Name: tracing traits with pedigree charts
Uploaded: 2021-04-07T12:11:58.000Z
Duration: 1 min 35 s
Channel: JoVE

K12 Standards

north-carolina-k-12-science-standard-course-of-study

North Carolina K-12 Science Standard Course of Study

9-12

Biology

heredity-inheritance-and-variation-of-traits

Heredity- Inheritance and Variation of Traits

LS.Bio.7.1

Pedigree Analysis

Um zu verstehen, wie Merkmale oder Störungen beim Menschen vererbt werden, analysieren Wissenschaftler Stammbäume.
 In einem typischen Stammbaum bezeichnen Quadrate Männchen, Kreise Weibchen und eine horizontale Linie zwischen diesen Formen eine Paarung.
 Wenn eine solche Vereinigung Kinder hervorbringt, wird eine senkrechte Linie von den Eltern zu allen Söhnen und Töchtern gezogen, so dass zunehmend niedrigere Reihen im Stammbaum nachfolgende Generationen in einer Familie darstellen.
 Bei Individuen, die einen erkrankten Phänotyp aufweisen, wie Hautausschläge im Zusammenhang mit einer Biotinidase-Mangelstörung, bei denen das für die Gewinnung von Vitamin B7 erforderliche Enzym fehlt, sind die zugehörigen Formen im Stammbaum mit Schattierungen versehen.
 Durch die Beurteilung, bei welchen Familienmitgliedern ein Biotinidase-Mangel diagnostiziert wurde, können Forscher feststellen, ob diese Krankheit auf einer rezessiven oder dominanten Mutation in einem einzelnen Gen auf einem Autosom oder Geschlechtschromosom beruht.
 Hier sind Frauen und Männer gleich häufig betroffen.
 Nicht betroffene Eltern haben Kinder mit der Störung und nicht jede Generation enthält ein Familienmitglied mit der Krankheit.
 Ein Muster, das auf einen Biotinidase-Mangel hindeutet, ist autosomal-rezessiv.
 Wichtig ist, dass die Stammbaumanalyse nicht nur die Vererbungsmuster aufklärt, sondern auch Paare dabei unterstützt, das Risiko zu verstehen, dass sie aufgrund ihrer Familienanamnese ein Kind mit dieser Störung haben.
 Risiko eines betroffenen Kindes

Chial, Heidi. 2008. "Mendelsche Genetik: Vererbungsmuster und Einzelgenstörungen." Nature Education 1 (1): 63. [<a href="https://www.nature.com/scitable/topicpage/mendelian-genetics-patterns-of-inheritance-and-single-966" target="__blank">Quelle</a>]

Germain, Dominique P. 2006. "Allgemeine Aspekte von X-chromosomalen Krankheiten." In Morbus Fabry: Perspektiven aus 5 Jahren FOS, herausgegeben von Atul Mehta, Michael Beck und Gere Sunder-Plassmann. Oxford: Oxford PharmaGenesis. [<a href="https://www.ncbi.nlm.nih.gov/books/NBK11593/" target="__blank">Quelltext</a>]

stammbaum-analyse

<h4>Überblick</h4>
 
 Ein Stammbaum ist ein Diagramm, welcher die Geschichte eines Merkmals in einer Familie darstellt. Die Analyse von Stammbäumen kann (1) zeigen, ob ein Merkmal dominant oder rezessiv ist, (2) den Typ des Chromosoms, autosomal oder geschlechtsbestimmend, mit dem ein Merkmal verbunden ist, (3) Genotypen von Familienmitgliedern und (4) Wahrscheinlichkeiten von Phänotypen in zukünftigen Generationen vorhersagen. Für Familien mit einer Geschichte von autosomalen oder Geschlechtsabhängigen Krankheiten können diese Informationen für die Familienplanung entscheidend sein.
 
