Indian-origin researcher detects 135 new melanin genes responsible for pigmentation

A recent study conducted by Indian-origin researcher has identified unknown genes linked to pigmentation. These genes could serve as potential targets for the development of drugs that modify melanin, aiding in the treatment of conditions like vitiligo and other pigmentation-related disorders. The skin, hair, and eye color are identified by melanin, a pigment that absorbs light. Vivek Bajpai, the lead research author, emphasized that comprehending the factors governing melanin could help protect lighter-skinned people from melanoma, or skin cancer. By targeting these new melanin genes, we could also develop melanin-modifying drugs for vitiligo and other pigmentation diseases, he added. The researchers found 169 functionally diverse genes that impacted melanin production. Of those, 135 were not previously associated with pigmentation. The article recently published in the ‘Science’ journal features research by Bajpai, an assistant professor in the School of Sustainable Chemical, Biological and Materials Engineering at the University of Oklahoma, and collaborators from Stanford University. Melanin is produced within special structures called melanosomes, which are found inside melanin-producing pigment cells called melanocytes. Although all humans have the same number of melanocytes, the amount of melanin they produce differs and gives rise to the variation in human skin colour. To understand what actually causes different amounts of melanin to be produced, we used a technology called CRISPR-Cas9 to genetically engineer cells, Bajpai said. “Using CRISPR, we systematically removed more than 20,000 genes from hundreds of millions of melanocytes and observed the impact on melanin production. Bajpai developed a novel method to detect and quantify the melanin-producing activity of melanocytes. By passing light through the melanocytes, he could record if the light was either absorbed or scattered by the melanin inside. If there are a lot of melanin-producing melanosomes, the light will scatter much more than in cells with little melanin, Bajpai said. Using a process called side-scatter of flow cytometry, we were able to separate cells with more or less melanin. These separated cells were then analyzed to determine the identity of melanin-modifying genes. We identified both new and previously known genes that play important roles in regulating melanin production in humans. Historically, darker pigmentation has been needed to protect against ultraviolet radiation in areas closer to the equator and for people who spend hours in direct sunlight. As humans moved into areas with less direct sunlight or fewer hours of daylight overall, less melanin was needed. Over time, this resulted in melanosomes that produced less melanin, thus absorbing more sunlight. The technology developed and used by the research team could also be applied to identify genes that regulate melanin production in fungi and bacteria. Melanin production in fungi and bacteria enables them to be more pathogenic to humans or crops. Researchers could develop effective interventions against these microbes and their diseases by discovering and targeting such melanin-producing genes. Bajpai’s role in the study was completed during his professorship at the University of Oklahoma. However, a portion of this research took place during his postdoctoral research fellowship at Stanford University. With inputs from PTI