DropSynth can make thousands of genes at once for just a few dollars apiece
A new technique pioneered by UCLA researchers could enable scientists in any typical biochemistry laboratory to make their own gene sequences for only about $2 per gene. Researchers now generally buy gene sequences from commercial vendors for $50 to $100 per gene.
The approach, DropSynth, which is described in the January issue of the journal Science, makes it possible to produce thousands of genes at once. Scientists use gene sequences to screen for gene’s roles in diseases and important biological processes.
“Our method gives any lab that wants the power to build its own DNA sequences,” said Sriram Kosuri, a UCLA assistant professor of chemistry and biochemistry and senior author of the study. “This is the first time that, without a million dollars, an average lab can make 10,000 genes from scratch.”
Increasingly, scientists studying a wide range of subjects in medicine — from antibiotic resistance to cancer — are conducting “high-throughput” experiments, meaning that they simultaneously screen hundreds or thousands of groups of cells. Analyzing large numbers of cells, each with slight differences in their DNA, for their ability to carry out a behavior or survive a drug treatment can reveal the importance of particular genes, or sections of genes, in those abilities.
Such experiments require not only large numbers of genes but also that those genes are sequenced. Over the past 10 years, advances in sequencing have enabled researchers to simultaneously determine the sequences of many strands of DNA. So the cost of sequencing has plummeted, even as the process of generating genes has remained comparatively slow and expensive.
“There’s an ongoing need to develop new gene synthesis techniques,” said Calin Plesa, a UCLA postdoctoral research fellow and co-first author of the paper. “The more DNA you can synthesize, the more hypotheses you can test.”
The current methods for synthesizing genes, he said, either limit the length of a gene to about 200 base pairs — the sets of nucleotides that made up DNA — or are prohibitively expensive for most labs.
The new method involves isolating small sections of thousands of genes in tiny droplets of water suspended in an oil. Each section of DNA is assigned a molecular “bar code,” which identifies the longer gene to which it belongs.
Then, the sections, which initially are present in only very small amounts, are copied many times to increase their number. Finally, small beads are used to sort the mixture of DNA fragments into the right combinations to make longer genes, and the sections are combined. The result is a mixture of thousands of the desired genes, which can be used in experiments.
To show that technique worked, the scientists used DropSynth to make thousands of bacterial genes — each as long as 669 base pairs in length. Each gene encoded a different bacterium’s version of the metabolic protein phosphopantetheine adenylyltransferase, or PPAT, which bacteria need to survive. Because PPAT is critical to bacteria that cause everything from sinus infections to pneumonia and food poisoning, it’s being studied as a potential antibiotic target.
The researchers created a mixture of the thousands of versions of PPAT with DropSynth, and then added each gene to a version of E. coli that lacked PPAT and tested which ones allowed E. coli to survive. The surviving cells could then be used to screen potential antibiotics very quickly and at a low cost.
DropSynth could potentially also be useful in engineering new proteins. Currently, scientists can use computer programs to design proteins that meet certain parameters, such as the ability to bind to certain molecules, but DropSynth could offer researchers hundreds or even thousands of options from which to choose the proteins that best fit their needs.
The team is still working on reducing DropSynth’s error rate. In the meantime, though, the scientists have made the instructions publicly available on their website. All of the chemical substances needed to replicate the approach are commercially available.
Learn more: UCLA scientists develop low-cost way to build gene sequences
The Latest on: Gene sequencing
[google_news title=”” keyword=”gene sequencing” num_posts=”10″ blurb_length=”0″ show_thumb=”left”]
via Google News
The Latest on: Gene sequencing
- Genetic Disorders Diagnosed More Quickly via Long-Read Sequencing Methodon July 24, 2024 at 9:34 am
Researchers claim NanoRanger shows paradigm-shifting reliability in resolving disease-causing breakpoints that are missed by conventional clinical testing.
- deCODE Study Uncovers Link Between Genomic Variants and DNA Methylationon July 24, 2024 at 7:10 am
One of the advantages of sequencing DNA using nanopores—technology commercialized by ONT (Oxford Nanopore Technology)—is that it allows for DNA sequence analysis in real-time. Not only that, but it ...
- The Power Of Role Models In Deep Tech: Inspiring The Next Generationon July 24, 2024 at 5:45 am
By bridging the gap between inspiration and execution, we can build a thriving tech ecosystem that addresses the challenges of our time.
- Next Generation Sequencing Market to Witness 18.5% CAGR by 2031 | SkyQuest Technologyon July 24, 2024 at 5:29 am
SkyQuest projects that Next Generation Sequencing Market will attain a value of USD 36.04 billion by 2031, with a CAGR of 18.5% during the forecast period (2024-2031). Next generation sequencing is a ...
- New RNA Sequencing Dataset Reveals Genetic Diversity Across Global Populationson July 24, 2024 at 4:38 am
An open-access dataset of RNA sequences from lymphoblastoid cell lines of 731 individuals spanning 26 populations and five continental groups.
- With the U.S. bird flu outbreak uncontained, scientists see growing riskson July 24, 2024 at 3:01 am
A recent crop of human cases at a chicken farm highlight the risks of the ongoing outbreak. Here's what scientists fear could happen next in the evolution of the virus.
- deCODE genetics: Variants in the genome affect DNA methylationon July 24, 2024 at 2:25 am
A new study by scientists at deCODE Genetics, subsidiary of Amgen, shows that sequence variants drive the correlation between DNA methylation and gene expression. The same variants are linked to ...
- Study links sequence variants to DNA methylation and diseaseson July 24, 2024 at 2:00 am
A new study by scientists at deCODE Genetics shows that sequence variants drive the correlation between DNA methylation and gene expression. The same variants are linked to various diseases and other ...
- Sequencing technique searches for complex genomic variants to provide accurate diagnosis within hourson July 23, 2024 at 8:00 am
Despite rapid advances in genetic testing in recent decades, more than half of people worldwide with suspected Mendelian genetic disorders do not have an accurate molecular diagnosis. Others endure ...
via Bing News