Mitoferrin-1

Mitoferrin-1 is a protein that in humans is encoded by the SLC25A37 gene. It is a member of the solute carrier family 25. Mitoferrin-1 is primarily located in the mitochondria, where it plays a crucial role in iron homeostasis and heme biosynthesis.

Function

Mitoferrin-1 is an iron transporter that is essential for the synthesis of heme and iron-sulfur (Fe-S) clusters. It facilitates the uptake of iron into the mitochondria, where it is used in the production of heme and Fe-S clusters. These are vital components of many proteins, including those involved in oxygen transport, energy production, and DNA repair.

Clinical significance

Mutations in the SLC25A37 gene that encodes Mitoferrin-1 can lead to various medical conditions. For instance, a deficiency in Mitoferrin-1 can result in microcytic anemia, a condition characterized by smaller than normal red blood cells. This is due to the reduced heme synthesis, which is necessary for the production of hemoglobin, the protein in red blood cells that carries oxygen.

Research

Research into Mitoferrin-1 has potential implications for the treatment of diseases such as iron deficiency anemia and mitochondrial disease. Understanding the function and regulation of Mitoferrin-1 could lead to new therapeutic strategies for these conditions.

See also

• Solute carrier family
• Mitochondria
• Heme
• Microcytic anemia
• Iron deficiency anemia
• Mitochondrial disease

References

‎

---

Translate: - East Asian 中文, 日本, 한국어, South Asian हिन्दी, தமிழ், తెలుగు, Urdu, ಕನ್ನಡ, Southeast Asian Indonesian, Vietnamese, Thai, မြန်မာဘာသာ, বাংলা
European español, Deutsch, français, Greek, português do Brasil, polski, română, русский, Nederlands, norsk, svenska, suomi, Italian
Middle Eastern & African عربى, Turkish, Persian, Hebrew, Afrikaans, isiZulu, Kiswahili,
Other Bulgarian, Hungarian, Czech, Swedish, മലയാളം, मराठी, ਪੰਜਾਬੀ, ગુજરાતી, Portuguese, Ukrainian