Name: how genes map to chromosomes
Uploaded: 2019-08-01T09:31:10.000Z
Duration: 1 min 39 s
Channel: JoVE

K12 Standards

Next Generation Science Standards

High School

Life Science

heredity-inheritance-and-variation-of-traits

Heredity: Inheritance and Variation of Traits

HS-LS3-1

Chromosomal Theory of Inheritance

- [Narratore] Alla fine del 1800,

dopo che Mendel aveva
fatto le sue osservazioni

sull'ereditarietà nelle piante
di pisello, i miglioramenti

nella microscopia
permisero agli scienziati

di visualizzare strutture sub-cellulari

in dettaglio per la prima volta.

Dopo che il processo di mitosi
e meiosi furono osservati

e descritti, è stato proposto

che i cromosomi erano le
particelle ereditabili di Mendel.

La teoria cromosomica dell'eredità

descrive come il comportamento
fisico dei cromosomi

spiega le leggi di segregazione di Mendel

e l'assortimento indipendente.

Gli organismi che si
riproducono sessualmente

hanno due copie di ciascun
cromosoma nelle loro cellule

somatico, o non riproduttive.

Durante la meiosi, coppie
omologhe di cromosomi,

quelli che portano gli
stessi geni, sono divise

e segregate nei gameti
in modo che ogni gamete

riceva una copia di ogni
cromosoma, proprio come Mendel

descrisse nella sua legge di segregazione.

Le coppie cromosomiche
diverse, o non omologhe,

non sono legate tra loro

e si dividono nei gameti
in modo indipendente,

come descritto nella legge di Mendel

sull'assortimento indipendente.

Dopo la fecondazione, i gameti combinano

il loro materiale genetico per generare

un organismo con due
copie di ciascun cromosoma

e quindi, due copie di ciascun gene,

uno ereditato dalla madre e uno dal padre,

proprio come Mendel aveva
predetto in base agli schemi

di eredità che studiò
nelle piante di pisello.

Miko, I. (2008) Thomas Hunt Morgan e il legame sessuale. Educazione alla natura 1(1):143. [<a href="https://www.nature.com/scitable/topicpage/thomas-hunt-morgan-and-sex-linkage-452">Sorgente</a>]

Gayon, Jean. 2016. "Da Mendel all'epigenetica: storia della genetica". Comptes Rendus Biologies 339 (7-8): 225–30. [<a href="https://doi.org/10.1016/j.crvi.2016.05.009">Sorgente</a>]

teoria cromosomica dell'ereditarietà

Nel 1866, Gregor Mendel pubblicò i risultati dei suoi esperimenti di allevamento di piante di piselli, fornendo prove per modelli prevedibili nell'eredità delle caratteristiche fisiche. Il significato delle sue scoperte non è stato immediatamente riconosciuto. Infatti, l'esistenza dei geni era sconosciuta all'epoca. Mendel si riferiva alle unità ereditarie come "fattori".

I meccanismi alla base delle osservazioni di Mendel, alla base delle sue leggi di segregazione e assortimento indipendente, rimasero sfuggenti. Alla fine del 1800, i progressi nelle tecniche di microscopia e colorazione hanno permesso agli scienziati di visualizzare la mitosi e la meiosi per la prima volta.

Nei primi anni del 1900, Theodor Boveri, Walter Sutton e altri proponevano indipendentemente che i cromosomi possano essere alla base delle leggi di Mendel, la teoria cromosomica dell'eredità. La ricerca di ricci di mare e cavallette, rispettivamente, Boveri e Sutton hanno notato sorprendenti somiglianze tra i cromosomi durante la meiosi e i fattori di Mendel.

Come i fattori di Mendel, i cromosomi sono disponibili in coppia. Ricordando la legge di segregazione di Mendel, queste coppie si separano durante la meiosi in modo che ogni gamete (ad esempio, sperma o uovo) riceva un cromosoma da ogni coppia. Le coppie cromosomiche sono separate indipendentemente l'una dall'altra, corrispondente alla legge di Mendel di assortimento indipendente.

Le prime prove concrete per la teoria cromosomica dell'eredità provenivano da uno dei suoi critici, Thomas Hunt Morgan. Morgan scoprì che una mutazione che influenzava il colore degli occhi dei moscerini della frutta era ereditata in modo diverso dalle mosche maschili e femminili, e dimostrò che questo tratto era determinato dal cromosoma X.

Ora sappiamo che i fattori di Mendel sono segmenti di DNA, chiamati geni, in posizioni cromosomiche specifiche. L'assortimento indipendente di geni su cromosomi diversi è una conseguenza della disposizione casuale dei cromosomi alla linea mediana di una cellula durante la metafase I, che determina quali geni si segregano nelle stesse cellule figlie. Ogni coppia omologa di cromosomi migra indipendentemente dagli altri. La legge della segregazione corrisponde al movimento dei cromosomi durante l'anafase I che assicura, in condizioni normali, che ogni gamete riceva solo una copia di ogni cromosoma distribuito in modo casuale.

