\n <\/p>\n
CRISPR gene editing has made its way into every corner of modern biology, but not into every corner of the cell. Although researchers have used these systems to develop treatments for sickle-cell anaemia and blood cancers, to unlock the secrets of multicellularity and to discover the role of thousands of overlooked proteins, there\u2019s one place CRISPR can\u2019t easily reach: mitochondria.<\/p>\n
Cancer cells get power boost by stealing mitochondria from nerves<\/p>\n<\/p>\n
The rings of DNA inside mitochondria are inaccessible to these techniques, which means that precise edits to mitochondrial DNA (mtDNA) remain frustratingly out of reach. \u201cMitochondria missed the CRISPR\u2013Cas9 revolution that exploded 12 years ago,\u201d says Michal Minczuk, a geneticist at the University of Cambridge, UK.<\/p>\n
But researchers are eager to access this DNA, says Minczuk. Mitochondria are bean-shaped organelles that power cells and have myriad other cellular tasks. Exploring their DNA is essential for understanding the energy production and exchange that underlies metabolic health. And more than 300 mutations in this DNA cause mitochondrial diseases \u2014 incurable genetic disorders with a wide range of symptoms that can rob people of their sight and hearing, trigger muscle problems and spark seizures1. These disorders affect roughly 1 in 5,000 people.<\/p>\n
Because CRISPR can\u2019t help with these problems, researchers have been looking for other ways to precisely edit the mitochrondrial genome. And the past few years have brought some success: the tools are already proving to be a boon for creating accurate animal models of mitochondrial diseases. \u201cThe progress has been remarkable,\u201d says Jin-Soo Kim, a chemical biologist who develops mtDNA editing tools at the Korea Advanced Institute of Science and Technology in Daejeon, South Korea.<\/p>\n
If researchers can make mtDNA editing safe and accurate enough, it could eventually be used to treat, and even cure, these genetic conditions. \u201cIt would be a medical breakthrough,\u201d says Kim.<\/p>\n
The exact origins of mitochondria are murky, but the leading theory holds that the organelle\u2019s story started around 1.5 billion years ago when a single-celled microorganism called an archaeon gobbled up a roaming bacterium that survived inside its host. This event marked the beginning of the eukaryotes \u2014 the large group of organisms, including plants, animals and fungi, in which cells contain organelles that are enclosed inside membranes. The swallowed bacterium retained its characteristic circular DNA as it settled into its new home, but over time it sacrificed most of its genes to the nuclear genome of its host.<\/p>\n
In the evolutionary lineage that gave rise to humans and other animals, this genetic transfer whittled the resident bacterium\u2019s genome down to just 37 genes that code for 13 proteins involved in energy production, turning it into a specialized organelle.<\/p>\n
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The small amount of mitochondrial DNA that stuck around in animals differs in key ways from nuclear DNA, which in humans encodes around 20,000 genes. For a start, mtDNA is typically inherited solely from the mother. There can be several copies of mtDNA in each mitochondrion, and the organelle has its own built-in machinery for making RNA and proteins from that DNA.<\/p>\n
Mitochondrial DNA is also much more error-prone, with a mutation rate estimated to be 10\u201320 times greater than that of nuclear DNA. This is in part because it has to contend with a barrage of damaging reactive oxygen species \u2014 unstable molecules that are generated in mitochondria during normal energy production. But it\u2019s also because it doesn\u2019t have histones: the proteins that protect and package nuclear DNA.<\/p>\n
Compared with its counterpart in the nucleus, mtDNA\u2019s toolkit for repairing itself is rudimentary. The nucleus is quick to fix a snapped DNA strand using an arsenal of repair mechanisms, but mitochondria can mend only some defects. They often simply throw away their broken DNA. This difference limits the options for gene-editing tools, because nearly all such tools for nuclear DNA use its inherent repair pathways.<\/p>\n
It has been notoriously challenging to develop approaches for modifying mitochondrial DNA, says Stephen Ekker, a molecular biologist at the University of Texas at Austin. \u201cIts bacterial origins are revealed when you start trying to edit it,\u201d he says.<\/p>\n
The most crucial hurdle for scientists trying to tinker with the mitochondrial genome is that it is locked behind a wall of membranes that doesn\u2019t allow external nucleic acids to pass into the organelle. Although there have been hints that CRISPR-based gene-editing tools \u2014 which rely on RNA to guide them to the correct sequence \u2014 might be able to overcome these barriers, many researchers remain unconvinced.<\/p>\n
Still, there are other ways in. More than a decade before CRISPR became a research tool, mitochondria researchers began experimenting with other editing tools that could cross mitochondrial membranes and coax the organelles into ditching their problematic DNA2.<\/p>\n
Every cell contains a vast number of mitochondrial genomes, because cells contain thousands of mitochondria and each one can carry several copies of mtDNA. Healthy and mutated mtDNA often coexist: a state known as heteroplasmy. It\u2019s when the proportion of mutated mtDNA reaches 60\u201380% in a particular tissue or cell type that mitochondrial diseases manifest3.<\/p>\n
