Engineering an <scp>RNA</scp>/protein‐binding module for higher transgene protein production and improved long‐term durability

Yu‐Hung Hung(Donald Danforth Plant Science Center), Eric T. Wang(Donald Danforth Plant Science Center), Tayahna Agtarap(Donald Danforth Plant Science Center), Gerald Klaas(Donald Danforth Plant Science Center), R. Keith Slotkin(Donald Danforth Plant Science Center)
The Plant Journal
June 1, 2025
Cited by 1Open Access
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Abstract

Improvement and research of plants depends on the long-term expression of transgenes. However, the durability of transgene expression is routinely hampered by silencing pathways that start as the post-transcriptional process of mRNA degradation by RNA interference (RNAi). To avoid transgene silencing, we aimed to inhibit the sorting of transgene mRNAs into RNAi. We manipulated a well-studied protein/RNA-binding module from Arabidopsis into a transgene transcript, where the transcript is now bound by an engineered RNA-binding protein that preferentially sorts the RNA into translation. We used the Cas9 transcript as a proof-of-principle and demonstrated higher Cas9 protein production and gene editing rates. In addition, transgenes with the engineered protein/RNA-binding module had improved long-term durability of transgene expression, as after several inbred generations these plants had higher Cas9 protein accumulation and lower levels of DNA methylation, a hallmark of transgene silencing. Our engineered system represents a successful manipulation of post-transcriptional RNA sorting for improved transgene performance, and could be applied to any transgene transcript.


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