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Scientists use DNA to store digital movies inside living cells (w/video)

(Nanowerk News) Researchers are developing ways to harness DNA, the blueprint of biological life, as a synthetic raw material to store large amounts of digital information outside of living cells, using expensive machinery. But what if they could coerce living cells, like large populations of bacteria, into using their own genomes as a biological hard drive that can record information that can be accessed anytime? Such an approach would not merely open entirely new possibilities of data storage but could also be engineered further into an effective memory device capable of recording, in a chronological fashion, the molecular experiences of cells as they develop or as they get exposed to stresses, such as infections and pathogens.
In 2016, a team from Harvard Medical School and the Wyss Institute for Biologically Inspired Engineering led by George Church built the first molecular recorder based on the CRISPR system that allows cells to acquire bits of chronologically provided, DNA-encoded information to generate a memory of them in the genome of bacteria as a cell model. The information, stored away as an array of sequences in the CRISPR locus can be recalled and used to reconstruct a timeline of events.
However, “as promising as this was, we did not know what would happen when we tried to track about a hundred sequences at once, or if it would work at all,” said Seth Shipman, a research fellow in genetics working with Church. “This was critical since we are aiming to use this system to record complex biological events as our ultimate goal.”
new CRISPR technology enables the recording of digital data in a population of living bacteria
The new CRISPR technology enables the recording of digital data, like those presenting successive frames of the movie of a galloping horse, one of the first made ever, in a population of living bacteria. (Image: Wyss Institute)
Now, in a study published July 12 in Nature ("CRISPR–Cas encoding of a digital movie into the genomes of a population of living bacteria"), the same team shows in proof-of-principle experiments that the CRISPR system, developed further as a first-of-its-kind approach, is able to encode in living cells information as complex as a digitized image of a human hand, reminiscent of some of the first paintings drawn on cave walls by early humans, and a sequence of one of the first motion pictures ever made, that of a galloping horse.
The CRISPR system helps bacteria fend off a constant onslaught of viruses in their different environments. As a memory of survived infections, it captures viral DNA molecules and generates short, so-called “spacer,” sequences from them that are added as new elements upstream of previous elements in a growing array located in the CRISPR locus of bacterial genomes. The CRISPR-Cas9 protein constantly resorts to this memory to destroy the same viruses when they return. Besides Cas9, which has become a widely used genome engineering tool, other parts of the CRISPR system, however, have so far not been exploited much technologically.
“In this study, we show that two proteins of the CRISPR system, Cas1 and Cas2, that we have engineered into a molecular recording tool, together with new understanding of the sequence requirements for optimal spacers, enables a significantly scaled-up potential for acquiring memories and depositing them in the genome—as information that can be provided by researchers from the outside, or that, in the future, could be formed from the cells natural experiences,” said Church, who also is the Robert Winthrop Professor of Genetics at HMS. “Harnessed further, this approach could present a way to cue different types of living cells in their natural tissue environments into recording the formative changes they are undergoing into a synthetically created memory hotspot in their genomes.”
In this video, Wyss Institute and Harvard Medical School researchers George Church and Seth Shipman explain how they engineered a new CRISPR system-based technology that enables the chronological recording of digital information, like that representing still and moving images, in living bacteria. (Video: Wyss Institute)
To approach complex information on much larger scales, the team resorted to still and moving images because they represent constrained and clearly defined data sets while a movie offers the additional opportunity to have bacteria acquire information frame-wise over time.
“We designed strategies that essentially translate the digital information contained in each pixel of an image or frame as well as the frame number into a DNA code, that, with additional sequences, is incorporated into spacers. Each frame thus becomes a collection of spacers,” said Shipman, the study’s first author. “We then provided spacer collections for consecutive frames chronologically to a population of bacteria which, using Cas1/Cas2 activity, added them to the CRISPR arrays in their genomes. And after retrieving all arrays again from the bacterial population by DNA sequencing, we finally were able to reconstruct all frames of the galloping horse movie and the order they appeared in.”
While realizing this new concept of molecular recording, Shipman, together with second-author Jeff Nivala, a research fellow in genetics at HMS, identified a valuable set of requirements in their analysis that make spacer sequences likely to be more easily acquired and defined sequence features that prevent their acquisition into growing CRISPR arrays—the dos and don’ts of spacer design.
In future work, the team will focus on establishing molecular recording devices in other cell types and on further engineering the system so that it can memorize biological information. “One day, we may be able to follow all the developmental decisions that a differentiating neuron is taking from an early stem cell to a highly specialized type of cell in the brain, leading to a better understanding of how basic biological and developmental processes are choreographed,” said Shipman, who is also mentored by neurobiologist and co-author Jeffrey Macklis, the HMS Max and Anne Wien Professor of Life Sciences and Professor of Stem Cell and Regenerative Biology at Harvard University. Once adapted to specific paradigms, the approach could also lead to better methods for generating cells for regenerative therapy, disease modeling and drug testing.
“This groundbreaking technology advances the field of DNA-based information storage by leveraging the biological machinery of living cells to record, archive and propagate that information in addition to potentially providing new way to study dynamic biological and developmental processes inside the living body. It is yet another example of bioinspired engineering at its best,” said Donald Ingber, Wyss founding director, the HMS Judah Folkman Professor of Vascular Biology in the Department of Surgery at Boston Children’s Hospital and professor of bioengineering at the Harvard John A. Paulson School of Engineering and Applied Sciences.
Source: By Benjamin Boettner, Harvard Medical School
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