Liu X F, Olsson P, Wolfgang C D, Bera T K, Duray P, Lee B, Pastan I
Laboratory of Molecular Biology, Division of Basic Sciences, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
Prostate. 2001 May 1;47(2):125-31. doi: 10.1002/pros.1055.
The database of human Expressed Sequence Tags (dbEST) provides a potential source for identification of tissue-specific genes. This database contains sequences that originate from cDNA libraries from particular tumors, organs or cell types. In this report, we have used the EST database to identify PRAC, a novel gene specifically expressed in human Prostate, prostate cancer, Rectum And distal Colon.
Using a computer based analysis, a cluster of sequence homologous ESTs was identified which contained ESTs derived only from human prostate cDNA libraries. The tissue specificity was examined by multiple tissue RNA dot blots and RT-PCR. The PRAC transcript and protein was identified using Northern blot analysis, RACE-PCR, primer extension, and western blot.
PRAC encode a 382 nucleotide RNA found in prostate, rectum, distal colon, and in three prostate cancer cell lines; LNCaP, PC-3 and DU145. This transcript encodes a 6 kDa nuclear protein. The PRAC gene is located on chromosome 17 at position 17q21, about 4 kbp downstream from the homeodomain Hoxb-13 gene.
Our data proves that the EST database can be a useful tool for discovery of prostate-specific genes. The nuclear localization, identification of potential phosphorylation sites, and possible cotranscription with the Hoxb-13 gene suggest that PRAC may have a regulatory role in the nucleus.
人类表达序列标签数据库(dbEST)为鉴定组织特异性基因提供了一个潜在来源。该数据库包含源自特定肿瘤、器官或细胞类型的cDNA文库的序列。在本报告中,我们利用EST数据库鉴定了PRAC,这是一种在人类前列腺、前列腺癌、直肠和远端结肠中特异性表达的新基因。
通过基于计算机的分析,鉴定出一组序列同源的ESTs,其中仅包含源自人类前列腺cDNA文库的ESTs。通过多重组织RNA斑点印迹和RT-PCR检测组织特异性。使用Northern印迹分析、RACE-PCR、引物延伸和蛋白质印迹鉴定PRAC转录本和蛋白质。
PRAC编码一种在前列腺、直肠、远端结肠以及三种前列腺癌细胞系(LNCaP、PC-3和DU145)中发现的382个核苷酸的RNA。该转录本编码一种6 kDa的核蛋白。PRAC基因位于17号染色体上17q21位置,在同源异型域Hoxb-13基因下游约4 kbp处。
我们的数据证明EST数据库可成为发现前列腺特异性基因的有用工具。核定位、潜在磷酸化位点的鉴定以及与Hoxb-13基因可能的共转录表明PRAC可能在细胞核中具有调节作用。