Evidence map›Paper›PMID 27030145›Full record

ArticleJournal of human genetics2016

New native South American Y chromosome lineages.

Marilza S Jota, Daniela R Lacerda, José R Sandoval, Pedro Paulo R Vieira, Dominique Ohasi, José E Santos-Júnior, Oscar Acosta, Cinthia Cuellar, Susana Revollo, Cesar Paz-Y-Miño and 9 more

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In one paragraph

Article in Journal of human genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Marilza S JotaDepartamento de Biologia Geral, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Daniela R LacerdaDepartamento de Biologia Geral, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
José R SandovalDepartamento de Biologia Geral, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Pedro Paulo R VieiraDepartamento de Biologia Geral, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Dominique OhasiDepartamento de Biologia Geral, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
José E Santos-JúniorDepartamento de Biologia Geral, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Oscar AcostaInstituto de Genética y Biología Molecular, Universidad San Martin de Porres, Lima, Peru.
Cinthia CuellarFacultad de Bioquímica, Universidad Mayor de San Andrés, La Paz, Bolivia.
Susana RevolloFacultad de Bioquímica, Universidad Mayor de San Andrés, La Paz, Bolivia.
Cesar Paz-Y-MiñoInstituto de Investigaciones Biomédicas, Universidad de las Americas, Quito, Ecuador.
Ricardo FujitaInstituto de Genética y Biología Molecular, Universidad San Martin de Porres, Lima, Peru.
Gustavo A VallejoUniversidad del Tolima, Ibagué, Colombia.
Theodore G SchurrDepartment of Anthropology, University of Pennsylvania, Philadelphia, PA, USA.
Eduardo M Tarazona-SantosDepartamento de Biologia Geral, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Sergio Dj PenaDepartamento de Bioquímica e Imunologia, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Qasim AyubThe Wellcome Trust Sanger Institute, Hinxton, UK.
Chris Tyler-SmithThe Wellcome Trust Sanger Institute, Hinxton, UK.
Fabrício R SantosDepartamento de Biologia Geral, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Genographic Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many single-nucleotide polymorphisms (SNPs) in the non-recombining region of the human Y chromosome have been described in the last decade. High-coverage sequencing has helped to characterize new SNPs, which has in turn increased the level of detail in paternal phylogenies. However, these paternal lineages still provide insufficient information on population history and demography, especially for Native Americans. The present study aimed to identify informative paternal sublineages derived from the main founder lineage of the Americas-haplogroup Q-L54-in a sample of 1841 native South Americans. For this purpose, we used a Y-chromosomal genotyping multiplex platform and conventional genotyping methods to validate 34 new SNPs that were identified in the present study by sequencing, together with many Y-SNPs previously described in the literature. We updated the haplogroup Q phylogeny and identified two new Q-M3 and three new Q-L54*(xM3) sublineages defined by five informative SNPs, designated SA04, SA05, SA02, SA03 and SA29. Within the Q-M3, sublineage Q-SA04 was mostly found in individuals from ethnic groups belonging to the Tukanoan linguistic family in the northwest Amazon, whereas sublineage Q-SA05 was found in Peruvian and Bolivian Amazon ethnic groups. Within Q-L54*, the derived sublineages Q-SA03 and Q-SA02 were exclusively found among Coyaima individuals (Cariban linguistic family) from Colombia, while Q-SA29 was found only in Maxacali individuals (Jean linguistic family) from southeast Brazil. Furthermore, we validated the usefulness of several published SNPs among indigenous South Americans. This new Y chromosome haplogroup Q phylogeny offers an informative paternal genealogy to investigate the pre-Columbian history of South America.Journal of Human Genetics advance online publication, 31 March 2016; doi:10.1038/jhg.2016.26.

Indexed as

Chromosomes, Human, YGenetics, PopulationAllelesEvolution, MolecularGenotypeHaplotypesHigh-Throughput Nucleotide SequencingHumansIndians, South AmericanMicrosatellite RepeatsMutationPolymorphism, Single Nucleotide

Identifiers

PMID27030145

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.