The TCE is distinct from the mRNA localization element.
(A) Diagram of the constructs used to map the TCE. The
SP6 promoter, 5′ UTR (shaded), coding region (hatched), 3′ UTR (black),
localization element (LE), poly(A)20 tail (white), and
relevant restriction sites are indicated on the Prl-Vg1 construct. Prl,
Prl-C2, Prl-C3, and Prl-C8 have deletions from SpeI to
EcoRI, BsmI to EcoRI,
SpeI to BsmI, and BsmI to
NsiI, respectively, as diagrammed. Prl-C7 contains two
deletions, from SpeI to BsmI and from
NsiI to EcoRI. (B) The
relative translational efficiencies of the constructs diagrammed in
A were determined (at the RNA concentration of 20 nM) as
described in Fig. 1. Values are the average of at least three
measurements; standard errors are indicated by the error bars.