Teoria cromosomica dell'ereditarietà

In 1866, Gregor Mendel published the results of his pea plant breeding experiments, providing evidence for predictable patterns in the inheritance of ...

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Biology

Biologia

Genetics

Genetica

Classical and Modern Genetics

Genetica classica e moderna

KEY TERMS AND CONCEPTS

TERMINI E CONCETTI CHIAVE

how genes map to chromosomes

Genes map to chromosomes, and this idea explains how Mendel’s inheritance patterns work. Gregor Mendel published his pea plant breeding results in 1866. He showed that physical traits follow predictable patterns. At the time, scientists did not yet know that genes existed. Mendel used the word &quot;factors&quot; for the hereditary units he studied.

The details behind Mendel’s laws of segregation and independent assortment were still unknown for many years. In the late 1800s, better microscopes and staining methods let scientists see mitosis and meiosis for the first time. These advances gave researchers a way to study how hereditary material behaves in cells. The chromosomal theory of inheritance grew from this work in the early 1900s.

Theodor Boveri and Walter Sutton independently suggested that chromosomes could explain Mendel’s laws. Boveri studied sea urchins, and Sutton studied grasshoppers. They saw that chromosomes during meiosis looked much like Mendel’s factors. Chromosomes also come in pairs, just as Mendel’s factors do. During meiosis, paired chromosomes separate so each gamete, such as a sperm or egg, receives one chromosome from each pair. Chromosome pairs also separate independently from one another, matching Mendel’s law of independent assortment.

Strong evidence came from Thomas Hunt Morgan, who had been a critic of the theory. He studied a fruit fly eye color mutation and found that it was inherited differently in males and females. This showed that the trait was linked to the X chromosome. We now know that Mendel’s factors are DNA segments called genes, and each gene sits at a specific place on a chromosome. The random arrangement of chromosome pairs at metaphase I affects which genes end up in the same daughter cells, and anaphase I helps ensure that each gamete gets one copy of each chromosome under normal conditions.

How Genes Map to Chromosomes

genetic lingo

Genotype, Phenotype, and Inheritance

Genotype, phenotype, and inheritance help explain how traits and disease risk are passed from parents to offspring. In diploid organisms, including humans, most other animals, and many plants, somatic cells carry a duplicate set of chromosomes. These chromosome pairs are homologous, with similar length, centromere position, and gene locations. Diploid organisms inherit two versions of each gene, one from each parent. These versions are called alleles, and they sit at the same relative locus,...

punnett squares

Punnett Squares for Predicting Traits

Punnett squares help predict which traits offspring may inherit from two parents. They show possible genotypes, which are pairs of alleles, and can also show the chance of a phenotype, or visible trait, when the inheritance pattern is known. These grids work best for traits controlled by a single gene locus and passed on independently during meiosis. Punnett squares were developed in the early 1900s by Reginald Punnett. His work came after Gregor Mendel’s pea plant experiments revealed the...

monohybrid crosses

Mendel’s Pea Plant Inheritance Ratios

Gregor Mendel used pea plants to study how traits are passed from parents to offspring. His breeding experiments in the 1850s and 1860s showed that inheritance follows clear patterns. He crossed true-breeding plants that differed in one trait and found that dominant traits can hide recessive traits. Mendel focused on seven pea plant traits, and each trait had two forms controlled by a single gene locus. He noticed that true-breeding plants always produced offspring with the same phenotype, or...

dihybrid crosses

Mendel's Law of Independent Assortment

Mendel’s law of independent assortment explains how two traits can be inherited separately. Gregor Mendel tested this idea with pea plants that differed in two characteristics, such as pea color and pea shape. He used true-breeding parents that were homozygous for both traits but showed different phenotypes. In one example, Mendel crossed round, yellow peas with wrinkled, green peas. The parental generation had RRYY and rryy genotypes. Their first-generation offspring were all dihybrids,...

law of segregation

Mendel’s Pea Cross Ratios

Mendel’s pea plant crosses show how traits can disappear in one generation and return in the next. When he crossed plants, one parental trait sometimes seemed to vanish in the F1 generation and reappear in the F2 generation. Mendel used this pattern to explain why some traits are dominant and others are recessive. He proposed that traits are controlled by alleles, which are different versions of a gene. An organism inherits two copies of each gene, one from each parent. In his model, a...

