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人类激肽释放酶基因KLK2和KLK3内异常的可变剪接产生了新的前列腺特异性蛋白。

Unusual alternative splicing within the human kallikrein genes KLK2 and KLK3 gives rise to novel prostate-specific proteins.

作者信息

David Anat, Mabjeesh Nicola, Azar Idit, Biton Sharon, Engel Sharon, Bernstein Jeanne, Romano Jacob, Avidor Yoav, Waks Tova, Eshhar Zelig, Langer Salomon Z, Lifschitz-Mercer Beatriz, Matzkin Haim, Rotman Galit, Toporik Amir, Savitsky Kinneret, Mintz Liat

机构信息

Compugen Ltd., 72 Pinchas Rosen St., Tel Aviv 69512, Israel.

出版信息

J Biol Chem. 2002 May 17;277(20):18084-90. doi: 10.1074/jbc.M102285200. Epub 2002 Feb 7.

Abstract

Prostate-specific antigen (PSA) and human kallikrein 2 are closely related products of the human kallikrein genes KLK3 and KLK2, respectively. Both PSA and human kallikrein 2 are produced and secreted in the prostate and have important applications in the diagnosis of prostate cancer. We report here the identification of unusual mRNA splice variants of the KLK2 and KLK3 genes that result from inclusion of intronic sequences adjacent to the first exon. The novel proteins encoded by these transcripts, named PSA-linked molecule (PSA-LM) and hK2-linked molecule (K-LM), share only the signal peptide with the original protein product of the respective gene. The mature proteins are entirely different and bear no similarity to the kallikrein family or to other proteins in the databases. As is the case with PSA, PSA-LM is expressed in the secretory epithelial cells of the prostate and is up-regulated in response to androgenic stimulation. A similar pattern of expression is suggested for K-LM.

摘要

前列腺特异性抗原(PSA)和人激肽释放酶2分别是人类激肽释放酶基因KLK3和KLK2的密切相关产物。PSA和人激肽释放酶2均在前列腺中产生和分泌,并在前列腺癌的诊断中具有重要应用。我们在此报告KLK2和KLK3基因异常mRNA剪接变体的鉴定,这些变体是由于包含与第一个外显子相邻的内含子序列而产生的。由这些转录本编码的新型蛋白质,分别命名为PSA连接分子(PSA-LM)和hK2连接分子(K-LM),仅与各自基因的原始蛋白质产物共享信号肽。成熟蛋白完全不同,与激肽释放酶家族或数据库中的其他蛋白质没有相似性。与PSA一样,PSA-LM在前列腺的分泌上皮细胞中表达,并在雄激素刺激下上调。K-LM也显示出类似的表达模式。

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