StemCell Therapy

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Rocks dont care if they break. The very concepts of proofreading and repair imply accuracy for a purpose. In cells, complex multi-part machines find errors and fix them. Is this not evidence of intentionality and programming? As these new research papers show, the machines involved show exquisite craftsmanship and efficient action to keep other parts machines outside their own structural needs humming along.

How can they do that? How do they know? They bear an uncanny resemblance to surgeons or linemen that are trained as first responders to potentially catastrophic situations, and yet they work robotically in the dark without eyes or brains. Such things do not just appear by blind material processes. Proofreading and repair systems had to be operational from the beginning of life, because considering the lethal consequences without them, its hard to conceive of any primitive organism surviving, let alone progressing up an evolutionary ladder. Now, behold in wonder what is going on in our cells.

Before cells divide, billions of DNA base pairs must be precisely duplicated. About one time in 10 million, a wrong base is inserted into the copy. Researchers at North Carolina State University found genome guardians that stop and reel in DNA during this important operation. Two enzymes cooperate to proofread the copy. They halt the duplication when a mismatch is found until more machines can fix the error.

A pair of proteins known as MutS and MutL work together to initiate repair of these mismatches. MutS slides along the newly created side of the DNA strand after its replicated, proofreading it. When it finds a mismatch, it locks into place at the site of the error and recruits MutL to come and join it. MutL marks the newly formed DNA strand as defective and signals a different protein to gobble up the portion of the DNA containing the error. Then the nucleotide matching starts over, filling the gap again. The entire process reduces replication errors around a thousand-fold, serving as one of our bodys best defenses against genetic mutations that can lead to cancer. [Emphasis added.]

Well, is that not a tragedy for Darwin? Evolutionists need those mutations to build eyes and wings!

When cells divide, double-stranded breaks can occur. These are particularly dangerous, often associated with cancer. Medical researchers at University of Texas Health in San Antonio confirm that DNA repair requires multiple tools. Drs. Daley, Sung, and Burma at UT knew that the repair operation, called homologous recombination, is done by resection enzymes, but they were curious why so many different enzymes were involved. Why does the cell need three or four different enzymes that seem to accomplish the same task in repairing double-strand breaks? The perceived redundancy, they concluded, is really a very nave notion. Like a skilled workman, the cell maintains An array of tools, each one finely tuned.

Its like an engine mechanic who has a set of tools at his disposal, Dr. Sung said. The tool he uses depends on the issue that needs to be repaired. In like fashion, each DNA repair tool in our cells is designed to repair a distinctive type of break in our DNA.

Another type of error can occur when a gene is being transcribed. If RNA polymerase (RNAP, the transcribing machine) hits a lesion caused by UV radiation or some other mutagen, the transcription can stall. Thankfully, there is a programmed response called transcription-coupled nucleotide excision repair (TC-NER) that knows what to do. Thats a good thing, because faulty repair can lead to the severe neurological disorder Cockayne syndrome, characterized by microcephaly, delayed development, short stature, low weight gain, and numerous other problems like oversensitivity to sunlight, hearing loss, vision loss, severe tooth decay, bone abnormalities, hands and feet that are cold all the time, and changes in the brain that can be seen on brain scans (Genetics Home Reference).

Four researchers from Washington University, publishing in PNAS1, learned more about the poorly understood process of TC-NER, and revealed a plethora of molecular machines and factors involved. The initiation of TC-NER upon RNAP stalling requires specific factors, they begin. These factors respond rapidly to transcription-blocking DNA damage, binding to stalled RNAP to coordinate assembly of downstream NER factors. Moreover, the repair program must be able to handle a variety of situations. The technical details are too inscrutable for most readers to describe here (and this was about research on yeast!); suffice it to say that TC-NER is a well-choreographed, irreducibly complex process that, fortunately, works most of the time. Children with Type 2 Cockayne Syndrome may only live up to age 7 (NIH).

The cell has mechanisms for preventing errors, too. Research at Mt. Sinai Medical Center in New York City has unraveled for the first time the three-dimensional structure and mechanism of a complex enzyme that protects cells from constant DNA damage, opening the door to discovery of new therapeutics for the treatment of chemotherapy-resistant cancers. They used cryo-electron microscopy to study DNA polymerase at a near-atomic level. This important enzymes architecture and mechanism have been a mystery to scientists for years. Could any primitive life-form get by without something like this?

DNA polymerase is the crucial enzyme that allows cells to battle the more than 100,000 DNA-damaging events that occur daily from normal metabolic activities and environmental intrusions like ultraviolet light, ionizing radiation, and industrial carcinogens. The Mount Sinai team, which included first author Radhika Malik, PhD, Assistant Professor of Pharmacological Sciences, learned how the enzyme protects the cells from natural and manmade environmental as well cellular stresses through an intricate structure of four different proteins that connect to each other in a pentameric, or daisy chain-like, configuration.

Didnt the Darwinians tell us that UV light and ionizing radiation were sources of the building blocks of life and the mutations that nature can select to build humans from bacteria? No way. These findings are published in Nature Structural & Molecular Biology2.

DNA bases on opposite strands connect via hydrogen bonds, but sometimes a protein interloper makes a bogus connection. Covalent cross-links between proteins and DNA are among the most hazardous types of DNA damage, says the Ludwig-Maximilian University of Munich. Fortunately (again), theres an app for that.

Chemical lesions in the genetic material DNA can have catastrophic consequences for cells, and even for the organism concerned. This explains why the efficient identification and rapid repair of DNA damage is vital for survival. DNA-protein crosslinks (DPCs), which are formed when proteins are adventitiously attached to DNA, are particularly harmful. DPCs are removed by the action of a dedicated enzyme the protease SPRTN which cleaves the bond between the protein and the DNA.

DPCs can occur during natural metabolism or by contact with synthetic chemicals. SPRTN has a challenging job, they say, because it must be able to tackle a variety of situations; the enzyme has to be able to identify many different structures as aberrant. Its two domains must engage for it to recognize the error and fix it. Julian Stingele explains this fail-safe system:

One binds to double-stranded, and the other to single-stranded DNA. So the protein uses a modular system for substrate recognition. Only when both domains are engaged is the enzyme active and DNA in which double-stranded and single-stranded regions occur in close proximity is often found in the vicinity of crosslinks, says Stingele.

When this system isnt working properly, patients are subject to liver cancer and early aging.

We have just looked at five different types of errors that are repaired by five different systems of molecular machines. Each system must first recognize the error and then know what to do; otherwise, the consequences can be catastrophic. In each case, the machinery is well designed and finely tuned to solve the problem, and it does so rapidly and efficiently. That takes foresight, and foresight implies intelligent design. As Marcos Eberlin says in his book Foresight: How the Chemistry of Life Reveals Planning and Purpose, This act of anticipation foresight is not a characteristic of blind material processes. It is an act of intelligence, of a mind (p. 81).

See the original post:
In Cells, Proofreading and Repair Testify to Intelligent Design and Foresight - Discovery Institute

This entry was posted on September 11, 2020 at 3:51 pm and is filed under Molecular Genetics. You can follow any responses to this entry through the RSS 2.0 feed. Both comments and pings are currently closed. |