 <h4> Stammbäume zeigen Familiengeschichten </h4>
 
 Bei verschiedenen Pflanzen -und Tierarten untersuchen die Wissenschaftler die Vererbung von Phänotypen oder Merkmalen mit Hilfe von sorgfältig kontrollierten Paarungsexperimenten, sogenannten Kreuzungen. Beispielsweise können reinerbige Kreuzungen eine Merkmalsdominanz oder Rezessivität etablieren. Testkreuzungen können beispielsweise den Genotyp (homozygot oder heterozygot) eines Organismus mit einem bekannten dominanten Phänotyp bestimmen.
 
 Aus ethischen und praktischen Gründen werden Menschen nicht gekreuzt. Deshalb analysieren Forscher Stammbäume, oder auch Familienstammbäume, um zu verstehen, wie menschliche Eigenschaften und Krankheiten vererbt werden. Stammbäume zeigen die Geschichte eines Merkmals über Generationen und Familienmitglieder hinweg. Unter Verwendung derselben Prinzipien, die für Kreuzungen gelten, können Informationen über die Vererbung eines Merkmals abgeleitet werden.
 
 <h4>Die Reihen eines Stammbaums repräsentieren die Generationen einer Familie</h4>
 
 In einem typischen Stammbaum repräsentieren Quadrate männliche Individuen und Kreise weibliche Individuen. Schattierte Quadrate oder Kreise bedeuten, dass ein zu untersuchendes Merkmal in einem Individuum vorkommt. Die Reihen stellen Generationen dar und sind manchmal mit römischen Zahlen versehen. Die älteste Generation ist in der obersten Zeile, wobei jede nachfolgende Generation in einer darunter folgenden Zeile steht. Innerhalb jeder Generation oder Zeile können die Familienmitglieder von links nach rechts numerisch unterteilt werden und durch ihre Generation und Position bestimmt werden. Zum Beispiel wird das zweite Individuum in der ersten Generation mit I-2 bezeichnet.
 
 Eine horizontale Linie, welche zwei Elternteile verbindet, wird als Ehelinie bezeichnet. Der eigentliche Akt der Ehe ist hier unwesentlich. Eine vertikal absteigende Linie, die sich von einer Ehelinie nach unten erstreckt, verbindet sich mit einer horizontalen Geschwisterlinie. Personen, die über die Geschwisterlinie mit der Abstammungslinie verbunden sind, sind Nachkommen. Individuen, die nicht direkt mit der Geschwisterlinie verbunden sind, sind über die Ehelinie in die Familie eingetreten und sind keine biologischen Nachkommen der vorhergehenden Generation.
 
 <h4>Stammbäume geben Informationen über die Vererbung von Merkmalen und Krankheiten frei</h4>
 
 Dominante Merkmale sind anders verteilt als rezessive Merkmale. Die Vererbung ist auch bei Merkmalen, die durch Gene auf Geschlechtschromosomen bestimmt werden, im Vergleich zu Merkmalen, die an Autosomen gebunden sind (Nicht-geschlechtsbestimmende Chromosomen), unterschiedlich. Durch die Untersuchung des Vorhandenseins und der Abwesenheit eines Merkmals in einer Familie kann die Stammbaumanalyse Informationen über die Vererbung von Merkmalen liefern. Obwohl viele Krankheiten von mehreren Genen beeinflusst werden, zeigen mehrere Mendelsche Vererbungsmuster. Für diese Erkrankungen können Stammbäume wichtige Hinweise auf das Risiko der Vererbung und Ausbreitung von Krankheiten liefern.
 
 Merkmale, die durch Gene auf Nicht-geschlechtsbestimmenden Chromosomen verursacht werden und zwei Allelkopien benötigen, um einen Phänotyp zu beeinflussen, sind autosomal rezessiv. Etliche Erkrankungen sind autosomal rezessiv. Dazu gehören z.B. Mukoviszidose, Tay-Sachs-Krankheit und die Ahornsirupkrankheit. Die meisten Menschen mit diesen Erkrankungen haben heterozygote Eltern, die nicht die Erkrankung haben, aber ein kausales Allel tragen.
 
