What is the News ?

Scientists have fully sequenced the Y chromosome for the first time, uncovering information that could have implications for the study of male infertility and other health problems.

Facts About:

• In the nucleus of a human cell, each DNA molecule is packaged into a long thread like structure called chromosome. 
• Most human cells contains 23 pairs of chromosomes. One half of each pair of chromosomes from one parent, while other half comes from other parent.
• The 23rd pair are X and Y chromosomes, often called as sex chromosomes.  The other 22 pairs called as autosomes.
• Females have a pair of X chromosomes, whereas males have X and Y chromosome.
• The Y chromosome is male-determining because it bears a gene called SRY, which directs the development of a ridge of cells into a testis in the embryo. 
• The embryonic testes make male hormones, and these hormones direct the development of male features in a baby boy.

What is the difficulty in sequencing Y chromosome?

• Repetition - The Y chromosome was a particularly hard nut to crack because it is unusually repetitive.
• While all human chromosomes contain repeats, more than 30 million letters of the Y chromosome — out of 62.5 million — are repetitive sequences, sometimes called satellite DNA or junk DNA.
• Repetitive DNA complicates the assembling of data from genetic sequencing.
• Palindromes - The Y chromosome also contains palindromes — sequences of letters that are the same backward and forward, like radar. 
• Degeneration of Proto- Y - The proto-Y is degenerating at a faster pace, losing about 10 active genes per million years, reducing the number from its original 1,000 to just 27.
• There has been great debate about whether this degradation continues, because at this rate the whole human Y would disappear in a few million years

How the scientists unravelled the complex Y chromosome?

• Sequencing - Advanced "long-read" sequencing technology and computational methods enabled researchers to achieve a complete reading of the Y chromosome.
• This accomplishment added over 30 million repetitive base pairs to the human reference genome.
• The new technology has allowed sequencing of bases along individual long DNA molecules, producing long-reads of thousands of bases. 
• It effectively dealt with repetitive sequences and transformed raw sequencing data into a usable resource. 
• These longer reads are easier to distinguish and can therefore be assembled more easily.
• Findings- Overall, the combined research determined that the Y chromosome has 106 protein-coding genes. 
• 42 were found that were new, but many still appear to be repeats.

What is the importance of the study?

• Advanced diagnostics- The study empowers future sequencing endeavours to explore into health and disease aspects through comprehensive Y chromosome inclusion.
• To study whether loss of the Y chromosome is a biomarker of biological aging or has a direct effect on the health of men.
• Infertility- It will help to study conditions and disorders linked to the chromosome, such as lack of sperm production that leads to infertility.
• Health- Genes have been identified on the Y chromosomes that have been shown to be required for the prevention of cancer and cardiovascular disease.
• Dark matter- It represents the ‘dark matter’ of the genome. This analysis will allow us to better understand the regions of the Y chromosome that have regulatory functions and may encode mRNA and proteins.
• Human evolution- Assembling complete sequences of Y chromosomes across space and time not only helps to investigate sex chromosome evolution but also human evolution.
• Gene therapy- It will open up avenues to treat diseases that may linked to Y chromosomes.
• Future studies- The findings provide a solid base to explore how genes for sex and sperm work, how the Y chromosome evolved, and whether as predicted will disappear in a few million years.

Source: https://www.thehindu.com/sci-tech/science/y-male-chromosome-gene-sequencing-sry-gene-sequencing-evolution/article67230274.ece