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BizportalHealth

Weizmann Institute Study Reveals Proteins Differ From DNA Blueprints

Translated & summarized from Bizportal by baba

BusinessNeutral tone

Hebrew · 1 newsroom

A Weizmann Institute study published in Nature reveals that thousands of protein variations in humans do not stem from DNA sequences. These non-genetic protein changes, observed across healthy tissues, suggest environmental factors and cellular processes influence protein function beyond genetic code, impacting disease understanding and personalized medicine.

The story in 5 lines · by baba

  • Thousands of protein variations in humans are not explained by DNA sequences.
  • Weizmann Institute research found these non-genetic protein changes in healthy tissues.
  • Cellular environment and translation errors may cause these protein alterations.
  • Findings suggest a new layer of biological regulation beyond genetics.
  • Implications for understanding human diversity and personalized medicine are significant.

A new study from the Weizmann Institute of Science, published in the journal Nature, has found that thousands of protein variations in the human body do not originate from the DNA sequence itself. While DNA is traditionally viewed as the body's instruction manual, dictating traits like eye color and predisposition to diseases, this research indicates a more complex reality. Proteins, the workhorses of genetic instructions, can undergo modifications during their creation that result in a product slightly different from what the DNA initially coded for.

Researchers, led by Professor Itzhak Pilpel, analyzed genetic and protein data from 29 healthy human tissues. They identified 13,910 instances where a single amino acid in a protein was replaced by another, representing 7,215 unique substitution types. In some cases, these changes were traceable to genetic variations or mutations in the DNA. However, in a significant number of instances, the observed protein alteration could not be explained by the individual's genetic sequence, suggesting a layer of biological regulation beyond the DNA itself.

The study found that these non-genetic protein variations are not always random occurrences. Hundreds of these altered protein versions appeared consistently across multiple healthy individuals and were located in functionally important regions of the proteins. The researchers also experimentally validated some of these non-genetic changes. This suggests that these variations may represent a broader biological mechanism rather than isolated errors.

One potential source of these discrepancies lies in the translation process, where the cell converts DNA information into proteins. Errors can occur during this process, leading to the incorporation of different amino acids than those specified by the genetic code. Furthermore, the study observed a correlation between cellular environmental conditions, such as amino acid deprivation, and specific patterns of non-genetic protein changes. This implies that the cellular environment can influence how genetic instructions are ultimately translated into functional proteins.

These findings have significant implications for understanding human diversity and disease. They suggest that even individuals with identical DNA sequences may produce slightly different sets of proteins, contributing to variations in traits and health outcomes. While genetics remains a primary determinant, this research adds a crucial layer of understanding by highlighting how post-DNA processes and environmental factors can shape the proteome. The study opens new avenues for personalized medicine, potentially improving disease diagnosis and treatment by considering protein variations that are not directly encoded in the DNA.

BizportalOther · Tel Aviv

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