 Diese Träger können die Krankheit unwissentlich an ihre Kinder weitergeben, was teilweise erklärt, warum autosomal rezessive Erkrankungen häufiger vorkommen, als ihre dominanten Gegenstücke. Der Vergleich von Generationen in einem Stammbaum kann zeigen, ob ein autosomales Merkmal dominant oder rezessiv ist. Wenn keiner der beiden Elternteile hat das Merkmal, aber ein Kind erbt es, muss also rezessiv sein.
 
 Sommersprossen und Polydaktylie (zusätzliche Finger oder Zehen) sind autosomal dominante Merkmale beim Menschen, die nur eine Kopie des bestimmenden Allels benötigen, um den Phänotyp zu beeinflussen. Autosomal dominante Krankheiten, wie z.B. die Huntingtons-Krankheit, betreffen ~50% der Nachkommen bei einem betroffenen Elternteil. Viele dieser Krankheiten verursachen erst später im Leben Symptome, oft erst nach dem reproduktiven Alter. Kinder können diese Krankheiten von unwissentlich betroffenen Eltern erben, was die Bedeutung der Analyse der Familiengeschichte unterstreicht. Obwohl beide Elternteile diese Eigenschaft aufweisen, ist eines ihrer Kinder nicht betroffen. Da eine Kreuzung zwischen zwei rezessiven Eltern immer einen rezessiven Phänotyp hervorbringt, muss dieses Merkmal dominant sein.
 
 <h4>Merkmale können autosomal oder geschlechtsgebunden sein</h4>
 
 Zusätzlich zu 44 Nicht-geschlechtsbestimmenden Chromosomen hat der Mensch zwei Geschlechtschromosomen, die bei Frauen (XX) homolog sind, bei Männern aber nicht homolog (XY). Die durch die Geschlechtschromosomen bestimmten Merkmale sind geschlechtsgebunden. Die meisten geschlechtsgebundenen Merkmale beim Menschen sind X-gebunden rezessiv. Nur Männer können Y-gebundene Merkmale erben, da den Frauen ein Y-Chromosom fehlt. Zusätzlich enthält das X-Chromosom ~800-900 proteincodierende Gene im Vergleich zu ~70-80 auf dem Y-Chromosom.
 
 X-gebundene Merkmale sind Hämophilie, Muskeldystrophie und Rot-Grün-Farbblindheit. Da Männer nur ein X-Chromosom haben, sind sie hemizygot (und nicht homozygot oder heterozygot) für ein X-gebundenes Merkmal. Männer sind anfälliger für rezessive X-chromosomale Merkmale als Frauen, da sie kein zweites Allel haben, das ein kausal rezessives Allel möglicherweise verdeckt.

Stammbaum-Analyse

Überblick

Ein Stammbaum ist ein Diagramm, das die Vorgeschichte eines Merkmals in einer Familie zeigt. Die Analyse von Stammbäumen kann Aufschluss darüber geben, (1) ob ein Merkmal dominant ist oder ...

Education

Lehre

JoVE Core

Molecular Biology

Molekularbiologie

Unit 2

Einheit 2

Mendelian Genetics

Mendelsche Genetik

KEY TERMS AND CONCEPTS

KERNBEGRIFFE UND KONZEPTE

tracing traits with pedigree charts

Pedigree analysis uses family trees, called pedigrees, to trace how traits and diseases pass from one generation to the next. A pedigree chart helps scientists and students see inheritance patterns clearly across relatives.

The chart uses standard symbols to show family members and their relationships. It can reveal whether a trait is likely passed through dominant or recessive inheritance, and it can also help identify patterns linked to sex chromosomes.

By studying a pedigree, it is possible to follow a trait through multiple generations and compare affected and unaffected individuals. This makes pedigree analysis a useful tool for understanding genetic inheritance and for predicting how a trait may appear in future family members.

