How is height genetically determined
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Anthropometric measurements of the Hungarian twins were supported by Medexpert Ltd. Buchwald, PI. Jacob v. Patrik K. Magnusson, Nancy L. Maria A. Wendy Cozen, Amie E. Jane Wardle, Clare H. Tom A. McAdams, Thalia C. Robert F. Margaret Gatz, Laura A. Meike Bartels, Toos C. You can also search for this author in PubMed Google Scholar. All authors have commented the manuscript and read and approved the final version of the manuscript. This work is licensed under a Creative Commons Attribution 4.
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Provided by the Springer Nature SharedIt content-sharing initiative. Height is often inherited — but the precise genetics factors have long eluded researchers.
You need only to look at families to see that height is inherited — and studies of identical twins and families have long confirmed that suspicion.
Studies seeking the genes that govern height have identified hundreds of common gene variants linked to the trait. The case of the missing heritability. Now, a study suggests that most of the missing heritability for height and body mass index BMI can, as some researchers had suspected, be found in rarer gene variants that had lain undiscovered until now. To seek out the genetic factors that underlie diseases and traits, geneticists turn to mega-searches known as genome-wide association studies GWAS.
These scour the genomes of, typically, tens of thousands of people — or, increasingly, more than a million — for single-letter changes, or SNPs, in genes that commonly appear in individuals with a particular disease or that could explain a common trait such as height. But GWAS have limitations. In turn, these , common variants would have been found from sequencing the genomes of just a few hundred people, says Timothy Frayling, a human geneticist at the University of Exeter, UK.
They turned to whole-genome sequencing — performing a complete readout of all 6 billion bases — of 21, people. The authors declined to comment on the preprint, because it is under submission at a journal. They relied on the simple, but powerful, principle that all people are related to some extent — albeit distantly — and that DNA can be used to calculate degrees of relatedness.
As a result, the researchers captured genetic differences that occur in only 1 in , or even 1 in 5,, people. And by using information on both common and rare variants, the researchers arrived at roughly the same estimates of heritability as those indicated by twin studies.
Ensuring good nutrition during pregnancy is also important for the bone health and growth of the fetus. Sleep promotes growth and development in children and teenagers. During deep sleep, the body releases the hormones it needs to grow. Getting enough sleep may therefore allow optimal growth. Regular exercise is also important for normal physical development.
Playing outside or taking part in sports, for example, can make bones healthier, denser, and stronger. Babies and children grow continuously. This is due to changes in the growth plates in the long bones of their arms and legs. People grow the fastest in the first 9 months of life, before being born.
After birth, this slows down. Once a child is 8 years old, they will grow at an average of 2. After this, the growth plates stop making new bone, and the person will stop growing. The hands and feet stop growing first, then the arms and legs. The last area to stop growing is the spine. Scientists have identified more than different genes that determine height. Some of these genes affect the growth plates, and others affect the production of growth hormones. Normal height ranges are different for people from different ethnic backgrounds.
Again, this is determined by their DNA. Males tend to be taller than females. Males may also continue growing for longer than females. On average, an adult male is 5. Learn about what age girls stop growing and what age boys stop growing here. Once a person has been through puberty, the growth plates stop making new bone.
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