Back to chapter

11.9:

Regulated mRNA Transport

JoVE Core
Cell Biology
This content is Free Access.
JoVE Core Cell Biology
Regulated mRNA Transport

Languages

Share

The transport of mRNAs from the nucleus to specific locations in the cytoplasm is a highly regulated process aided by a variety of cis- and trans-acting elements.

mRNA contains cis-acting elements at the 3’ and, less often, at the 5’ untranslated regions of the mRNA. These localization elements, also known as zip-code regions, can be up to a thousand base pairs in length and determine the cytoplasmic localization of the exported mRNA.

The trans-acting elements include mRNA binding proteins that recognize specific sequences or structures formed by the mRNA and, together with RNA, form heterogeneous nuclear ribonucleoprotein particles.  

mRNA in these particles is then exported through nuclear pore complexes with the help of exporter proteins that associate with both the mRNA and the nuclear pore complexes. 

Nucleus-specific proteins detach from the mRNA before it is exported to the cytoplasm while exporter proteins leave the mRNA in the cytoplasm and return to the nucleus for further mRNA export.

Some mRNAs are transported to a specific location as directed by their zip-code sequences before starting protein production and remain translationally inactive until they reach their target location.

The mRNAs are transported to the target location by random diffusion or with the help of cytoskeletal filaments. The mRNAs are then trapped by anchor proteins, which help them to remain at a specified location.

Free ribosomes bind to mRNA and start the process of the translation to produce proteins. If the final protein carries a target sequence for an organelle, it will be directed to the respective organelle. 

If the synthesized protein is a cell surface or secreted protein, its target peptide sequence will be recognized, and the whole complex of the mRNA, ribosome, and newly synthesized peptide will be transferred to the surface of the endoplasmic reticulum for further synthesis.

11.9:

Regulated mRNA Transport

In eukaryotes, transcription and translation are compartmentalized; an mRNA is first synthesized in the nucleus and then selectively transported to the cytoplasm for protein synthesis. Before transport, a pre-mRNA undergoes several steps of post-transcriptional modifications including splicing, 5' capping, and the addition of a poly-adenine tail. Various proteins bind to the pre-mRNA during these modifications. The mRNA transport takes place with the help of multiple proteins playing specific roles during different stages of the mRNA transport. For example, mRNA is exported through the nuclear pore complexes with the help of an exporter protein, which is a heterodimer of nuclear export factor 1 and nuclear export transporter 1. These proteins recognize specific nucleotide sequences or stem-loop structures formed by the mRNA and can bind different types of mRNA with similar binding features.

 mRNA is usually transported from the nucleus only after it is fully processed. However, some RNA from specific viruses, such as the Human Immunodeficiency Virus (HIV), can circumvent this rule.  HIV transfers some of its intron carrying pre-mRNA from the nucleus to the cytoplasm with the help of a protein called Rev. Rev is encoded by HIV RNA and binds to the specific sequences present within the pre-mRNA introns as well as the nuclear export receptor. This facilitates the transport of the intron-carrying pre-mRNA to the cytoplasm.

Cytoplasmic Fate of the transported mRNA

Once transferred into the cytoplasm, the further journey of the mRNA within the cytoplasm largely depends on whether it encodes organelle-specific, secretory, or cell surface protein. In the case of organelle-specific proteins, the protein produced will be transported to the respective organelle with the help of a signal peptide sequence. On the other hand, if a particular mRNA produces a secretory protein, the mRNA will be directed to the endoplasmic reticulum along with the associated ribosome and nascent peptide. This will happen during the initial stages of the protein synthesis, and the transferred mRNA- ribosome complex will remain on the endoplasmic reticulum until the protein synthesis is complete.

In contrast, some mRNAs are transported to specific locations in the cytoplasm before starting protein production. Such localization signals, known as zip-code regions, are present in the 3' untranslated regions of the mRNA. mRNA transport to the target location can be either random or directed by cytoskeletal filaments. Such mRNA localization not only helps cells to produce high concentrations of proteins near to the target location, but it also eliminates the need for the cell to use resources to transport the protein to its final destination.

Suggested Reading

  1. Martin, Kelsey C., and Anne Ephrussi. "mRNA localization: gene expression in the spatial dimension." Cell 136, no. 4 (2009): 719-730.
  2. Eliscovich, Carolina, Adina R. Buxbaum, Zachary B. Katz, and Robert H. Singer. "mRNA on the move: the road to its biological destiny." Journal of Biological Chemistry 288, no. 28 (2013): 20361-20368.
  3. Di Liegro, Carlo Maria, Gabriella Schiera, and Italia Di Liegro. "Regulation of mRNA transport, localization and translation in the nervous system of mammals." International Journal of Molecular Medicine 33, no. 4 (2014): 747-762.