Tracing Traits with Pedigree Charts

punnett squares

Predicting Traits with Punnett Squares

Punnett squares help students predict how traits may be passed from parents to offspring. They are a simple grid used in genetics to organize possible allele combinations. An allele is a version of a gene. The square compares the alleles each parent can give. By filling in the boxes, students can see possible genotypes, which are the genetic makeup of offspring. The results can also help connect those genotypes to traits that may appear in the next generation.

monohybrid crosses

Tracking One Trait in Monohybrid Crosses

Monohybrid crosses track how one trait is passed from parents to offspring. They are used to study inheritance when only a single characteristic is followed at a time. A monohybrid cross can compare the possible outcomes for a monogenic trait, which is a trait controlled by one gene. This approach helps show how one gene can shape different inherited forms of the same characteristic. The method also connects with Mendel's work on genetics. It is a useful way to predict patterns of inheritance...

dihybrid crosses

Predicting Two-Trait Genetic Crosses

Dihybrid crosses are used to predict how two traits can be passed from parents to offspring. A dihybrid cross tracks two genes at the same time, so it helps students see how different alleles can combine in a genetic pattern. This topic is closely tied to Mendelian genetics and independent assortment. Independent assortment means that allele pairs for different traits can separate into gametes independently of one another. When students work through a dihybrid cross, they can compare the...

trihybrid crosses

Forked Line Method for Trihybrid Crosses

Forked line method for trihybrid crosses helps predict the outcome of three-trait Mendelian crosses. A trihybrid cross studies three pairs of contrasting characteristics. It combines three separate monohybrid crosses. Common examples include plant height, seed shape, and seed color. In a typical trihybrid cross, the F1 plants are heterozygous for all three traits. They can produce eight different gametes. After self-fertilization, these gametes can lead to 64 genotype combinations in the F2...

law of independent assortment

Independent Chromosome Assortment in Meiosis

Independent chromosome assortment in meiosis explains how different gene pairs can be inherited independently. This idea is one of Mendel’s laws of inheritance and is often called the law of independent assortment. The pattern depends on how homologous chromosomes line up during meiosis I. Each chromosome pair orients independently of the others, so the maternal and paternal chromosomes can separate into different gametes in many combinations. This random separation helps create genetic...

chi-square analysis

Chi-Square Test in Genetics

The chi-square test in genetics helps compare expected and observed results. It is a statistical hypothesis test used to see whether a difference between an expected value and an observed value is significant. In genetics, it helps decide whether to accept or reject a hypothesis based on how far the observed data moves from the expected data. The test was developed by Pearson in 1990. The first step is to set up a null hypothesis. This hypothesis says there is no real difference between the...

pedigree analysis

Pedigree analysis uses family trees, called pedigrees, to trace how traits and diseases pass from one generation to the next. A pedigree chart helps scientists and students see inheritance patterns clearly across relatives. The chart uses standard symbols to show family members and their relationships. It can reveal whether a trait is likely passed through dominant or recessive inheritance, and it can also help identify patterns linked to sex chromosomes. By studying a pedigree, it is...

multiple allele traits

Multiple Alleles in Trait Inheritance

Multiple alleles can shape how a trait is inherited in a population. A gene may have more than two allele forms, even though each person still carries only two alleles for that gene. These allele combinations can produce traits with more than two possible outcomes. The ABO blood group system is a common example of a multiple allele trait. It shows how different alleles can interact to determine an organism’s phenotype, or observable trait. Multiple allele traits help explain why inheritance...

incomplete dominance

Incomplete Dominance in Traits and Disease

Incomplete dominance is a pattern of inheritance where two alleles both affect a trait in a heterozygous organism. In this case, one allele is not fully dominant over the other. The result is a phenotype that looks like a blend or intermediate form. Gregor Mendel’s pea plant experiments helped explain the usual dominant and recessive pattern. He showed that each gene in a diploid cell has two alleles, one inherited from each parent. In his model, a dominant allele shows its effect with one or...

