The four bases found in DNA are adenine (A), thymine (T), cytosine (C), and guanine (G).
Each nucleotide has three parts: a sugar molecule (deoxyribose), a phosphate group, and one of four nitrogenous bases (adenine, thymine, cytosine, or guanine).
DNA is the genetic material that contains all the information needed to build an organism.
The two strands of DNA are antiparallel, meaning they run in opposite directions.
DNA is a double-stranded molecule that forms a helical structure.
Each base on one strand pairs with its complementary base on the opposite strand, forming hydrogenbonds between them.
Nucleic acids store genetic information by encoding it as sequences of nucleotides.
Protein synthesis involves two main stages: transcription and translation.
Ribonucleic acid (RNA) differs from deoxyribonucleic acid (DNA) by having ribose instead of deoxyribose as its sugar component and uracil instead of thymine as its base.
There are different types of RNA based on their function, including messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA).
The sequence of bases along a single strand determines the genetic code of an organism.
Cytosine always pairs with guanine through three hydrogen bonds.
The sequence of nucleotides in DNA determines the genetic information carried by an organism.
Transcription occurs inside the nucleus where RNA polymerase reads the sequence of bases on a strand of DNA and makes a complementary copy of mRNA.
Adenine is complementary to thymine because they have similar chemical properties.
Thymine is found only in DNA, while uracil is found only in RNA.
Adenine always pairs with thymine or uracil through two hydrogen bonds.
Genetic mutations can occur due to errors during replication or exposure to environmental factors such as radiation or chemicals.
In DNA replication, two strands are made from one originaldouble-stranded DNA molecule.
Each base pair in DNA consists of one purine (adenine or guanine) and one pyrimidine (thymine or cytosine).
Mutations can be beneficial, neutral, or detrimental to an individual's survival.
During DNA replication, the two strands separate and serve as templates for the synthesis of new strands.
The sequence of bases on the template strand determines which bases will be added to the new strand.
During DNA replication, the two strands separate and serve as templates for new complementary strands.
The process of DNA replication involves unwinding the helix, separating the strands, synthesizing new nucleotides, and joining them together.
Point mutation: A change in a single nucleotide base pair within a gene.
Errors in DNA replication can lead to genetic mutations that may have consequences on gene expression and protein function.
The process of DNA replication is semiconservative because each daughter strand receives one old and one newly synthesized strand.
centromere is the part of the chromosome that connects the sister chromatids
Helicase unwinds a DNA strand
DNA polymerase adds complementary bases to the growing chain
The bond between a sugar and a phosphate molecule is called a phosphodiester bond and is a strong covelent bond
A nucleotide consists of three components: a pentose (5-carbon) sugar, a nitrogenous base, and a phosphate group
chromatin is DNA strands wrapped around histones to form chromosomes (decondensed chromatid)
A chromatid is condensed chromatin that is coiled into a chromosome. Sister chromatids when joined create a chromosome
Histone protiens are what DNA strands wrap arround to from chromatin
A Karyotype is a set of chromosomes from an organism
each chromosome holds different genes and is made up of DNA molecules
Plasmids are small amounts of DNA in prokaryotic cells that float freely in the cytoplasm
telomere is a short piece of DNA at the end of a chromosome that protects the chromosome from damage