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Lawrence C. Brody, Ph.D. defines Cytosine

Cytosine

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Cytosine (C) is one of four chemical bases in DNA, the other three being adenine (A), guanine (G), and thymine (T). Within the DNA molecule, cytosine bases located on one strand form chemical bonds with guanine bases on the opposite strand. The sequence of four DNA bases encodes the cell's genetic instructions.

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Cytosine

Cytosine (C) is one of four chemical bases in DNA, the other three being adenine (A), guanine (G), and thymine (T). Within the DNA molecule, cytosine bases located on one strand form chemical bonds with guanine bases on the opposite strand. The sequence of four DNA bases encodes the cell's genetic instructions.

Narration Transcription

Cytosine is one of the four building blocks of DNA and RNA. So it's one of the four nucleotides that's present both in DNA, RNA, and each cytosine makes up part of the code. Cytosine has the unique property in that it binds in the double helix opposite a guanine, one of the other nucleotides. Cytosine has one other interesting property that none of the other nucleotides have, is that very often in the cell, cytosine can have an extra chemical attached to them, a methyl group. And this DNA methylation at cytosines is thought helps regulate genes try to help turn them on and off.


Doctor Profile

Lawrence C. Brody, Ph.D.

Lawrence C. Brody, Ph.D.

Occupation
Chief & Senior Investigator, Genome Technology Branch; Head, Molecular Pathogenesis Section

Biography
Dr. Brody investigates the genetics of breast cancer and neural tube defects. As chief of the NHGRI Genome Technology Branch's Molecular Pathogenesis section, he is interested in studying genetic mutations that lead to perturbations in normal metabolic pathways and cause disorders such as cancer and birth defects. His laboratory investigates mutations in two breast cancer-linked genes, breast cancer gene 1 (BRCA1) and breast cancer gene 2 (BRCA2). Dr. Brody's laboratory was among the first to report that women carrying BRCA1 or BRCA2 mutations have a higher risk of developing both breast and ovarian cancer than women without such mutations.

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