law of independent assortment

Mendel’s Dihybrid Cross and Trait Ratios

Mendel’s dihybrid cross shows how two traits are inherited at the same time. A dihybrid cross is a cross in which both parents are homozygous for two distinct traits, and the F1 generation is heterozygous for both traits. Mendel used pea plants with round yellow peas and wrinkled green peas as an example. One parent had genotype YYRR, and the other had genotype yyrr. In the F1 generation, every plant showed the dominant traits, so the plants were YyRr and had yellow, round peas. The F2...

probability laws

Inheritance Risk with Sum and Product Rules

Inheritance risk can be calculated with the sum rule and the product rule. The sum rule applies to mutually exclusive events, or events that cannot happen at the same time. The product rule applies to independent events, or events that do not affect one another. These rules describe theoretical probability, which is the chance of an event before it happens. Empirical probability is different because it is based on events that have already occurred. These probability rules are useful in...

test cross

Using Test Crosses to Identify Genotypes

Test crosses are used to identify the genotype of an organism with a dominant trait. A genotype is the pair of alleles inherited for a gene, and alleles are different forms of the same gene. In diploid organisms, including humans, each gene usually has two alleles, one from each parent. An allele is recessive when its effect is hidden by another allele at the same gene location. Pea plants provide a clear example with flower color. White flowers are recessive, because one copy of the purple...

pedigree analysis

Reading Family Traits in Pedigrees

Pedigrees are family trees used to track how a trait passes through generations. They help scientists and students see whether a trait is dominant or recessive, whether it is autosomal or sex-linked, what genotypes family members may have, and what phenotypes may appear in future generations. For families with a history of inherited disease, this information can be important for family planning. In plants and animals, inheritance is often studied with crosses. Monohybrid crosses can show...

polygenic traits

Polygenic Traits in Human Height

Polygenic traits are traits controlled by more than one gene. Human height is a clear example of this kind of inheritance. Because many genes work together, the final trait can vary a lot from person to person. Researchers have found hundreds of loci, or gene locations, that influence height. There are likely many more that have not yet been identified. Many of these genes affect cartilage in the growth plates of the long bones in the arms and legs, either directly or indirectly. Height is...

multiple allele traits

Blood Type and Allele Interactions

Multiple alleles can shape traits through blood type, sickle cell anemia, incomplete dominance, and codominance. Multiple allelism means a gene has three or more allelic forms. Diploid organisms, including humans, usually carry only two alleles for each gene, but many human genes exist in multiple forms in the population. Human blood type is a clear example of multiple allelism. The blood type gene has three alleles: I A , I B , and i. These alleles help determine which blood type a person has...

epistasis

Gene Masking in Rabbit Fur Color

Epistasis describes how one gene can mask or change the effect of another gene. In high school genetics, this helps explain why many traits do not follow a simple single-gene pattern. Instead, alleles at different locations can work together to shape the final phenotype. Mendel studied seven unrelated pea traits, but most traits involve multiple gene interactions. Epistasis often happens when one gene interferes with the expression of another gene. It can also occur when genes are part of the...

nature and nurture

Genes and Environment Shape Height

Genes and environment both shape human height and other traits. Genes are the inherited instructions we get from our parents. Environment includes factors such as diet, stress, and social conditions. Many phenotypes, or observable traits, reflect both influences. Some also show up later in life, including cancer and other diseases. Height is a clear example of this interaction. Scientists estimate that 70-90% of height variation comes from genetic differences among people. The remaining 10-30%...

pleiotropy

SOX10 and Multiple Traits in Pleiotropy

Pleiotropy is when one gene affects more than one trait. The SOX10 gene is a clear example because it can influence pigmentation, hearing, and intestinal movement. These traits may seem unrelated, but they can all be linked to the same gene change. In humans, a deleted region in SOX10 can cause Waardenburg Syndrome Type 4, or WS4. WS4 is an autosomal recessive disorder, which means a person usually inherits two altered copies of the gene. Common signs include a white forelock,...

sex-linked disorders

X- and Y-Linked Disorder Patterns

X- and Y-linked disorders come from mutations in genes on the sex chromosomes. These genes, like those on autosomes, are needed for normal body function. When a mutation causes a biological problem, the condition is called sex-linked. Y-linked disorders come from changes in the Y chromosome. They affect only males, because only males carry a Y chromosome. Mutations in this small chromosome can affect male sexual function and secondary sex characteristics. One example is Y-chromosome...

x-linked traits

X-Linked Inheritance in Families

X-linked inheritance explains how traits on the X chromosome are passed through families. In most mammalian species, females have two X sex chromosomes, while males have one X and one Y. A mutation on one X chromosome may be masked in females by a normal allele on the other X. In males, that same mutation is more likely to show because there is no second normal X to balance it. Traits caused by changes on the X chromosome are called X-linked traits. Color blindness is a well-studied example.