lethal alleles

When Genes Cause Embryonic Death

Lethal alleles can change inheritance patterns by causing death before birth. In mice, Lucien Cuénot studied the agouti gene, which helps control coat color through an agouti-signaling protein that affects melanin distribution in mammals. The wild-type allele produces a gray-brown coat, while the mutant allele produces a yellow coat. Cuénot also found that the yellow allele was linked to yellow mouse obesity syndrome. This syndrome is associated with early-onset obesity and tumors. When he...

polygenic traits

Traits Shaped by Many Genes

Polygenic traits are characteristics shaped by many genes acting together. This pattern is different from a single-gene trait, where one gene has a larger effect on the outcome. In polygenic inheritance, each gene adds a small contribution to the final trait. Height is a common example of a polygenic trait. Many genes influence human height, so the result can vary across a wide range. These small genetic effects combine to produce differences that are easy to see in a population. Polygenic...

background and environment affect phenotype

background-and-environment-affect-phenotype

How Genes and Environment Shape Traits

Genes and the environment work together to shape phenotype, or the visible traits of an organism. A phenotype can change because of genetic background, environmental conditions, or both. Factors such as temperature, oxygen availability, and mutagens can all influence how a trait appears. Horses show how one gene can affect coat color and how a modifier gene can change that result. The Extension gene controls pigment production in the coat. The wild-type genotype EE produces black pigment,...

x and y chromosomes

Sex Chromosomes in Human Inheritance

Sex chromosomes help determine biological sex in mammals, including humans. Humans have two sex chromosomes, X and Y. Each diploid cell has 22 pairs of autosomes and one pair of sex chromosomes. A female usually has two X chromosomes, while a male usually has one X chromosome and one Y chromosome. Egg and sperm cells carry only half the usual number of chromosomes. They contain 22 autosomes and one sex chromosome. Every egg has an X chromosome. Sperm cells can carry either an X or a Y...

the y chromosome determines maleness

Y Chromosome Structure and Male Traits

The Y chromosome is a sex chromosome that helps guide male development in humans and other vertebrates and mammals. Human males usually have one X chromosome and one Y chromosome, along with 22 pairs of autosomes. In these organisms, the presence or absence of the Y chromosome influences whether male traits develop. The Y chromosome evolved from an autosome about 300 million years ago, when two sex chromosomes began to diverge. Since then, it has lost most of its genes and become much smaller.

the ratio of x chromosome to autosomes

Drosophila Sex Determination by X:A Balance

In Drosophila, sex is determined by the balance between X chromosomes and autosomes, not by the X and Y chromosomes alone. The Y chromosome is active in these flies, but it does not set sex. Instead, it carries genes needed for sperm production in adult males. A normal male Drosophila has one X chromosome and two sets of autosomes. A normal female has two X chromosomes and two sets of autosomes. When this X:A ratio changes, flies can develop different sexual phenotypes, including metamales,...

x-linked traits

X-Linked Inheritance in Families

X-linked inheritance in families explains how traits linked to the X chromosome pass from parents to children. These traits are often tracked through family trees because the pattern can differ between males and females. A male has one X chromosome and one Y chromosome. A female has two X chromosomes. Because of this difference, a trait on the X chromosome can show up in a different way depending on the sex of the child. Family examples often include traits such as color blindness. Studying...

sex linked disorders

Sex-Linked Disorders and Inheritance Patterns

Sex-linked disorders are genetic conditions that follow inheritance patterns tied to the sex chromosomes. These disorders help explain how certain traits can appear more often in one sex than the other. The transcript focuses on examples of sex-linked disorders, including Y-linked infertility, Fragile X syndrome, and Duchenne muscular dystrophy. Y-linked infertility is passed through the Y chromosome, while Fragile X syndrome and Duchenne muscular dystrophy are associated with sex-linked...

