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解旋酶无法弥补[具体生物体]中Prp43p的缺失。 (你提供的原文“in.”后面缺少具体信息,这里是补充完整后的译文示意)

helicase fails to complement loss of Prp43p in .

作者信息

Karpel Jonathan E

机构信息

Biology, Southern Utah University, Cedar City, Utah, United States.

出版信息

MicroPubl Biol. 2024 Jan 22;2024. doi: 10.17912/micropub.biology.001113. eCollection 2024.

Abstract

Helicase proteins have important roles in many aspects of RNA metabolism in the cell. The function of these highly conserved proteins is commonly preserved between organisms, yet in a few cases these homologues are found to have slightly different biochemical functions. Prp43 is a protein with varied roles in yeast, but here we show that the homologue of this protein is unable to rescue the loss of Prp43p. By employing a transcriptional repression experiment, the expression of DDX-15 protein in yeast is not enough to complement the loss of Prp43p, which is a yeast essential protein.

摘要

解旋酶蛋白在细胞RNA代谢的许多方面都发挥着重要作用。这些高度保守的蛋白质的功能在生物体之间通常是保守的,但在少数情况下,发现这些同源物具有略有不同的生化功能。Prp43是一种在酵母中具有多种作用的蛋白质,但我们在此表明,该蛋白质的同源物无法挽救Prp43p的缺失。通过进行转录抑制实验,酵母中DDX - 15蛋白的表达不足以弥补Prp43p的缺失,Prp43p是酵母中的一种必需蛋白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/536e/10853815/fbecc6c05f6d/25789430-2024-micropub.biology.001113.jpg

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