Cells are swapping their mitochondria. What does this mean for our health?<\/p>\n<\/p>\n
If researchers could reduce the faulty copies of mtDNA in cells, they could eliminate the resulting disease. So, they turned to enzymes called zinc finger nucleases (ZFNs) and transcription activator-like effector nucleases (TALENs) to snip the double-stranded mtDNA. Whereas targeted snipping of nuclear DNA cajoles the cut DNA strands to glue themselves back together without the harmful mutation, the cut DNA in mitochondria is simply cast out. This elimination triggers the remaining intact copies to replicate themselves so that the correct level of mtDNA is maintained.<\/p>\n
In most cases, the mutated copies will be reduced to an acceptable level as the normal copies are replicated. \u201cThat\u2019s going to make up for what you\u2019re destroying,\u201d says Carlos Moraes, a geneticist at the University of Miami in Florida.<\/p>\n
Although there has been progress with this approach, it hasn\u2019t made its way out of the laboratory. And even if it did reach the clinic, the technique would be powerless against diseases caused by mutations that are often present in all copies of a person\u2019s mtDNA, such as Leber\u2019s hereditary optic neuropathy (LHON), a rare condition that causes rapid vision loss.<\/p>\n
What researchers need are tools that do more than cut DNA but that don\u2019t rely on guide RNA.<\/p>\n
When CRISPR\u2013Cas9 emerged as a tool in 2012, it became the go-to gene editor for all kinds of application. A guide RNA directs the Cas9 enzyme to a specific DNA sequence, where the enzyme does the cutting. Genetic changes are introduced as the DNA repairs itself.<\/p>\n
The approach became even more useful in 2016, when David Liu, a chemical biologist at the Broad Institute of MIT and Harvard in Cambridge, Massachusetts, and his colleagues introduced a more precise technique called base editing4. In this case, researchers modify the Cas9 enzyme and rely on another enzyme, called a deaminase, to convert one DNA base letter to another \u2014 such as cytosine (C) to thymine (T) or adenine (A) to guanine (G).<\/p>\n
Hope, despair and CRISPR \u2014 the race to save one woman\u2019s life<\/p>\n<\/p>\n
Although base editing and other CRISPR techniques took off for nuclear DNA, Liu and other research teams couldn\u2019t get it working on mtDNA. Because CRISPR\u2019s guide RNA doesn\u2019t readily pass through a mitochondrion\u2019s double membrane, using precise tools on mtDNA remained a pipe dream. \u201cWe did not have much success,\u201d says Liu. <\/p>\n
A solution materialized in 2018 when Joseph Mougous, a microbiologist then at the University of Washington in Seattle, and his colleagues stumbled across a toxin made by the bacterium Burkholderia cenocepacia. This enzyme, a deadly weapon against other bacteria, wreaks havoc by ultimately converting base C to T across the bacterial genome5.<\/p>\n
Mougous, now based at Yale University in New Haven, Connecticut, e-mailed Liu asking whether the enzyme, called DddA, would be of any use to him. \u201cI knew exactly what it might be used for \u2014 base editing mtDNA!\u201d says Liu. <\/p>\n
But switching every C to a T would be lethal to cells. Liu and his colleagues set out to \u201ctame the beast\u201d. They split DddA into two inactive pieces so that the enzyme would do its handiwork on mtDNA only when the pieces were brought together in a particular orientation. And instead of using guide RNA, Liu and his colleagues modified proteins found in TALENs to direct the DddA segments to their target sequences (see \u2018Making the edit\u2019).<\/p>\n","protected":false},"excerpt":{"rendered":"
CRISPR gene editing has made its way into every corner of modern biology, but not into every corner of the cell. Although researchers have used these systems to develop treatments for sickle-cell anaemia and blood cancers, to unlock the secrets of multicellularity and to discover the role of thousands of overlooked proteins, there\u2019s one place<\/p>\n","protected":false},"author":1,"featured_media":28042,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[58],"tags":[6485,4097,2419],"class_list":{"0":"post-28041","1":"post","2":"type-post","3":"status-publish","4":"format-standard","5":"has-post-thumbnail","7":"category-science","8":"tag-easier","9":"tag-fixing","10":"tag-lot"},"_links":{"self":[{"href":"https:\/\/naijaglobalnews.org\/index.php?rest_route=\/wp\/v2\/posts\/28041","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/naijaglobalnews.org\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/naijaglobalnews.org\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/naijaglobalnews.org\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/naijaglobalnews.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=28041"}],"version-history":[{"count":0,"href":"https:\/\/naijaglobalnews.org\/index.php?rest_route=\/wp\/v2\/posts\/28041\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/naijaglobalnews.org\/index.php?rest_route=\/wp\/v2\/media\/28042"}],"wp:attachment":[{"href":"https:\/\/naijaglobalnews.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=28041"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/naijaglobalnews.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=28041"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/naijaglobalnews.org\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=28041"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}