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NPM1

NPM1

Reviewed January 2014

What is the official name of the NPM1 gene?

The official name of this gene is “nucleophosmin (nucleolar phosphoprotein B23, numatrin).”

NPM1 is the gene's official symbol. The NPM1 gene is also known by other names, listed below.

Read more about gene names and symbols on the About page.

What is the normal function of the NPM1 gene?

The NPM1 gene provides instructions for making a protein called nucleophosmin, which is found in a small region inside the nucleus of the cell called the nucleolus. Nucleophosmin shuttles back and forth between the nucleus and the fluid surrounding it (the cytoplasm). It is thought to play a part in many cellular functions, including processes involved in protein formation, DNA replication, and the progression of the cell through the step-by-step process it takes to replicate itself (called the cell cycle). In the nucleolus, nucleophosmin attaches to another protein called ARF, keeping it in the proper location and protecting it from being broken down. The ARF protein is considered a tumor suppressor because it is involved in pathways that prevent cells from growing and dividing in an uncontrolled way.

How are changes in the NPM1 gene related to health conditions?

cytogenetically normal acute myeloid leukemia - associated with the NPM1 gene

Mutations in the NPM1 gene are involved in a form of blood cell cancer known as cytogenetically normal acute myeloid leukemia (CN-AML). While large chromosomal abnormalities can be involved in the development of acute myeloid leukemia, about half of cases do not have these abnormalities; these are classified as CN-AML. Approximately 64 percent of people with CN-AML have a mutation in the NPM1 gene.

The NPM1 gene mutations involved in CN-AML are called somatic mutations; they are found only in cells that become cancerous and are not inherited. These mutations occur in a region of the gene designated exon 12. They change the blueprint used to make the nucleophosmin protein, leading to production of a protein with an altered sequence of protein building blocks (amino acids). The alterations change the amino acid tryptophan at protein position 290 and often the tryptophan at position 288. These two tryptophans are important for localization of the protein in the nucleolus. The new sequence also provides a signal (called the nuclear export signal) for the protein to be moved out of the nucleus. As a result, the nucleophosmin protein is found in the cytoplasm rather than the nucleolus.

It is not clear how abnormal localization of the nucleophosmin protein leads to acute myeloid leukemia. Research suggests that it affects the function of the ARF protein. Because of its interaction with the altered nucleophosmin, the ARF protein is also found in the cytoplasm in cells with these genetic changes. In addition, the altered nucleophosmin protein is unable to protect ARF from being broken down. A reduction of the tumor suppressor function of the ARF protein is believed to lead to the uncontrolled production of abnormal white blood cells that occurs in acute myeloid leukemia. Other effects of NPM1 gene mutations may also be involved in the development of leukemia.

other cancers - associated with the NPM1 gene

A genetic rearrangement (translocation) involving the NPM1 gene is found in another blood cell cancer known as anaplastic large cell lymphoma (ALCL). In ALCL, white blood cells known as T cells grow and divide uncontrollably and often form tumors in the lymph nodes. The translocation involved in this cancer, known as t(2;5), fuses part of the NPM1 gene on chromosome 5 with part of another gene called ALK on chromosome 2. This rearrangement is a somatic mutation.

The protein produced from the fusion gene is called NPM-ALK. Like the normal activated ALK protein, NPM-ALK turns on signaling pathways that stimulate cell growth and division (proliferation) and maturation (differentiation). Unlike ALK, the NPM-ALK protein is active all the time, which causes uncontrolled cell proliferation and leads to ALCL.

Genetics Home Reference provides information about acute promyelocytic leukemia, which is also associated with changes in the NPM1 gene.

Where is the NPM1 gene located?

Cytogenetic Location: 5q35.1

Molecular Location on chromosome 5: base pairs 171,387,647 to 171,410,883

The NPM1 gene is located on the long (q) arm of chromosome 5 at position 35.1.

The NPM1 gene is located on the long (q) arm of chromosome 5 at position 35.1.

More precisely, the NPM1 gene is located from base pair 171,387,647 to base pair 171,410,883 on chromosome 5.

See How do geneticists indicate the location of a gene? in the Handbook.

Where can I find additional information about NPM1?

You and your healthcare professional may find the following resources about NPM1 helpful.

You may also be interested in these resources, which are designed for genetics professionals and researchers.

What other names do people use for the NPM1 gene or gene products?

  • B23
  • NPM
  • NPM_HUMAN
  • nucleolar protein NO38
  • nucleophosmin
  • nucleophosmin/nucleoplasmin family, member 1

Where can I find general information about genes?

The Handbook provides basic information about genetics in clear language.

These links provide additional genetics resources that may be useful.

What glossary definitions help with understanding NPM1?

References (7 links)

 

The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? in the Handbook.

 
Reviewed: January 2014
Published: October 20, 2014