x-inactivation

Barr Bodies and X-Chromosome Balance

Barr bodies and X-chromosome balance help explain how female mammalian cells control gene activity from the X chromosome. The human X chromosome carries far more genes than the Y chromosome. Because males usually have one X chromosome and females have two, females would make twice as many of some proteins without a control system. To prevent that imbalance, female mammalian cells inactivate nearly all the genes on one X chromosome during early embryonic development. The inactive X condenses...

non-nuclear inheritance

Maternal DNA in Mitochondria and Chloroplasts

Maternal DNA in mitochondria and chloroplasts explains how some genes are inherited outside the nucleus. Most DNA is in the nucleus, but mitochondria and chloroplasts in the cell cytoplasm also carry their own DNA and can copy it independently of nuclear DNA. Mitochondria are found in both plant and animal cells. They are called the powerhouses of eukaryotic cells because they break down glucose to make energy for cellular activity. Mitochondrial DNA has about 37 genes, and many help with...

chromosomal theory of inheritance

Genes map to chromosomes, and this idea explains how Mendel’s inheritance patterns work. Gregor Mendel published his pea plant breeding results in 1866. He showed that physical traits follow predictable patterns. At the time, scientists did not yet know that genes existed. Mendel used the word "factors" for the hereditary units he studied. The details behind Mendel’s laws of segregation and independent assortment were still unknown for many years. In the late 1800s, better microscopes and...

key terms and concepts

Trace how Mendel’s factors became genes on chromosomes, and see how meiosis, segregation, and independent assortment explain inheritance in fruit flies and other organisms.

How Genes Map to Chromosomes | JoVE K12

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new-york-state-science-learning-standards

New York State Science Learning Standards

Inheritance and Variation of Traits

HS-LS3-1.

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Histone Variants at the Centromere

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Inheritance of Chromatin Structures

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Euchromatin

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REF and WEF Fly Genetics
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Genetic Lingo

Overview

An organism is diploid if it inherits two variants, or alleles, of each gene, one from each parent. These two alleles constitute the genotype ...

Punnett Squares

Overview

A Punnett square displays the possible genotypes offspring can inherit from two parental genotypes. If a trait&#x2019;s inheritance pattern ...

Monohybrid Crosses

Overview

In the 1850s and 1860s, Gregor Mendel investigated inheritance by performing monohybrid crosses in pea plants. He crossed two plants that were ...

Dihybrid Crosses

Overview

To determine whether traits are inherited together or separately, Gregor Mendel crossed pea plants that differed in two traits. These parental ...

Trihybrid Crosses

Trihybrid Crosses
Some of Mendel&#8217;s crosses examined three pairs of contrasting characteristics. Such a cross is called a trihybrid cross. A ...

Law of Segregation

When crossing pea plants, Mendel noticed that one of the parental traits would sometimes disappear in the first generation of offspring, called the F1 ...

Law of Independent Assortment

While Mendel&#x2019;s Law of Segregation states that the two alleles for one gene are separated into different gametes, a different question of how ...

Test Cross

Alleles are different forms of the same gene. Humans and other diploid organisms inherit two alleles of every gene, one from each parent.

An allele is ...

Chi-square Analysis

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Pedigree Analysis

Overview

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Nature and Nurture

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Probability Laws

Overview

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Background and Environment Affect Phenotype

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Multiple Allele Traits

The Concept of Multiple Allelism

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X and Y Chromosomes

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The Y Chromosome Determines Maleness

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Non-nuclear Inheritance

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The Ratio of X Chromosome to Autosomes

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Incomplete Dominance

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X-linked Traits

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Lethal Alleles

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Sex-linked Disorders

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Epistasis

In addition to multiple alleles at the same locus influencing traits, numerous genes or alleles at different locations may interact and influence ...

X-Inactivation

The human X chromosome contains over ten times the number of genes as in the Y chromosome. Since males have only one X chromosome, and females have two, ...

Polygenic Traits

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Dosage Compensation

In animals, gender is determined by the number and type of sex chromosome. For example, human females have two X chromosomes, and males have one X and one ...

Pleiotropy

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Ask questions to clarify relationships about the role of DNA and chromosomes in coding the instructions for characteristic traits passed from parents to offspring. [Assessment Boundary: Assessment does not include the phases of meiosis or the biochemical mechanism of specific steps in the process.]

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Meiosis II

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Make and defend a claim based on evidence that inheritable genetic variations may result from (1) new genetic combinations through meiosis, (2) viable errors occurring during replication, and or (3) mutations caused by environmental factors. [Clarification Statement: Emphasis is on using data to support arguments for the way variation occurs.] [Assessment Boundary: Assessment does not include the phases of meiosis or the biochemical mechanism of specific steps in the process.]

HS-LS3-2

How Genes Map to Chromosomes

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