生物
核糖核蛋白
计算生物学
遗传学
基因
基因表达调控
HEK 293细胞
非编码RNA
基因表达
长非编码RNA
核糖核酸
机制(生物学)
编码
RNA干扰
人类基因组
电池类型
细胞生物学
剂量补偿
进化生物学
翻译(生物学)
基因剔除小鼠
功能(生物学)
模式生物
基因调控网络
基因表达谱
RNA结合蛋白
细胞
作者
Wayne O. Hemphill,Arthur J. Zaug,Cody J.S. Hecht,Thomas R. Cech
出处
期刊:RNA
[Cold Spring Harbor Laboratory Press]
日期:2026-07-30
卷期号:32 (10): 1643-1662
被引量:1
标识
DOI:10.1261/rna.081170.126
摘要
ABSTRACT In 1986, a class of small, noncoding RNAs was discovered in association with an enormous, enigmatic ribonucleoprotein complex – the “vault” particle – and thus dubbed vault RNAs (vtRNAs). However, it’s since been recognized that the vast majority (≥95%) of these noncoding vtRNA molecules are not associated with the mysterious vaults, raising questions about their potential independent function(s). Moreover, humans express four vtRNAs from two different loci, and debate has arisen about whether the vtRNA paralogs share any functional connection, and whether they should remain classified together. Herein, we report the expression patterns of the four VTRNA paralogs in a variety of human cell lines, including various single- and multi-gene VTRNA -knockout cell lines. Knockout of one or more of the three VTRNA1 genes leads to increased expression of vtRNA2-1, suggesting that their biological functions are related. Additionally, we interrogated the effects of vtRNA knockout on HEK293T cell growth, viability, and viral infection, and were unable to replicate previously reported associations. Collectively, our findings point to a potential functional connection between even the most distantly related human vtRNA paralogs, while reaffirming that their biological roles and mechanisms still require critical study.
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