By Kenny Berkowitz –
As an undergraduate at Latvia’s Riga Technical University, Eriks Rozners found himself drawn to RNA, challenged by the complexity of its molecular structure, which is more flexible and less stable than that of DNA. Nearly 30 years later, the Binghamton University scientist has become a leader in the field, with a pair of recent grants from the National Institutes of Health and the National Science Foundation to keep doing what he does best: fundamental research into the chemistry and biochemistry of nucleic acids.
RNA (ribonucleic acid) is one of three major molecules essential for all known forms of life, along with DNA (deoxyribonucleic acid) and proteins.
“For a long time, people believed that RNA was simply a middleman, a worker that enabled the flow of genetic information from DNA to proteins,” says Rozners, an associate professor of chemistry. “Now, with the sequencing of the human genome, we know that only 2 percent of DNA encodes for proteins, while 70 to 90 percent is used to make RNA. That’s a lot of RNA, and even if we don’t yet understand it completely, we’re coming to appreciate that RNA is involved in the decision-making process of how cells develop.”
RNA, he notes, is an active player in cell development that determines which cells become skin, which become muscle, which become bone. “My lab is designing tools for the molecular recognition of different kinds of RNA, which can look very similar in cells, but are still significantly different,” Rozners says. “Such tools will enable studies on the various RNAs in their native environment, live cells.”
In the first project, “Amide-Modified RNA: Synthesis, Structure and Potential for RNA Interference,” Rozners and his collaborators — Martin Egli of Vanderbilt University, Kaizhang He of Dharmacon and Scott Kennedy of the University of Rochester — received a $1.5 million, four-year renewal grant from the National Institute of General Medical Sciences (NIGMS) to continue investigating the possibility of an artificial biopolymer that can mimic the properties of RNA.
In the second three-year project, “Sequence Selective Recognition of Double-Stranded Non-Coding RNA via Triplex Forming PNA,” the National Science Foundation awarded Rozners $414,767 to develop synthetic compounds that can differentiate between types of RNA by reading their sequence-specific nucleic codes. These compounds will be tested in collaboration with Paul Agris of the University at Albany, another SUNY institution.
Both projects are still years away from finding hands-on applications. But their potential, either as new research tools or as new medicines to target diseases that involve aberrant RNA expression, is enormous.
“This is difficult work, and Eriks is one of the few people who can do it, because it tends to be very elaborate, very complicated and very expensive” says Egli, an expert on X-ray crystallography. “Eriks is very meticulous, and has gone much further than previous attempts to study amides. He’s taking a much more holistic approach, focusing on the basic science of chemically modified nucleic acids and looking at fundamental changes all the way down to the atomic level.”
Source – SUNY Binghamton
By Kenny Berkowitz –
RNA (ribonucleic acid) is one of three major molecules essential for all known forms of life, along with DNA (deoxyribonucleic acid) and proteins.
RNA, he notes, is an active player in cell development that determines which cells become skin, which become muscle, which become bone. “My lab is designing tools for the molecular recognition of different kinds of RNA, which can look very similar in cells, but are still significantly different,” Rozners says. “Such tools will enable studies on the various RNAs in their native environment, live cells.”
In the first project, “Amide-Modified RNA: Synthesis, Structure and Potential for RNA Interference,” Rozners and his collaborators — Martin Egli of Vanderbilt University, Kaizhang He of Dharmacon and Scott Kennedy of the University of Rochester — received a $1.5 million, four-year renewal grant from the National Institute of General Medical Sciences (NIGMS) to continue investigating the possibility of an artificial biopolymer that can mimic the properties of RNA.
In the second three-year project, “Sequence Selective Recognition of Double-Stranded Non-Coding RNA via Triplex Forming PNA,” the National Science Foundation awarded Rozners $414,767 to develop synthetic compounds that can differentiate between types of RNA by reading their sequence-specific nucleic codes. These compounds will be tested in collaboration with Paul Agris of the University at Albany, another SUNY institution.
Both projects are still years away from finding hands-on applications. But their potential, either as new research tools or as new medicines to target diseases that involve aberrant RNA expression, is enormous.
Source – SUNY Binghamton
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By Kenny Berkowitz –
RNA (ribonucleic acid) is one of three major molecules essential for all known forms of life, along with DNA (deoxyribonucleic acid) and proteins.
RNA, he notes, is an active player in cell development that determines which cells become skin, which become muscle, which become bone. “My lab is designing tools for the molecular recognition of different kinds of RNA, which can look very similar in cells, but are still significantly different,” Rozners says. “Such tools will enable studies on the various RNAs in their native environment, live cells.”
In the first project, “Amide-Modified RNA: Synthesis, Structure and Potential for RNA Interference,” Rozners and his collaborators — Martin Egli of Vanderbilt University, Kaizhang He of Dharmacon and Scott Kennedy of the University of Rochester — received a $1.5 million, four-year renewal grant from the National Institute of General Medical Sciences (NIGMS) to continue investigating the possibility of an artificial biopolymer that can mimic the properties of RNA.
In the second three-year project, “Sequence Selective Recognition of Double-Stranded Non-Coding RNA via Triplex Forming PNA,” the National Science Foundation awarded Rozners $414,767 to develop synthetic compounds that can differentiate between types of RNA by reading their sequence-specific nucleic codes. These compounds will be tested in collaboration with Paul Agris of the University at Albany, another SUNY institution.
Both projects are still years away from finding hands-on applications. But their potential, either as new research tools or as new medicines to target diseases that involve aberrant RNA expression, is enormous.
Source – SUNY Binghamton
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Worm’s radical transformation shows metamorphosis can change the functions of cells
RNA sequencing reveals functional chimeric mRNAs in mammalian immunity
Atlas of the brain’s striatum could guide researchers to new drug treatments
Immune cells offer insights on billion-dollar virus
A functionally integrated cross-tissue alternative splicing program during short-term calorie restriction
Dietary oxidized plant sterol shifts macrophage state to fuel aortic inflammation
Unlocking the past – new method helps gain insights into old tissue
Novel AI model trained on RNA-Seq data accurately detects key gene mutations and predicts biomarkers across 32 cancer types
Transcriptomic aging clock reveals age-related molecular patterns in opioid dependence
RNA sequencing helps predict stem cell transplant benefit in pediatric AML
Protein ‘switch’ determines whether liposarcoma cells will become aggressive
Precursor tRNAs sense temperature changes: heat stress-induced capped pre-tRNAs suppress protein synthesis
Ketamine increases neuroplasticity in female mice but not in males
Somatic mutations linked to vascular damage in progeria
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Soluble signals released by neighboring cells direct how the human kidney is built
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Learning the grammar of gene regulation
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