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异位 miR-975 诱导果蝇 CTP 合成酶定向细胞增殖和分化。

Ectopic miR-975 induces CTP synthase directed cell proliferation and differentiation in Drosophila melanogaster.

机构信息

School of Biological Sciences, Universiti Sains Malaysia, 11800, Penang, Malaysia.

出版信息

Sci Rep. 2019 Apr 15;9(1):6096. doi: 10.1038/s41598-019-42369-6.

Abstract

CTP synthase (CTPSyn) is an essential metabolic enzyme, synthesizing precursors required for nucleotides and phospholipids production. Previous studies have also shown that CTPSyn is elevated in various cancers. In many organisms, CTPSyn compartmentalizes into filaments called cytoophidia. In Drosophila melanogaster, only its isoform C (CTPSynIsoC) forms cytoophidia. In the fruit fly's testis, cytoophidia are normally seen in the transit amplification regions close to its apical tip, where the stem-cell niche is located, and development is at its most rapid. Here, we report that CTPSynIsoC overexpression causes the lengthening of cytoophidia throughout the entirety of the testicular body. A bulging apical tip is found in approximately 34% of males overexpressing CTPSynIsoC. Immunostaining shows that this bulged phenotype is most likely due to increased numbers of both germline cells and spermatocytes. Through a microRNA (miRNA) overexpression screen, we found that ectopic miR-975 concurrently increases both the expression levels of CTPSyn and the length of its cytoophidia. The bulging testes phenotype was also recovered at a penetration of approximately 20%. However, qPCR assays reveal that CTPSynIsoC and miR-975 overexpression each provokes a differential response in expression of a number of cancer-related genes, indicating that the shared CTPSyn upregulation seen in either case is likely the cause of observed testicular overgrowth. This study presents the first instance of consequences of miRNA-asserted regulation upon CTPSyn in D. melanogaster, and further reaffirms the enzyme's close ties to germline cells overgrowth.

摘要

CTP 合酶(CTPSyn)是一种必需的代谢酶,合成核苷酸和磷脂生成所需的前体。先前的研究还表明,CTPSyn 在各种癌症中升高。在许多生物体中,CTPSyn 分隔成称为细胞丝状伪足的纤维。在黑腹果蝇中,只有其同工型 C(CTPSynIsoC)形成细胞丝状伪足。在果蝇的睾丸中,细胞丝状伪足通常出现在靠近顶端的过渡扩增区域,干细胞龛位位于此处,且发育速度最快。在这里,我们报告说 CTPSynIsoC 的过表达导致整个睾丸体的细胞丝状伪足延长。在大约 34%过表达 CTPSynIsoC 的雄性中发现了凸起的顶端。免疫染色显示,这种凸起表型很可能是由于生殖细胞和精母细胞数量的增加。通过 miRNA(miRNA)过表达筛选,我们发现异位 miR-975 同时增加了 CTPSyn 的表达水平及其细胞丝状伪足的长度。凸起的睾丸表型也在大约 20%的穿透率下得到恢复。然而,qPCR 检测表明,CTPSynIsoC 和 miR-975 的过表达分别在一些癌症相关基因的表达中引起了不同的反应,表明在这两种情况下观察到的共同的 CTPSyn 上调很可能是观察到的睾丸过度生长的原因。本研究首次展示了 miRNA 在果蝇中对 CTPSyn 的调节作用的后果,进一步证实了该酶与生殖细胞过度生长的密切关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa15/6465261/6094dfeeeba7/41598_2019_42369_Fig1_HTML.jpg

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