|
|
(One intermediate revision by one other user not shown) |
Line 1: |
Line 1: |
| An '''allele''' ({{IPAc-en|uk|ˈ|æ|l|iː|l}} or {{IPAc-en|us|ə|ˈ|l|iː|l}}), or '''allel''', is one of a number of alternative forms of the same [[gene]] or same [[Locus (genetics)|genetic locus]] (generally a group of genes).<ref name="Collins"/><ref name="Basic glossary on genetic epidemiology"/> It is the alternative form of a gene for a character producing different effects. Sometimes different alleles can result in different observable [[phenotypic trait]]s, such as different pigmentation. However, many genetic variations result in little or no observable variation.
| | Obesity is the condition in which the body mass index surpasses the usual amount. Generally folks with BMI exceeding 30 are considered obese. There are certain weight facts which one should be aware of.<br><br>My point is I recognize I'm not overweight and I know I am a healthy person on my cholesterol plus blood stress, so there are elements that give to my weight a calculator can't account for.<br><br>This useful service was invented by a Belgian polymath called, Adolphe Quetelet back inside the 1800s. It has first been called the Quetelet index before being renamed because the BMI. This really is very useful in keeping track of how much fat you may be losing and how much fat we require gain to be fit. Combine this with a diet suitable for the eating habits plus cravings plus exercise and sooner or later you'll own a magnificently fit and healthy body, with a BMI range of best wellness.<br><br>In addition, men commonly have more muscle than women plus ladies have more fat inside their body than guys. For this reason, females should have their weight plus height ratio calculated from a [http://safedietplans.com/bmi-calculator bmi calculator females] for females.<br><br>If you are planning on going to the gym, taking a friend a lengthy can give you the confidence to keep going and the two of you can cheer each alternative on in the fight to burn which fat! Exercising each day is stressful on the body, however. Try doing a usual routine each different day, then in between a 30 walk on the treadmill or ride on the bicycle!<br><br>This means that the query of the perfect fat range for athletic ladies inside their 40's is a tough nut to crack. Your body is the body, regardless what age you're plus regardless what amount of exercise we do. Ladies, if you need to have the body of the 21-year-old, we can do it.<br><br>If you don't fall inside the normal range, then receive oneself checked with different (omit) techniques to figure out the amount of body fat. This might provide a better perspective plus enable we to do or keep up your perfect fat. |
| | |
| Most [[multicellular organism]]s have two sets of [[chromosome]]s, that is, they are [[diploid]]. These chromosomes are referred to as [[homologous chromosome]]s. Diploid organisms have one copy of each gene (and therefore one allele) on each chromosome. If both alleles are the same, they and the organism are [[homozygous]], and the organisms are [[homozygote]]s. If the alleles are different, they and the organism are [[heterozygous]] and the organisms are [[heterozygote]]s.
| |
| | |
| A [[population]] or [[species]] of organisms typically includes multiple alleles at each [[Locus (genetics)|locus]] among various individuals. Allelic variation at a locus is measurable as the number of alleles ([[Polymorphism (biology)|polymorphism]]) present, or the proportion of heterozygotes in the population.
| |
| | |
| For example, at the gene locus for the [[ABO]] [[blood type]] [[carbohydrate]] [[antigen]]s in humans,<ref name="<ref name="OnlineMendelianInheritanceinMan"/> classical genetics recognizes three alleles, I<sup>A</sup>, I<sup>B</sup>, and I<sup>O</sup>, that determine compatibility of [[blood transfusion]]s. Any individual has one of six possible [[genotype]]s (AA, AO, BB, BO, AB, and OO) that produce one of four possible [[phenotype]]s: "A" (produced by AA homozygous and AO heterozygous genotypes), "B" (produced by BB homozygous and BO heterozygous genotypes), "AB" heterozygotes, and "OO" homozygotes. It is now known that each of the A, B, and O alleles is actually a class of multiple alleles with different DNA sequences that produce proteins with identical properties: more than 70 alleles are known at the ABO locus.<ref name="Sequence variation at the human ABO locus"/> An individual with "Type A" blood may be an AO heterozygote, an AA homozygote, or an AA heterozygote with two different "A" alleles.
| |
| | |
| The word "allele" is a short form of [[allelomorph]] ("other form"), which was used in the early days of [[genetics]] to describe variant forms of a [[gene]] detected as different [[phenotypes]]. It derives from the Greek prefix ἀλλήλ- ["allel-"], meaning "reciprocal" or "each other", which itself is related to the Greek adjective ἄλλος (allos; cognate with Latin "alius"), meaning "other".
