globalchange  > 过去全球变化的重建
DOI: 10.1111/joim.12878
WOS记录号: WOS:000471324100006
论文题名:
Nutrition and its role in human evolution
作者: James, W. P. T.1; Johnson, R. J.2; Speakman, J. R.3; Wallace, D. C.4; Fruhbeck, G.5; Iversen, P. O.6; Stover, P. J.7
通讯作者: James, W. P. T.
刊名: JOURNAL OF INTERNAL MEDICINE
ISSN: 0954-6820
EISSN: 1365-2796
出版年: 2019
卷: 285, 期:5, 页码:533-549
语种: 英语
英文关键词: genetics ; human evolution ; nutrition
WOS关键词: AMINO-ACID BALANCE ; LACTASE PERSISTENCE ; LYSINE REQUIREMENTS ; NATURAL-SELECTION ; GENE CONVERSION ; JEBEL IRHOUD ; POLYMORPHISMS ; ADAPTATION ; CHIMPANZEE ; ORIGINS
WOS学科分类: Medicine, General & Internal
WOS研究方向: General & Internal Medicine
英文摘要:

Our understanding of human evolution has improved rapidly over recent decades, facilitated by large-scale cataloguing of genomic variability amongst both modern and archaic humans. It seems clear that the evolution of the ancestors of chimpanzees and hominins separated 7-9million years ago with some migration out of Africa by the earlier hominins; Homo sapiens slowly emerged as climate change resulted in drier, less forested African conditions. The African populations expanded and evolved in many different conditions with slow mutation and selection rates in the human genome, but with much more rapid mutation occurring in mitochondrial DNA. We now have evidence stretching back 300000years of humans in their current form, but there are clearly four very different large African language groups that correlate with population DNA differences. Then, about 50000-100000years ago a small subset of modern humans also migrated out of Africa resulting in a persistent signature of more limited genetic diversity amongst non-African populations. Hybridization with archaic hominins occurred around this time such that all non-African modern humans possess some Neanderthal ancestry and Melanesian populations additionally possess some Denisovan ancestry. Human populations both within and outside Africa also adapted to diverse aspects of their local environment including altitude, climate, UV exposure, diet and pathogens, in some cases leaving clear signatures of patterns of genetic variation. Notable examples include haemoglobin changes conferring resistance to malaria, other immune changes and the skin adaptations favouring the synthesis of vitamin D. As humans migrated across Eurasia, further major mitochondrial changes occurred with some interbreeding with ancient hominins and the development of alcohol intolerance. More recently, an ability to retain lactase persistence into adulthood has evolved rapidly under the environmental stimulus of pastoralism with the ability to husband lactating ruminants. Increased amylase copy numbers seem to relate to the availability of starchy foods, whereas the capacity to desaturase and elongate monounsaturated fatty acids in different societies seems to be influenced by whether there is a lack of supply of readily available dietary sources of long-chain polyunsaturated fatty acids. The process of human evolution includes genetic drift and adaptation to local environments, in part through changes in mitochondrial and nuclear DNA. These genetic changes may underlie susceptibilities to some modern human pathologies including folate-responsive neural tube defects, diabetes, other age-related pathologies and mental health disorders.


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资源类型: 期刊论文
标识符: http://119.78.100.158/handle/2HF3EXSE/137927
Appears in Collections:过去全球变化的重建

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作者单位: 1.London Sch Hyg & Trop Med, Keppel St, London WC1E 7HT, England
2.Univ Colorado, Div Renal Dis & Hypertens, Denver, CO 80202 USA
3.Chinese Acad Sci, Inst Genet & Dev Biol, Beijing, Peoples R China
4.Childrens Hosp Philadelphia, Res Inst, Mitochondrial & Epigen Med, Philadelphia, PA 19104 USA
5.Clin Univ Navarra, Endocrinol & Nutr, Pamplona, Spain
6.Univ Oslo, Dept Nutr, Oslo, Norway
7.Texas A&M AgriLife, Agr & Life Sci, College Stn, TX USA

Recommended Citation:
James, W. P. T.,Johnson, R. J.,Speakman, J. R.,et al. Nutrition and its role in human evolution[J]. JOURNAL OF INTERNAL MEDICINE,2019-01-01,285(5):533-549
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