Hoppa till huvudinnehåll

DNA methyltransferase 1

Den DNMT1 gene provides instructions for making an enzyme called DNA methyltransferase 1. This enzyme is involved in DNA methylation, which is the addition of methyl groups, consisting of one carbon atom and three hydrogen atoms, to DNA molecules. In particular, the enzyme helps add methyl groups to DNA building blocks (nucleotides) called cytosines.

Normal function

Den DNMT1 gene provides instructions for making an enzyme called DNA methyltransferase 1. This enzyme is involved in DNA methylation, which is the addition of methyl groups, consisting of one carbon atom and three hydrogen atoms, to DNA molecules. In particular, the enzyme helps add methyl groups to DNA building blocks (nucleotides) called cytosines.

DNA methylation is important in many cellular functions. These include determining whether the instructions in a particular segment of DNA are carried out or suppressed (gene silencing), regulating reactions involving proteins and fats (lipids), and controlling the processing of chemicals that relay signals in the nervous system (neurotransmitters). DNA methyltransferase 1 is active in the adult nervous system. Although its specific function is not well understood, the enzyme may help regulate nerve cell (neuron) maturation and specialization (differentiation), the ability of neurons to move (migrate) and connect with each other, and neuron survival.

Conditions referring to this gene or chromosome

Other names

AIM

CXXC finger protein 9

CXXC-type zinc finger protein 9

CXXC9

DNA (cytosine-5)-methyltransferase 1

DNA (cytosine-5-)-methyltransferase 1

DNA methyltransferase HsaI

DNA MTase HsaI

DNMT

DNMT1_HUMAN

HSN1E

m.HsaI

MCMT

Related patient information and medicines

Narkolepsi och kataplexi

Patient information leaflet

Narkolepsi och kataplexi

The exact cause of this is uncertain. It has been suggested that narcolepsy with cataplexy is a type of autoimmune disease. In autoimmune disease the body makes antibodies which damage normal cells in the body. If you are taking 'the pill' you should discuss this with your doctor. Methylphenidate och amphetamines Older stimulant medicines used to.

Flerbörd

Patient information leaflet

Flerbörd

If you ... Identical twins can look different at birth. Their heads may be different shapes because they were moulded differently by their position in the womb and during labour, and one may be larger than the other. The DNA test for twins is called zygosity determination. You take DNA samples by sweeping a cotton bud inside each baby's mouth. DNA.

Parkinsons sjukdom

Patient information leaflet

Parkinsons sjukdom

However, if you take an MAO-B inhibitor at first, it may delay the need for levodopa for months or years. Sometimes these medicines are used in combination with levodopa in the later stages of PD. Other medicines used for PD Catechol-O-methyltransferase (COMT) inhibitors are relatively new medicines. They include tolcapone , entacapone and.

Genetisk testning

Patient information leaflet

Genetisk testning

Genetisk testing is a type of medical test that identifies changes in chromosomes, genes or proteins. Genetic tests examine a person's DNA in a variety of ways to assess a person's genetic health. They are all designed to identify a particular gene that may cause a genetic disorder. We all have 46 chromosomes in our cells. Chromosomes are made from.

Muskeldystrofi

Patient information leaflet

Muskeldystrofi

What is muscular dystrophy. Muscular dystrophy (MD) is the name given to a group of disorders which cause progressive muscle weakness (meaning it gets worse over time). There are many different types of MD. The different types vary... What causes muscular dystrophy. The cause is an abnormal or 'faulty' gene. Genes are made from a biological.

Åldrande

Patient information leaflet

Åldrande

At some point they reach a stage when they stop dividing, called senescence. Changes (mutations) in the DNA codes (genes) within our cells. It may also be that the presence or absence of certain genes allows people to live longer. With repeated dividing, the telomeres - protective structures at the end of the threads of genes (chromosomes) -.

Vidare läsning och referenser

Artikelhistorik

Informationen på denna sida är skriven och granskad av kvalificerade kliniker.
  • 10 Apr 2023 | Senaste versionen
  • 1 Jul 2017 | Ursprungligen publicerad

Delta i konversationen

Dela dina tankar eller erfarenheter med andra i vår patientgemenskaper.

Ansvarsfriskrivning: The views expressed in the community do not represent medical advice. For any health concerns, consult your GP or healthcare provider.
influensaberättigandekontroll

Fråga, dela, anslut.

Bläddra i diskussioner, ställ frågor och dela erfarenheter inom hundratals hälsorelaterade ämnen.

Anmäl dig till Patientens nyhetsbrev

Din veckovisa dos av tydliga, pålitliga hälsoråd - skrivna för att hjälpa dig känna dig informerad, självsäker och i kontroll.

Vänligen ange en giltig e-postadress

Genom att prenumerera accepterar du våra Sekretesspolicy. Du kan avsluta prenumerationen när som helst. Vi säljer aldrig dina uppgifter.