The nuclear envelope is a double membrane composed of an outer and an inner phospholipid bilayer. The thin space between the two layers connects with the lumen of the rough endoplasmic reticulum (RER), and the outer layer is an extension of the outer face of the RER.

The inner surface of the nuclear envelope has a protein lining called the nuclear lamina, which binds to chromatin and other contents of the nucleus. The entire envelope is perforated by numerous nuclear pores. These transport routes are fully permeable to small molecules up to the size of the smallest proteins, but they form a selective barrier against movement of larger molecules. Each pore is surrounded by an elaborate protein structure called the nuclear pore complex, which selects molecules for entrance into the nucleus. Entering the nucleus through the pores are the nucleotide building blocks of DNA and RNA, as well as adenosine triphosphate, which provides the energy for synthesizing genetic material. Histones and other large proteins must also pass through the pores. These molecules have special amino acid sequences on their surface that signal admittance by the nuclear pore complexes. The complexes also regulate the export from the nucleus of RNA and subunits of ribosomes.

DNA in prokaryotes is also organized in loops and is bound to small proteins resembling histones, but these structures are not enclosed by a nuclear membrane.

The structure of DNA

Several features are common to the genetic structure of most organisms. First is the double-stranded DNA. Each strand of this molecule is a series of nucleotides, and each nucleotide is composed of a sugar-phosphate compound attached to one of four nitrogen-containing bases. The sugar-phosphate compounds link together to form the backbone of the strand. Each of the bases strung along the backbone is chemically attracted to a corresponding base on the parallel strand of the DNA molecule. This base pairing joins the two strands of the molecule much as rungs join the two sides of a ladder, and the chemical bonding of the base pairs twists the doubled strands into a spiral, or helical, shape.

The four nucleotide bases are adenine, cytosine, guanine, and thymine. DNA is composed of millions of these bases strung in an apparently limitless variety of sequences. It is in the sequence of bases that the genetic information is contained, each sequence determining the sequence of amino acids to be connected into proteins. A nucleotide sequence sufficient to encode one protein is called a gene. Genes are interspersed along the DNA molecule with other sequences that do not encode proteins. Some of these so-called untranslated regions regulate the activity of the adjacent genes, for example, by marking the points at which enzymes begin and cease transcribing DNA into RNA (see below Genetic expression through RNA).

Rearrangement and modification of DNA

Rearrangements and modifications of the nucleotide sequences in DNA are exceptions to the rules of genetic expression and sometimes cause significant changes in the structure and function of cells. Different cells of the body owe their specialized structures and functions to different genes. This does not mean that the set of genetic information varies among the cells of the body. Indeed, for each cell the entire DNA content of the chromosomes is usually duplicated exactly from generation to generation, and, in general, the genetic content and arrangement is strikingly similar among different cell types of the same organism. As a result, the differentiation of cells can occur without the loss or irreversible inactivation of unnecessary genes, an observation that is reinforced by the presence of specific genes in a range of adult tissues. For example, normal copies of the genes encoding hemoglobin are present in the same numbers in red blood cells, which make hemoglobin, as in a range of other types of cells, which do not.

Despite the general uniformity of genetic content in all the cells of an organism, studies have shown a few clear examples in some organisms of programmed, reversible change in the DNA of developing tissues. One of the most dramatic rearrangements of DNA occurs in the immune systems of mammals. The body’s defense against invasion by foreign organisms involves the synthesis of a vast range of antibodies by lymphocytes (a type of white blood cell). Antibodies are proteins that bind to specific invading molecules or organisms and either inactivate them or signal their destruction. The binding sites on each antibody molecule are formed by one light and one heavy amino acid chain, which are encoded by different segments of the DNA in the lymphocyte nucleus. These DNA segments undergo considerable rearrangements, resulting in the synthesis of a great variety of antibodies. Some invasive organisms, such as trypanosome parasites, which cause sleeping sickness, go to great lengths to rearrange their own DNA to evade the versatility of their hosts’ antibody production. The parasites are covered by a thick coat of glycoprotein (a protein with sugars attached). Given time, host organisms can overcome infection by producing antibodies to the parasites’ glycoprotein coat, but this reaction is anticipated and evaded by the selective rearrangement of the trypanosomes’ DNA encoding the glycoprotein, thus constantly changing the surface presented to the hosts’ immune system.

Careful comparisons of gene structure have also revealed epigenetic modifications, heritable changes that occur on the sugar-phosphate side of bases in the DNA and thus do not cause rearrangements in the DNA sequence itself. An example of an epigenetic modification involves the addition of a methyl group to cytosine bases. This appears to cause the inactivation of genes that do not need to be expressed in a particular type of cell. An important feature of the methylation of cytosine lies in its ability to be copied, so that methyl groups in a dividing cell’s DNA will result in methyl groups in the same positions in the DNA of both daughter cells.