Pregled bibliografske jedinice broj: 191899
Mutations that modulate receptor-hormone congruency as a cause of the primate GH receptor species specifity
Mutations that modulate receptor-hormone congruency as a cause of the primate GH receptor species specifity // Theory in biosciences, 123 (2005), 435-440 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 191899 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Mutations that modulate receptor-hormone congruency as a cause of the primate GH receptor species specifity
Autori
Kurbel, Sven ; Gulam, Danijela ; Kovačić, Damir ; Mihaljević, Ivan ; Faj, Dario
Izvornik
Theory in biosciences (1431-7613) 123
(2005);
435-440
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Growth hormone/genetics ; mutation ; phylogeny ; species specifity
Sažetak
Peptide hormones depend on reliable recognition by their receptors. Any mutation that compromises recognition of hormone and receptor molecules is dangerous, the carrier animal would not procreate and the mutation would be lost. Although most of the hormones from one mammalian species are active when injected into another, the incompatibility of human GH receptor (GHR) toward non primate GHs is a notable exception. It is reported that the coevolution of GH and GHR in primates includes two crucial steps (Liu JC et al. Mol. Biol. Evol. 2001 ; 18:945-53.). The first was mutation of GH His->Asp at position 171 that happened before the split of Old world and New world monkeys. The second event was Leu->Arg change at position 43 in the GH receptor molecule that happened in the ancestor of Old world monkeys. The proposed model is based on the possibility that certain mutations can modify the surface of one of interacting molecules to form a confined empty space, a niche in the otherwise congruent hormone/receptor interface. Although affinity between molecules is probably slightly reduced, recognition and function are not compromised in this special case. Further mutations of hormone and receptor molecules are allowed under the condition that they remain confined to the niche space. Mutations that do not compromise hormone function can be passed to offsprings. If the consequent mutation of one molecule change its shape to fill the niche space, further mutations without function loss will become less probable. Without the niche space, the phase of fast evolution is closed and both genes become conserved. In this setting, accumulated mutations before the niche closing mutation are the cause of species specifity. To become a dominant variety, carrier animals must possess survival advantage in comparison to the carriers of other less advantageous mutations.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
0127051
Ustanove:
Klinički bolnički centar Osijek
Profili:
Sven Kurbel
(autor)
Ivan Mihaljević
(autor)
Damir Kovačić
(autor)
Dario Faj
(autor)
Danijela Gulam
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE