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1.
Hum Immunol ; 79(7): 530-531, 2018 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-29729321

RESUMEN

We have studied Wiwa/Sanja Amerindians HLA-A, -B, -C, -DRB1 and DQB1 allele frequencies and extended haplotypes in 52 unrelated individuals from "El Encanto" town at Guanachaca riverside. High frequency alleles were in general present in other Amerindian populations. Also, three extended haplotypes and eight ones were respectively both "new found" and already described in Amerindians from North, Central and South America, including Lakota-Sioux, Mayas, Teeneks, Quechua and Aymaras. Analyses of HLA-A*24:02 and -C*01:02 Wiwa high frequency alleles suggested a specific relatedness with another Amerindian and Pacific Islander ethnic groups (these two particular alleles bearing in high frequencies); they include New Zealand Maoris, Taiwanese, Japanese, Papua New Guinea, and Samoans among others. This may indicate that selective forces are maintaining these two alleles high frequency within this wide American/Pacific area.


Asunto(s)
Etnicidad , Antígenos HLA/genética , Indígenas Sudamericanos , Nativos de Hawái y Otras Islas del Pacífico , Colombia , Frecuencia de los Genes , Genotipo , Haplotipos , Prueba de Histocompatibilidad , Humanos , Lingüística , Islas del Pacífico , Filogenia
2.
Hum Immunol ; 79(4): 189-190, 2018 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-29454071

RESUMEN

HLA-A,-B,-C,-DRB1 and -DQB1 alleles have been studied in Chimila Amerindians from Sabana de San Angel (North Colombian Coast) by using high resolution molecular typing. A frequent extended haplotype was found:HLA-A*24:02-B*51:10-C*15:02-BRB1*04:07-DQB1*03:02 (28.7%) which has also been described in Amerinndian Mayos Mexican population (Mexico, California Gulf, Pacific Ocean). Other haplotypes had already been found in Amerindians from Mexico (Pacific and Atlantic Coast), Peru (highlands and Amazon Basin), Bolivia and North USA. A geographic pattern according to HLA allele or haplotype frequencies is lacking in Amerindians, as already known. Also, five new extended haplotypes were found in Chimila Amerindians. Their HLA-A*24:02 high frequencies characteristic is shared with aboriginal populations of Taiwan; also, HLA-C*01:02 high frequencies are found in New Zealand Maoris, New Caledonians and Kimberly Aborigines from Australia. Finally, this study may show a model of evolutionary factors acting and rising one HLA allele frequency (-A*24:02), but not in others that belong to the same or different HLA loci.


Asunto(s)
Frecuencia de los Genes , Antígenos HLA/genética , Indígenas Sudamericanos/genética , Colombia , Haplotipos , Humanos
3.
PLoS One ; 12(1): e0169929, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28114347

RESUMEN

Kurds from Iraq (Dohuk and Erbil Area, North Iraq) have been analyzed for HLA genes. Their HLA genetic profile has been compared with that of other Kurd groups from Iran and Tbilisi (Georgia, Caucasus) and also Worldwide populations. A total of 7,746 HLA chromosomes have been used. Genetic distances, NJ dendrograms and correspondence analyses have been carried out. Haplotype HLA-B*52-DRB1*15 is present in all three analyzed Kurd populations. HLA-A*02-B*51-DRB1*11 is present in Iraq and Georgia Kurds. Haplotypes common to Iran and Iraq Kurds are HLA DRB1*11-DQB1*03, HLA DRB1*03-DQB1*02 and others in a lower frequency. Our HLA study conclusions are that Kurds most probably belong to an ancient Mediterranean / Middle East / Caucasian genetic substratum and that present results and those previously obtained by us in Kurds may be useful for Medicine in future Kurd transplantation programs, HLA Epidemiology (HLA linked diseases) and Pharmacogenomics (HLA-associated drug side effects) and also for Anthropology. It is discussed that one of the most ancient Kurd ancestor groups is in Hurrians (2,000 years BC).


Asunto(s)
Antígenos HLA/genética , Georgia (República) , Haplotipos , Irán , Irak , Filogenia
4.
Mol Immunol ; 44(9): 2426-35, 2007 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-17123606

RESUMEN

Caribbean Islands including Cuba were first inhabited by Meso-American and later by Arawak-speaking Amerindians from nowadays Venezuela. Spanish invaders brought to almost extinction to the Amerindian population after 1492. Black slaves from West Africa were taken into Cuba by Europeans. The degree of admixture among populations is approached. HLA alleles were studied by DNA techniques. Comparison with other worldwide populations (a total of 14.094 chromosomes) included genetic distances, Neighbour-Joining dendrograms, correspondence analyses and calculation of extended haplotypes. While African-European HLA features were clearly found, Amerindian HLA characteristics are less evident, indicating that Amerindian devastation was particularly marked after 1492 AD. However, typical Amerindian alleles have been found in our Cuban sample, i.e. DRB1*0403, DRB1*0404, DRB1*0407, DRB1*0411, DRB1*0802 and DRB1*1602. The presence of Amerindian alleles in Cubans [corrected] may have a bear in the making up of transplantation registries (both for bone marrow and solid organ transplantation) at the regional level and also be important for epidemiological studies of diseases linked to HLA.


Asunto(s)
Alelos , Genes MHC Clase II/genética , Genes MHC Clase I/genética , Indígenas Norteamericanos/genética , Pueblo Asiatico/genética , Población Negra/genética , Cuba/etnología , Frecuencia de los Genes , Geografía , Haplotipos/genética , Humanos , Inuk/genética , Filogenia , Población Blanca/genética
5.
Immunogenetics ; 55(12): 866-72, 2004 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-14985876

RESUMEN

Two theories about MHC allele generation have been put forward: (1) point mutation diversification and/or (2) gene conversion events. A model supporting the existence of both of these mechanisms is shown in this paper; the possible evolution of the HLA-B*570101 and HLA-B*5801 alleles (which belong to the HLA-B17 serology group) is studied. The hypothesis favoured is that gene conversion events have originated these alleles, because intron sequences are also analysed. Evolution by point mutation should only be accepted if flanking introns have also been sequenced.


Asunto(s)
Alelos , Antígenos HLA-B/genética , Intrones/genética , Secuencia de Bases , ADN Complementario , Evolución Molecular , Conversión Génica , Variación Genética , Antígenos HLA-B/clasificación , Humanos , Datos de Secuencia Molecular , Mutación , Homología de Secuencia de Ácido Nucleico , Transducción de Señal
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