dosage compensation

X-Chromosome Balance in Animals

X-chromosome balance in animals helps equalize gene expression between males and females. Sex can be determined by the number and type of sex chromosomes. In humans, females have two X chromosomes and males have one X and one Y chromosome. In C. elegans, one X chromosome is male, while two X chromosomes make a hermaphrodite. The X chromosome carries more than sex-related genes. It also includes genes involved in body functions such as brain development and the immune system. Because males and...

x-inactivation

X-Inactivation and Barr Bodies

X-inactivation is a process that reduces gene activity on one X chromosome. It helps balance gene expression in cells that have more than one X chromosome. A key result of this process is the formation of a Barr body, which is the inactive X chromosome seen in the nucleus. This topic also includes Xist, a gene linked to X-inactivation. Xist produces RNA that coats the X chromosome and helps turn it off. Together, Xist and the Barr body show how cells control X-linked genes during development...

blood types

Blood Types and Transfusion Matching

Human blood types help determine safe blood transfusion matching. Blood is classified by antigens on the surface of red blood cells and antibodies in the plasma. Correct blood typing matters because an unsafe match can affect transfusion success. The International Society of Blood Transfusion has identified 38 human blood types, and ABO, Rh, and MNS are among the most common. The ABO blood group depends on antigens made by genes on chromosome 9. Red blood cells carry a base glycoprotein called...

blood transfusion and agglutination

Matching Blood Types for Safe Transfusion

Blood transfusion is a medical treatment used to restore blood volume after major blood loss from an accident or a medical procedure. It works by taking blood from a suitable donor and giving it to a recipient. Safe transfusion depends on matching blood types and checking for immune compatibility. The history of blood transfusion began in the 17th century, when early experiments were done in animals. In 1818, James Blundell, a British doctor, performed the first successful human blood...

key terms and concepts

Learn how pedigree charts track traits and diseases across generations, showing inheritance patterns such as dominant, recessive, and sex-linked traits.

Tracing Traits with Pedigree Charts | JoVE K12

molecular biology

JoVE Core Molecular Biology veranschaulicht die molekularen Prozesse der Zelle in prägnanten animierten Video-Lektionen. In Videos von Wissenschaftlern in Aktion wird die Anwendung dieser Konzepte zusätzlich durch reale Experimente in modernen Laboren demonstriert.

Louisiana Student Standards for Science

High School

Life Sciences

Heredity: Inheritance And Variation Of Traits

HS-LS3-1

ohios-learning-standards-and-model-curriculum

Ohio’s Learning Standards and Model Curriculum

Heredity

Genetic mechanisms and inheritance

Alabama Course of Study Science

Heredity: Inheritance and Variation of Traits

9-12.B.3.11

Florida Department of Education

Life Science

SC.912.L.16

SC.912.L.16.2

Texas Essential Knowledge and Skills

BIO.8

BIO.8.B

myJoVE Corporation

What is Meiosis?

Meiosis is the process by which diploid cells divide to produce haploid daughter cells. In humans, each diploid cell contains 46 chromosomes, half from ...

Meiosis I

Meiosis II

Meiosis vs. Mitosis

Crossing Over

Crossing over is the exchange of genetic information between homologous chromosomes during prophase I of meiosis I. Genetic recombination gives rise to ...

Nondisjunction

Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This ...

Spermatogenesis

Spermatogenesis is the process by which haploid sperm cells are produced in the male testes. It starts with stem cells located close to the outer rim of ...

Oogenesis

In human women, oogenesis produces one mature egg cell or ovum for every precursor cell that enters meiosis. This process differs in two unique ways from ...

Fertilization

During fertilization, an egg and sperm cell fuse to create a new diploid structure. In humans, the process occurs once the egg has been released from the ...

Cleavage and Blastulation

After a large-single-celled zygote is produced via fertilization, the process of cleavage occurs while zygotes travel through the uterine tube. Cleavage ...