| |
| | |
| ==Dominant and recessive alleles==
| |
| In many cases, genotypic interactions between the two alleles at a locus can be described as [[Dominance (genetics)|dominant]] or [[recessive]], according to which of the two homozygous genotypes the phenotype of the heterozygote most resembles. Where the heterozygote is indistinguishable from one of the homozygotes, the allele involved is said to be [[Dominance (genetics)|dominant]] to the other, which is said to be [[recessive]] to the former.<ref name="Essential genetics: A genomics perspective"/> The degree and pattern of dominance varies among loci. For a further discussion see [[Dominance (genetics)]]. This type of interaction was first formally described by [[Gregor Mendel]]. However, many traits defy this simple categorization and the phenotypes are modeled by [[Quantitative trait locus|polygenic inheritance]].
| |
| | |
| The term "[[wild type]]" allele is sometimes used to describe an allele that is thought to contribute to the typical phenotypic character as seen in "wild" populations of organisms, such as fruit flies (''[[Drosophila melanogaster]]''). Such a "wild type" allele was historically regarded as dominant, common, and normal, in contrast to "[[mutant]]" alleles regarded as recessive, rare, and frequently deleterious. It was commonly thought that most individuals were homozygous for the "wild type" allele at most gene loci, and that any alternative "mutant" allele was found in homozygous form in a small minority of "affected" individuals, often as [[genetic diseases]], and more frequently in heterozygous form in "[[Genetic carrier|carriers]]" for the mutant allele. It is now appreciated that most or all gene loci are highly polymorphic, with multiple alleles, whose frequencies vary from population to population, and that a great deal of genetic variation is hidden in the form of alleles that do not produce obvious phenotypic differences.
| |
| | |
| ==Allele and genotype frequencies==
| |
| The frequency of alleles in a diploid population can be used to predict the frequencies of the corresponding genotypes (see [[Hardy-Weinberg principle]]). For a simple model, with two alleles:
| |
| | |
| : <math>p + q=1 \, </math> | |
| | |
| : <math>p^2 + 2pq + q^2=1 \,</math>
| |
| | |
| where ''p'' is the frequency of one allele and ''q'' is the frequency of the alternative allele, which necessarily sum to unity. Then, ''p''<sup>2</sup> is the fraction of the population homozygous for the first allele, 2''pq'' is the fraction of heterozygotes, and ''q''<sup>2</sup> is the fraction homozygous for the alternative allele. If the first allele is dominant to the second, then the fraction of the population that will show the dominant phenotype is ''p''<sup>2</sup> + 2''pq'', and the fraction with the recessive phenotype is ''q''<sup>2</sup>.
| |
| | |
| With three alleles:
| |
| | |
| : <math>p + q + r = 1 \, </math> and
| |
| | |
| : <math>p^2 + 2pq + 2pr + q^2 + 2qr + r^2 = 1. \,</math>
| |
| | |
| In the case of multiple alleles at a diploid locus, the number of possible genotypes (G) with a number of alleles (a) is given by the expression:
| |
| | |
| : <math>G= \frac{a(a+1)}{2}. </math>
| |
| | |
| ==Allelic variation in genetic disorders==
| |
| A number of [[genetic disorders]] are caused when an individual inherits two recessive alleles for a single-gene trait. Recessive genetic disorders include [[Albinism]], [[Cystic Fibrosis]], [[Galactosemia]], [[Phenylketonuria]] (PKU), and [[Tay-Sachs Disease]]. Other disorders are also due to recessive alleles, but because the gene locus is located on the X chromosome, so that males have only one copy (that is, they are [[hemizygosity|hemizygous]]), they are more frequent in males than in females. Examples include red-green [[color blindness]] and [[Fragile X syndrome]].
| |
| | |
| Other disorders, such as [[Huntington disease]], occur when an individual inherits only one dominant allele.
