Telomerase is involved in adding DNA to the end of the lagging strand.
At the ends of linear chromosomes (telomeres), telomerase uses its built-in RNA template to extend the parent DNA template near the end of the lagging strand, providing room for an RNA primer so that lagging strand synthesis can be completed to the end of the chromosome
<h2>Down Syndrome</h2>
Explanation:
Down syndrome is a genetic disorder caused when abnormal cell division results in an extra full or partial copy of chromosome 21
- Down syndrome is a genetic disorder caused when abnormal cell division results in an extra full or partial copy of chromosome 21
- Down syndrome is usually caused by an error in cell division called nondisjunction which results in an embryo with three copies of chromosome 21 instead of the usual two
- Prior to or at conception, a pair of 21st chromosomes in either the sperm or the egg fails to separates
- With development in embryo the extra chromosome is replicated in every cell of the body;this type of Down syndrome which accounts for 95% of cases is called trisomy 21
- Maternal age is the only factor that has been linked to an increased chance of having a baby with Down syndrome resulting from nondisjunction;here environmental agents such as drugs, chemicals, and radiation act as mutagens which induce mutation in the fetus
Sunlight Water and good soil
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An autosome is any of the 23 chromosomes which is not an X or Y chromosome. A sex chromosome is effectively the same as an autosome, apart from depending upon whether you inherit a Y chromosome or not, a sex chromosome<span> will determine your gender. Hence the name.</span>
