Chromosome Y News and Research

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The Y chromosome is one of the two sex chromosomes in humans (the other is the X chromosome). The sex chromosomes form one of the 23 pairs of human chromosomes in each cell. The Y chromosome spans about 58 million base pairs (the building blocks of DNA) and represents almost 2 percent of the total DNA in cells.

Each person normally has one pair of sex chromosomes in each cell. The Y chromosome is present in males, who have one X and one Y chromosome, while females have two X chromosomes.

Identifying genes on each chromosome is an active area of genetic research. Because researchers use different approaches to predict the number of genes on each chromosome, the estimated number of genes varies. The Y chromosome likely contains between 70 and 200 genes. Because only males have the Y chromosome, the genes on this chromosome tend to be involved in male sex determination and development. Sex is determined by the SRY gene, which is responsible for the development of a fetus into a male. Other genes on the Y chromosome are important for male fertility.

Many genes are unique to the X or Y chromosome, but genes in an area known as the pseudoautosomal region are present on both chromosomes. As a result, men and women each have two functional copies of these genes. Many genes in the pseudoautosomal region are essential for normal development.

Genes on the Y chromosome are among the estimated 20,000 to 25,000 total genes in the human genome.
New insight on jumping genes

New insight on jumping genes

Gene may hold key to future cancer hope

Gene may hold key to future cancer hope

Three new genes found that cause lung cancer

Three new genes found that cause lung cancer

Researchers restore memory process in fragile X syndrome

Researchers restore memory process in fragile X syndrome

Genes that increase rheumatoid arthritis risk found

Genes that increase rheumatoid arthritis risk found

Ground-breaking techniques to study telomeres in human cells may lead to early cancer detection

Ground-breaking techniques to study telomeres in human cells may lead to early cancer detection

Fetal cell transplant could be a hidden link between childbirth and reduced risk of breast cancer

Fetal cell transplant could be a hidden link between childbirth and reduced risk of breast cancer

Fetal cell "transplant" could be a hidden link between childbirth and reduced risk of breast cancer

Fetal cell "transplant" could be a hidden link between childbirth and reduced risk of breast cancer

Discovery of new pathway causing cell death related to frontotemporal dementia and ALS

Discovery of new pathway causing cell death related to frontotemporal dementia and ALS

Rapid testing for pre-natal detection of Down syndrome

Rapid testing for pre-natal detection of Down syndrome

Rheumatoid arthritis genes

Rheumatoid arthritis genes

Gene profiling can single out the worst cases of multiple myeloma and guide therapy

Gene profiling can single out the worst cases of multiple myeloma and guide therapy

Chronic stress can steal years from caregivers' lifetimes

Chronic stress can steal years from caregivers' lifetimes

New understanding of gene mutation responsible for fragile X syndrome

New understanding of gene mutation responsible for fragile X syndrome

New insight into the mechanisms of Lou Gehrig's disease

New insight into the mechanisms of Lou Gehrig's disease

Unique role for blood formation gene MLL identified

Unique role for blood formation gene MLL identified

Ultraconserved non-coding RNAs may be important in human cancer

Ultraconserved non-coding RNAs may be important in human cancer

New genetic risk factor for rheumatoid arthritis and lupus

New genetic risk factor for rheumatoid arthritis and lupus

Congestive heart failure is rare among leukemia patients who take imatinib

Congestive heart failure is rare among leukemia patients who take imatinib

First individual genome sequence of one person

First individual genome sequence of one person

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