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Eichhorn, S. W.

Publications and source records attributed to Eichhorn, S. W..

2 recordsLinked to original sources

MicroRNAs Cause Accelerated Decay of Short-Tailed Target mRNAs

MicroRNAs (miRNAs) specify recruitment of deadenylases to mRNA targets. Despite this recruitment, we find that miRNAs have almost no effect on steady-state poly(A)-tail lengths of their targets in mouse fibroblasts, which motivates acquisition of pre-steady-state measurements of the effects of miRNAs on tail lengths, mRNA levels, and translational efficiencies. Effects on translational efficiency are minimal compared to effects on mRNA levels--even for newly transcribed target mRNAs. Effects on target mRNA levels accumulate as the mRNA population approaches steady state, whereas effects on tail lengths peak for recently transcribed target mRNAs and then subside. Computational modeling of this phenomenon reveals that miRNAs cause not only accelerated deadenylation of their targets but also accelerated decay of short-tailed target molecules. This unanticipated effect of miRNAs largely prevents short-tailed target mRNAs from accumulating despite accelerated target deadenylation. The net result is a nearly imperceptible change to the steady-state tail-length distribution of targeted mRNAs.\n\nHighlightsO_LImiRNAs cause accelerated decay of short-tailed target molecules\nC_LIO_LIThis accelerated decay largely prevents accumulation of short-tailed target mRNAs\nC_LIO_LImiRNAs are similarly effective on short-lived and long-lived target mRNAs\nC_LIO_LIIn 3T3 cells, miRNA effects on translation are negligible--even for nascent mRNA\nC_LI

genomics

The Dynamics of Cytoplasmic mRNA Metabolism

For all but a few mRNAs, the dynamics of metabolism are unknown. Here, we developed an experimental and analytical framework for examining these dynamics for mRNAs from thousands of genes. mRNAs of mouse fibroblasts exit the nucleus with diverse intragenic and intergenic poly(A)-tail lengths. Once in the cytoplasm, they have a broad (1000-fold) range of deadenylation rate constants, which correspond to cytoplasmic lifetimes. Indeed, with few exceptions, degradation appears to occur primarily through deadenylation-linked mechanisms, with little contribution from either endonucleolytic cleavage or deadenylation-independent decapping. Most mRNA molecules degrade only after their tail lengths fall below 25 nt. Decay rate constants of short-tailed mRNAs vary broadly (1000-fold) and are more rapid for short-tailed mRNAs that had previously undergone more rapid deadenylation. This coupling helps clear rapidly deadenylated mRNAs, enabling the large range in deadenylation rate constants to impart a similarly large range in stabilities.\n\nHighlightsO_LImRNAs enter the cytoplasm with diverse intra- and intergenic lengths\nC_LIO_LImRNA deadenylation rates span a 1000-fold range and correspond to mRNA half-lives\nC_LIO_LIAfter their tails become short, mRNAs decay at rates that span a 1000-fold range\nC_LIO_LIMore rapidly deadenylated mRNAs decay more rapidly upon reaching short tail lengths\nC_LI

genomics