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正常及肿瘤性卵巢、子宫内膜和子宫肌层中人类端粒酶逆转录酶(hTERT)可变剪接对端粒酶的调控

Regulation of telomerase by alternate splicing of human telomerase reverse transcriptase (hTERT) in normal and neoplastic ovary, endometrium and myometrium.

作者信息

Ulaner G A, Hu J F, Vu T H, Oruganti H, Giudice L C, Hoffman A R

机构信息

Department of Gynecology and Obstetrics, Stanford University School of Medicine, Palo Alto, CA, USA.

出版信息

Int J Cancer. 2000 Feb 1;85(3):330-5.

Abstract

Telomerase extends telomeric repeats at the ends of linear chromosomes, thereby prolonging the replicative capacity of cells. To investigate possible regulatory mechanisms of telomerase, we measured telomerase enzyme activity, human telomerase RNA (hTR) and human telomerase reverse transcriptase (hTERT) mRNA in normal and neoplastic ovary, endometrium and myometrium. Telomerase activity was detected in most malignancies and in normal endometrium but not in myometrial leiomyoma, normal myometrium or normal ovary. hTR was expressed in all tissue samples. hTERT mRNA was expressed in many tissue samples, and no tissue sample exhibited telomerase activity without expressing hTERT mRNA. However, the presence of hTR and hTERT mRNA was not sufficient for telomerase activity. Alternate splicing of hTERT produced mRNAs lacking critical reverse transcriptase (RT) motifs in both normal and neoplastic tissues. Only tissues expressing hTERT containing complete A and B RT motifs demonstrated telomerase activity. Finally, several normal ovarian tissues and myometrial leiomyomas lacked telomerase activity despite expressing hTR and hTERT containing complete A and B RT motifs. This was not seen in ovarian and myometrial malignancies, where the expression of hTR and hTERT containing complete A and B RT motifs was sufficient for telomerase activity. We conclude that in ovarian and uterine tissues, the presence of a functional telomerase complex is regulated at multiple levels, including hTERT transcription and alternative splicing of hTERT transcripts. The lack of telomerase activity in several normal but not malignant tissues expressing hTR and hTERT containing complete A and B RT motifs suggests that there are further mechanisms for suppressing telomerase activity downstream of hTERT transcription and mRNA splicing, and these mechanisms have been lost during neoplastic transformation.

摘要

端粒酶可延长线性染色体末端的端粒重复序列,从而延长细胞的复制能力。为了研究端粒酶可能的调控机制,我们检测了正常及肿瘤性卵巢、子宫内膜和子宫肌层中的端粒酶活性、人端粒酶RNA(hTR)和人端粒酶逆转录酶(hTERT)mRNA。在大多数恶性肿瘤及正常子宫内膜中检测到了端粒酶活性,但子宫肌层平滑肌瘤、正常子宫肌层或正常卵巢中未检测到。hTR在所有组织样本中均有表达。hTERT mRNA在许多组织样本中表达,且没有组织样本在不表达hTERT mRNA的情况下表现出端粒酶活性。然而,hTR和hTERT mRNA的存在并不足以产生端粒酶活性。在正常组织和肿瘤组织中,hTERT的可变剪接产生了缺乏关键逆转录酶(RT)基序的mRNA。只有表达含有完整A和B RT基序的hTERT的组织才表现出端粒酶活性。最后,尽管一些正常卵巢组织和子宫肌层平滑肌瘤表达了含有完整A和B RT基序的hTR和hTERT,但仍缺乏端粒酶活性。在卵巢和子宫肌层恶性肿瘤中未观察到这种情况,在这些肿瘤中,表达含有完整A和B RT基序的hTR和hTERT足以产生端粒酶活性。我们得出结论,在卵巢和子宫组织中,功能性端粒酶复合物的存在受到多个水平的调控,包括hTERT转录和hTERT转录本的可变剪接。在一些表达含有完整A和B RT基序的hTR和hTERT的正常但非恶性组织中缺乏端粒酶活性,这表明在hTERT转录和mRNA剪接下游存在进一步抑制端粒酶活性的机制,而这些机制在肿瘤转化过程中已经丧失。

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