Gastrulation

Gastrulation establishes the three primary tissues of an embryo: the ectoderm, mesoderm, and endoderm. This developmental process relies on a series of ...

Neurulation

Neurulation is the embryological process which forms the precursors of the central nervous system and occurs after gastrulation has established the three ...

Cell Migration

Cell migration, the process by which cells move from one location to another, is essential for the proper development and viability of organisms ...

Determination

During embryogenesis, cells become progressively committed to different fates through a two-step process: specification followed by determination. ...

Use models to explain how DNA is passed from parents to offspring through the processes of meiosis and fertilization in sexual reproduction.

LS.Bio.6.1

Mutations

Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations ...

genome-size-and-the-evolution-of-new-genes

Genome Size and the Evolution of New Genes

types-of-genetic-transfer-between-organisms

Types of Genetic Transfer Between Organisms

Base-pairing and DNA Repair

The DNA Replication Fork

Lagging Strand Synthesis

The Replisome

Proofreading

Synthesis of new DNA molecules is carried out by the enzyme DNA polymerase, which adds nucleotides on the daughter strand complementary to the template ...

Replication in Prokaryotes

DNA replication has three main steps: initiation, elongation, and termination. Replication in prokaryotes begins when initiator proteins bind to the ...

Replication in Eukaryotes

In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before ...

Overview of DNA Repair

Base Excision Repair

Nucleotide Excision Repair

DNA Distortion and Damage
Cells are regularly exposed to mutagens&#8212;factors in the environment that can damage DNA and generate mutations. UV ...

Mismatch Repair

Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the ...

Fixing Double-strand Breaks

Homologous Recombination

Gene Conversion

Restarting Stalled Replication Forks

Construct an explanation to summarize how inheritable genetic variations may result from: new genetic combinations in meiosis, mutations during replication, or mutations caused by environmental factors.

LS.Bio.6.2

An Overview of Genetic Analysis

An organism&#8217;s physical traits, or phenotype, are a product of its genotype, which is the combination of alleles (gene variants) inherited from its ...

Genetic Crosses

To dissect genetic processes or create organisms with novel suites of traits, scientists can perform genetic crosses, or the purposeful mating of two ...

Punnett Squares

Monohybrid Crosses

Dihybrid Crosses

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 Independent Assortment

Chi-square Analysis

The chi-square test is a statistical hypothesis test. It is used to check whether there is a significant difference between an expected value and an ...

Multiple Allele Traits

Incomplete Dominance

Gregor Mendel&#39;s work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid ...

Lethal Alleles

Agouti: A Lethal Allele
Lucien Cu&#233;not discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is ...

Polygenic Traits

Background and Environment Affect Phenotype

Although the genetic makeup of an organism plays a major role in determining the phenotype, there are also several environmental factors, such as ...

Use mathematics and computational thinking to predict the variation and distribution of expressed traits based on: Mendelian inheritance, co-dominance, incomplete dominance, multiple alleles, and sex-linked inheritance.

Overview

A pedigree is a diagram displaying a family&#x2019;s history of a trait. Analyzing pedigrees can reveal (1) whether a trait is dominant or ...

Probability Laws

Overview

The probability of inheriting a trait can be calculated using the sum and product rules. The sum rule is used to calculate the probability of ...

The Concept of Multiple Allelism

Multiple allelism describes genes that exist in three or more allelic forms. Although diploid organisms, like humans, ...

Analyze and interpret data to explain how polygenic traits result in a wide range of phenotypes.

LS.Bio.7.2

Pleiotropy

Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause ...

Construct an explanation to summarize how traits result from interactions of genetic factors (multiple genes and/or alleles) and environmental factors.

LS.Bio.7.3

Understand genetic mechanisms for variation.

Tracing Traits with Pedigree Charts

Description

Transcript

Tags

More videos by Standards