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Lost in translation?

Not when it comes to control of gene expression during Drosophila development

2014-05-29
(Press-News.org) CAMBRIDGE, Mass. (May 29, 2014) – In any animal's lifecycle, the shift from egg cell to embryo is a critical juncture. This transition represents the formal initiation of development—a remarkably dynamic process that ultimately transforms a differentiated, committed oocyte to a totipotent cell capable of giving rise to any cell type in the body.

Induction of totipotency (as well as the pluripotency characteristic of embryonic stem cells) requires dramatic changes in gene expression. To date, investigations of such changes have largely focused on transcription, when DNA strands are copied into the messenger RNA (mRNA) that is subsequently translated to produce the proteins essential for proper cellular function. Yet, as Whitehead Institute Member Terry Orr-Weaver is quick to remind, at this crucial moment in life, transcription is absent.

"At the start of development, there are mechanisms other than transcription for restoring potency." Orr-Weaver says. "There are massive changes in translation accompanying the onset of development."

Recognizing the importance of translation, Orr-Weaver and her lab set out to document these "massive changes"—and their regulators—in what would be an equally massive, nearly four-year undertaking. The lab conducted perhaps the most comprehensive look yet at changes in translation and protein synthesis during a developmental change, using the oocyte-to-embryo transition in Drosophila as a model system. En route, the researchers, whose results are reported this week in the journal Cell Reports, deployed three sophisticated analytical techniques: global polysome profiling to measure active translation for thousands of mRNAs; ribosome footprint profiling to determine how efficiently each mRNA is being translated; and quantitative mass spectrometry to measure changes in protein levels at the oocyte-to-embryo transition.

"This is the first time all three pieces have been put together," Orr-Weaver says. "This comprehensive approach was crucial for gathering the insights we did."

Among those insights is the surprisingly large number of mRNAs that are translationally regulated. Approximately one thousand mRNAs were found to be upregulated, with several hundred more downregulated during this transition. Another surprise is the emergence of the protein kinase complex known as PNG as a major regulator of the observed translational changes. In earlier work, the Orr-Weaver lab had shown that the PNG kinase is necessary for the initiation of mitosis in a fertilized embryo (as opposed to the meiosis that occurs in oocytes prior to egg activation) by promoting the synthesis of Cyclin B, which is required for entry into mitosis. Subsequent work suggested that the PNG kinase's regulatory effects might be limited to activating translation of a small number of targets. This latest research, however, finds PNG acting globally, affecting translation both positively and negatively.

"For me this was unexpected," says Iva Kronja, a postdoctoral researcher in the Orr-Weaver lab and first author of the Cell Reports paper. "We knew of three mRNAs that were regulated by PNG, but these results suggest that at the oocyte-to-embryo transition, PNG controls translational status of at least 60% of translationally activated and perhaps 70% of translationally inhibited mRNAs."

Both Kronja and Orr-Weaver say this key finding shows the value of studying translation globally to record what is referred to as the "translatome". Yet the translatome provides only part of the picture. The rest is revealed through quantitative analysis of changes in the protein levels that shape the proteome. Here, too, a few surprises emerged.

The scientists discovered a set of roughly 60 mRNAs whose translation was upregulated without a corresponding increase in the levels of protein produced. This apparent paradox suggests that at the oocyte-to-embryo transition, protein degradation is occurring simultaneously with translational activation. Such compensation could maintain overall protein levels while "resetting" the proteome at restoration of totipotency, delivering proteins in a form that is optimal for embryogenesis. Kronja believes there's a quality-control aspect to this balancing act.

"I see this process as preparation for a dynamic and intense period of development," says Kronja. "Its purpose may be making sure that the right components with the right modifications are in place for embryonic development."

Orr-Weaver notes that this latest work has opened a number of new research avenues for her lab, including trying to determine whether previously unidentified proteins are regulating the switch from meiosis to mitosis at this key transitional moment.

"We found new proteins whose function has been unknown," says Orr-Weaver. "But from the dynamic changes in their levels that we observed, they may be candidates that are responsible for flipping that switch."

INFORMATION: This work was supported by the National Institutes of Health (grant GM39341), the American Cancer Society, and the Alexander von Humboldt Foundation.

Written by Matt Fearer

Terry Orr-Weaver's primary affiliation is with Whitehead Institute for Biomedical Research, where her laboratory is located and all her research is conducted. She is also an American Cancer Society Research Professor of biology at Massachusetts Institute of Technology.

Full Citation:

"Widespread changes in the posttranscriptional landscape at the Drosophila oocyte-to-embryo transition"

Cell Reports, May 29, 2014

Iva Kronja (1), Bingbing Yuan (1), Stephen Eichhorn (1,2,3), Kristina Dzeyk (4), Jeroen Krijgsveld (4), David P. Bartel (1,2,3), and Terry L. Orr-Weaver (1,2)

1. Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, MA 02142, USA

2. Department of Biology, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02142, USA

3. Howard Hughes Medical Institute, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02142, USA

4. European Molecular Biology Laboratory, 69117 Heidelberg, Germany


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[Press-News.org] Lost in translation?
Not when it comes to control of gene expression during Drosophila development