has revealed that possum SCF has approximately 75% and 66% homology to SCF of eutherian mammals at the nucleotide level and the predicted amino acid level respectively. Nucleotide sequencing shows that the 738-bp cDNA represents an mRNA splice variant, equivalent to that found in eutherian mammals, in which an exon (84 bp) encoding a potential proteolytic cleavage site is removed. Comparison of the predicted possum SCF amino acid sequence with the predicted SCF amino acid sequences from eutherian mammals reveals conservation of all cysteine residues and 3 of 4 potential N-linked glycosylation sites. In addition, the hydropathicity profile of the possum SCF protein is similar to that of eutherian SCF suggesting that protein conformation is conserved. Northern analysis was used to characterize possum SCF gene expression in adult ovary and testis. A major transcript of 9 kb was observed in both ovarian and testicular tissue. The conservation of the SCF gene and its predicted protein, suggests that SCF in the possum has similar biological activities to SCF in eutherian mammals.

摘要

通过逆转录聚合酶链反应(RT-PCR),从帚尾袋貂卵巢聚腺苷酸加尾RNA(poly(A)+ RNA)中扩增出3个干细胞因子(SCF)cDNA(大小为822 - 738 bp)。对其中最大和最小的cDNA进行了克隆和测序。这些cDNA的特征表明,袋貂SCF在核苷酸水平和预测的氨基酸水平上分别与真兽类哺乳动物的SCF具有约75%和66%的同源性。核苷酸测序表明,738 bp的cDNA代表一种mRNA剪接变体,等同于在真兽类哺乳动物中发现的变体,其中一个编码潜在蛋白水解切割位点的外显子(84 bp)被去除。将预测的袋貂SCF氨基酸序列与真兽类哺乳动物预测的SCF氨基酸序列进行比较,发现所有半胱氨酸残基以及4个潜在的N-连接糖基化位点中的3个是保守的。此外,袋貂SCF蛋白的亲水性图谱与真兽类SCF相似,表明蛋白质构象是保守的。采用Northern印迹分析来表征袋貂SCF基因在成年卵巢和睾丸中的表达。在卵巢和睾丸组织中均观察到一个9 kb的主要转录本。SCF基因及其预测蛋白的保守性表明,袋貂中的SCF与真兽类哺乳动物中的SCF具有相似的生物学活性。

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