| |
| | |
| ==See also==
| |
| {{Portal|Evolutionary biology}}
| |
| * [[Allozyme]]
| |
| * [[Evolution]]
| |
| * [[Genealogical DNA test]]
| |
| * [[Haplo-sufficiency]]
| |
| * [[Meiosis]]
| |
| * [[Mendelian error]]
| |
| * [[Mendelian inheritance]]
| |
| * [[Mitosis]]
| |
| * [[Polymorphism (biology)|Polymorphism]]
| |
| * [[Punnett square]]
| |
| | |
| ==References and notes==
| |
| {{reflist|refs=
| |
| | |
| <ref name="OnlineMendelianInheritanceinMan">{{cite web |url=http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=110300 |title=ABO Glycosyltransferase; ABO |author=Victor A. McKusick, Cassandra L. Kniffin, Paul J. Converse and Ada Hamosh |date=10 November 2009 |work=Online Mendelian Inheritance in Man |publisher=National Library of Medicine |accessdate=24 March 2010|archiveurl = http://www.webcitation.org/5uHmF2xJW |archivedate = 2010-11-16|deadurl=no}}</ref>
| |
| | |
| <ref name="Basic glossary on genetic epidemiology">{{cite journal |author=Malats N, Calafell F |title=Basic glossary on genetic epidemiology |journal=Journal of Epidemiology and Community Health |volume=57 |issue=7 |pages=480–2 |date=July 2003 |pmid=12821687 |pmc=1732526 |url=http://jech.bmj.com/cgi/pmidlookup?view=long&pmid=12821687 |doi=10.1136/jech.57.7.480|archiveurl = http://www.webcitation.org/5uHmH9uTG |archivedate = 2010-11-16|deadurl=no}}</ref>
| |
| | |
| <ref name="Collins">{{cite journal |author=Feero WG, Guttmacher AE, Collins FS |title=Genomic medicine--an updated primer |journal=N. Engl. J. Med. |volume=362 |issue=21 |pages=2001–11 |date=May 2010 |pmid=20505179 |doi=10.1056/NEJMra0907175}}</ref>
| |
| | |
| <ref name="Essential genetics: A genomics perspective">{{cite book |title=Essential genetics: A genomics perspective |edition=4th |last=Hartl |first=Daniel L. |authorlink= |author2=Elizabeth W. Jones |year=2005 |publisher=Jones & Bartlett Publishers |location= |isbn=978-0-7637-3527-2 |oclc= |page=600 |url= |accessdate=5 October 2009}}</ref> | |
| | |
| <ref name="Sequence variation at the human ABO locus">{{cite journal |author=Yip SP |title=Sequence variation at the human ABO locus |journal=Annals of Human Genetics |volume=66 |issue=1 |pages=1–27 |date=January 2002 |pmid=12014997 |doi=10.1017/S0003480001008995}}</ref>
| |
| }}
| |
| * National Geographic Society, Alton Biggs, Lucy Daniel, Edward Ortleb, Peter Rillero, Dinah Zike. "Life Science". New York, Ohio, California, Illinois: Glencoe McGraw-Hill. 2002
| |
| | |
| ==External links==
| |
| * [http://alfred.med.yale.edu/alfred/index.asp ALFRED: The ALlele FREquency Database]
| |
| * [http://www.ehstrafd.org EHSTRAFD.org - Earth Human STR Allele Frequencies Database]
| |
| | |
| [[Category:Classical genetics]]
| |
| [[Category:Genetic genealogy]]
| |
Obesity is the condition in which the body mass index surpasses the usual amount. Generally folks with BMI exceeding 30 are considered obese. There are certain weight facts which one should be aware of.
My point is I recognize I'm not overweight and I know I am a healthy person on my cholesterol plus blood stress, so there are elements that give to my weight a calculator can't account for.
This useful service was invented by a Belgian polymath called, Adolphe Quetelet back inside the 1800s. It has first been called the Quetelet index before being renamed because the BMI. This really is very useful in keeping track of how much fat you may be losing and how much fat we require gain to be fit. Combine this with a diet suitable for the eating habits plus cravings plus exercise and sooner or later you'll own a magnificently fit and healthy body, with a BMI range of best wellness.
In addition, men commonly have more muscle than women plus ladies have more fat inside their body than guys. For this reason, females should have their weight plus height ratio calculated from a bmi calculator females for females.
If you are planning on going to the gym, taking a friend a lengthy can give you the confidence to keep going and the two of you can cheer each alternative on in the fight to burn which fat! Exercising each day is stressful on the body, however. Try doing a usual routine each different day, then in between a 30 walk on the treadmill or ride on the bicycle!
This means that the query of the perfect fat range for athletic ladies inside their 40's is a tough nut to crack. Your body is the body, regardless what age you're plus regardless what amount of exercise we do. Ladies, if you need to have the body of the 21-year-old, we can do it.
If you don't fall inside the normal range, then receive oneself checked with different (omit) techniques to figure out the amount of body fat. This might provide a better perspective plus enable we to do or keep up your perfect fat.