Study finds protein is required for human chromosome productionOctober 13, 2005CHAPEL HILL - Scientists at the University of North Carolina at Chapel Hill School of Medicine have identified an elusive protein that performs a necessary step in the production of human chromosomes. The new study appears in the most recent issue (Oct. 7) of the journal Cell. The study found that a protein called CPSF73 acts like scissors to cut strands of histone messenger RNA (mRNA) in the cell nucleus. This cutting action produces the mRNA needed to create histone proteins that combine with DNA to form chromosomes. Like all other proteins, histones are made when a specialized RNA molecule is "read" by ribosomes, the cell's protein factories. The type of RNA, which relays information from the DNA (inside the nucleus) to the ribosome (outside the nucleus), is called messenger RNA. RNA that is not cut by CPSF73 is destroyed in the nucleus and never becomes messenger RNA, said Dr. William Marzluff, senior author of the study and Kenan distinguished professor of biochemistry and biophysics in UNC's School of Medicine. "This cutting of histone messenger RNA takes place as growing cells prepare to divide and is absolutely necessary for their eventual division," Marzluff said. Histone proteins help organize and compact within the nucleus the 6 billion nucleotides, or DNA bases, that make up the human genome - combinations of "A's," "T's," "G's" and "C's." Without histones, cells cannot survive. Dr. Zbigniew Dominski, associate professor of biochemistry and biophysics, has been searching for the protein that cuts histone messenger RNA since joining forces with Marzluff 10 years ago. He is the corresponding and lead author of the study. When RNA is first made from DNA, it is premature and cannot direct the synthesis of its corresponding protein until it is processed into mature messenger RNA, which includes being cut at a specific site, Dominski said. "This is a very complex process that requires many proteins to bind to the RNA molecule and show the cutting enzyme where to cleave the RNA," he added. Dominski was able to duplicate, in a test tube, the histone mRNA processing that takes place normally inside a cell's nucleus. However, the RNA cutting reaction was so quick that he was unable to determine which of the countless proteins inside the test tube was responsible. "We set a trap by subtly changing the chemical makeup of the histone messenger RNA right where it is cut. This allows the protein to still come to the RNA but forces it to cut more slowly," Dominski said. By slowing down the reaction, Dominski had enough time to irreversibly attach the RNA cutting protein, or nuclease, to the RNA itself using ultraviolet light as a cross-linking agent. Once attached to the RNA, the long-sought-after nuclease was trapped, allowing its subsequent identification. The discovery that the RNA cutting protein is CPSF73 was unexpected. This protein was already connected with processing of a completely different class of messenger RNA, polyadenylated mRNAs. These messenger RNAs serve as blueprints for all proteins other than the histones. "In terms of evolution, all messenger RNAs appear to be made with the aid of the same protein, CPSF73," Marzluff said. "This suggests that the two mRNA processing mechanisms, for polyadenylated and histone mRNAs, are distantly related." The authors further demonstrate that CPSF73 not only cuts the histone messenger RNA molecule in two, but also then chews the unneeded portion of the histone mRNA molecule into pieces. It is rare to find two such activities within a single protein, Dominski said. "From the point of view of understanding biology, our findings provide a unified mechanism for the synthesis of all messenger RNAs," Marzluff said. UNC School of Medicine technician and co-author Xiao-cui Yang assisted Dominski and Marzluff in this study. Their work was supported by a grant from the National Institutes of Health. University of North Carolina School of Medicine |
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| Related Human Chromosome Current Events and Human Chromosome News Articles CSHL-led team discovers rare mutation dramatically increasing schizophrenia risk An international team of researchers led by geneticist Jonathan Sebat, Ph.D., of Cold Spring Harbor Laboratory (CSHL), has identified a mutation on human chromosome 16 that substantially increases risk for schizophrenia. Scientists demonstrate link between genetic defect and brain changes in schizophrenia Researchers at the University of North Carolina at Chapel Hill School of Medicine have found that the 22q11 gene deletion - a mutation that confers the highest known genetic risk for schizophrenia - is associated with changes in the development of the brain that ultimately affect how its circuit elements are assembled. Dogs, Humans, put Heads Together to Find Cure for Brain Cancer Pinpointing the genes involved in human brain cancer can be like looking for a needle in a haystack, and sometimes the needle you find may not be the right one. Perfect pitch study offers window into influences of nature and nurture Practice, practice, practice might get you to Carnegie Hall, but for aspiring musicians, there's new evidence that genes may influence one's ability to get there, as well. DNA variations linked to brain tumors Mayo Clinic researchers and colleagues at the University of California San Francisco (UCSF) have found a connection between DNA alterations on human chromosome 9 and aggressive brain cancer known as glioblastoma. Role for CISD2 gene in human disease and lifespan control In the May 15th issue of G&D, Dr. Ting-Fen Tsai (The National Yang-Ming University, Taiwan) and colleagues present a new animal model of human Wolfram Syndrome, and effectively link CISD2 gene function, mitochondrial integrity and aging in mammals. New insights into progressive hearing loss In parallel studies in human and mouse, two groups of researchers have come to the same conclusion: that a new kind of gene is associated with progressive hearing loss. Team finds breast cancer gene linked to disease spread A team of researchers at Princeton University and The Cancer Institute of New Jersey has identified a long-sought gene that is fatefully switched on in 30 to 40 percent of all breast cancer patients, spreading the disease, resisting traditional chemotherapies and eventually leading to death. Newly-discovered mechanism can explain the Beckwith-Wiedemann syndrome Researchers from Uppsala University have discovered a mechanism that silences several genes in a chromosome domain. The findings, published in today's on-line issue of Molecular Cell, have implications in understanding the human disorder Beckwith-Wiedemann syndrome. Aberrations in region of chromosome 1q21.1 associated with broad range of disorders in children Researchers have discovered a submicroscopic aberration in a particular region of human chromosome 1q21.1 that appears to be associated with a variety of developmental disorders in children. More Human Chromosome Current Events and Human Chromosome News Articles |
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