Saturday, November 16, 2024
The Genetic 'Switch" Behind Parrot Color Diversity
Tuesday, November 12, 2024
Bird Beaks and Parrot Pigmentation
Authors Simon Griffith and Daniel Hooper make two very straightforward, yet interesting findings in their article "A single atom can change the colour of a bird. These are the genes responsible," published in the The Conversation. The findings are based off of two different research papers on pigmentation in birds, focusing on the biochemical reasons for different colors in Pseudeos fuscata, otherwise known as the Dusky Lory.
It turns out that two different genes are responsible for the red-to-yellow color range found these birds. These genes control a single enzyme, which converts red pigments to yellow. In the dusky lory, mutations in the genes cause the enzyme to become inactive, but only in certain parts of the bird. This is why some dusky lories have yellow beaks but red bodies; the genes in the beak cells are mutated, but not in the body cells.
Parrots are really unique in that their pigmentation come from psittacofulvins, a special pigment made by and found in parrots. Most other birds' pigmentation come from their food. I think that this makes parrots much more interesting to study, since their genetic basis for color can lead to much more variation among individuals. Perhaps different kinds of mutations in the dusky lory's genes can lead to more colors besides yellow and red. Albino individuals may also exist.
Monday, November 20, 2023
Loss of pigmentation in the skin due to the genetics: Vitiligo
Vitiligo is a genetic condition that creates a loss of pigmentation in patches. Hair on these regions may also lose pigment and appear as white. This condition can appear at any age, and the size of the patches varies between individuals. Most commonly these patches can appear on the face, ears, scalp, and limbs. Although considered an autoimmune disorder, genetics do have a role in this condition. The inheritance pattern for this condition is more complex, as it can be passed down from parents to offspring, but that is not a guarantee as vitiligo can happen at any age at random.
This condition is extremely fascinating as it has no effect on the individual other than loss of pigmentation. Studying this condition and find out if there’s a way to prevent this condition lies within the genome potentially.
Link to article: https://medlineplus.gov/genetics/condition/vitiligo/#inheritance
Sunday, November 12, 2017
Genes for Skin Color Variation

Saturday, September 23, 2017
Optix gene responsible for butterfly wing color
I personally find this study to be very fascinating. It makes me wonder if we would be able to do this with humans in the near future. However, I wonder if we would be able do this, would it be a cause for humans to have albinism, since the gene responsible for the melanin production in our eyes to become non-existent. I think it might become most likely become a very prominent phenotype if this would become successful, since the gene would have been removed entirely from original person. Overall, I find this study to be very interesting, and I wonder if similar procedures and experiments will be done in order to alter the appearance of humans and other animals.
Monday, November 21, 2016
CCMB Scientists Unravel Skin Colour Genetics of Indians
Accordingly, Brahmins of Uttar Pradesh have the fairest skin while Manjhis (Majhwars) have the darkest skin (highest skin pigmentation). Bhagats exhibit maximum variation in skin pigmentation. Four social groups — general, scheduled caste, other backward caste and religious group — were studied. The results were published in The Journal of Investigative Dermatology.
The association of rs1426654, a key single nucleotide polymorphism (SNP) in SLC24A5 gene, with skin colour has been well established. In fact, this SNP explains 25-38 per cent of pigmentation differences between Europeans and west Africans. “In addition to rs1426654, our study found another SNP (rs2470102) to be significantly associated with skin colour in the Indian population,” says Kumarasamy Thangaraj from the Centre for Cellular and Molecular Biology (CCMB), Hyderabad and the corresponding author of the paper.
The new SNP was found to independently affect skin pigmentation variation among the Indian population. While the well known SNP (rs1426654) has been found to have a significantly larger effect on skin colour ranging from Europeans to western Africans, the new SNP that the Indian researchers discovered is predominant in India/Asia. But both SNPs taken together are able to better explain the variation in skin colour among the Indian population than each of the SNP individually. The two SNPs together account for over 38 per cent of the variability in skin colour in the Indian population. The researchers compared the skin colour with the genotype of the individuals. Homozygous (similar) mutant alleles tend to cause lighter skin colour while homozygous wild alleles tend to cause darker skin colour. “So those with homozygous mutant alleles of the new SNP had fairer skin compared with those who had homozygous wild type alleles,” he says. The difference in skin colour persisted even when the contribution by the well known SNP was adjusted. “This shows that the new SNP has an independent effect on skin colour,” says Dr. Thangaraj.
People who had a combination of similar (homozygous) mutant alleles of both the new and the known SNP had the fairest skin; they are said to belong to the H1 haplotype. The frequency of the H1 haplotype was far higher (96 per cent) in people with lighter skin than in darker skin (37 per cent). “A particular haplotype is not exclusive to a social category. Though the frequency is less, we do find H1 haplotype in dark skinned social category. This is why we have fair-skinned people even in the dark skin social category and dark-skinned people in the otherwise fair skin social category,” he says.
In a subsequent study, Dr. Thangaraj and his team genotyped 1,825 individuals belonging to 52 diverse populations in India. They found the allele frequencies of the two SNPs were similar among the Indian population and spread across the population. “Like in Uttar Pradesh and Bihar, the proportion of both mutant and wild homozygous alleles is distributed in differently frequencies in different populations across the Indian population. Also, the H1 haplotype was not exclusive to any particular population or social category,” he says.
The study found that ultraviolet radiation-based selection model alone cannot account for the entire range of variation in skin colour seen in the Indian population. Rather, it is interplay between selection pressure for lighter skin in response to relatively less sunlight and admixture of the two founding populations of India.