Name: genome size and gene evolution
Uploaded: 2023-04-30T18:28:42.000Z
Duration: 3 min 21 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.6.2

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

Genome Size and the Evolution of New Genes

رغم بساطة طبيعة الشفرة الجينية هناك اختلاف كبير من حيث حجم الجينوم من الأصغر و المعروف بالجينوسوم التى تتضمن البروتيوباكتيريا كانديداتوس كارسونيلا التى أنصاف اقطارها أقل من 160.000 زوج من القواعد إلى اكبرها, مثل النبات المزهر اليابانى باريس جابونيكا يبلغ حوالي 150 مليار. على الرغم من هذا الاختلاف الشديد البكتيريا والعتائق عندها حوالي 3000 جين داخل جينوماتهم لأن بدائيات النوى تقريبا لا توجد لديها تسلسلات غير مشفرة هذا يعني ان الجينومات الخاصة بهم تكون صغيرة نسبيًا مقارنة بأولئك من حقيقيات النوى. الجينوم الاصفر أيضا يعني الاقل فى الاستنساخ في كل دورة من دورات انقسام الخلايا والذى له معنى لوجستي للتكاثر السريع حقيقيات النوى إجمالا بها تقريبا 20000جين ولكن جينوماتها تتخللها امتدادات طويلة التسلسل غير مشفرة مما يعني ان حجم الجينوم الخاص بهم ليس بالضرورة أن يترجم الى شىء معقد جينوم باريس جابونيكا قد يكون أكبر 50 مرة من حجم جينوم الإنسان, لكن هذا يرجع على الأقل جزئيًا إلى كميات كبيرة من التسلسل غير المشفر وربما مستويات عالية من التكرار ليس بالضرورة المزيد من الجينات الجديدة.

فكيف إذن تُطور الكائنات الحية جينات جديدة؟الجواب عادة بواسطة تعديل التسلسل الذى هو موجود أصلا. أحد الموارد الأساسية لتطور جينات جديدة هو من خلال التكرار الجينيى تخيل قسم من الحمض النووي يحتوى على جين تكرر بطريق الخطأ. الآن الكائن الحي لديه نسخة ثانية من الجين الموجود.

هذه النسخ الجينية الجديدة حرة من القيود الموضوعة على الأصل للحفاظ على الوظيفة وهكذا يستطيعون ان يتنوعوا, ومن المحتمل يحدث تطوير دور جديد أو تعديل لوظيفة أصلية طريقة أخرى لخلق جينات جديدة هي خلط دى إن أيه حيث أجزاء من جين موجود او من نسخة جين يتم فصلها والانتقال للانضمام لأجزاء من جين مختلف صانعا بذلك جين هجين يمكن أن يقوم بوظيفة جديدة الطفرة داخل الجين هى التغييرات في تسلسل الجينات المدمجة عن طريق الطفرات بمرور الوقت وهذه تفسر العديد من الجينات الجديدة هذا التنوع هو الأكثر وضوحا عند مقارنة الأنواع أو الأنساب التي تتنوع بشكل مستقل. بمجرد أن يكون هذا التنوع وراء نقطة معينة أو جين واحد يقوم بوظيفة جديدة يمكن تصنيفها على أنها جينات مختلفة تمامًا. أخيرًا النقل الافقى للجينات يجلب جينات وتسلسلات جديدة إلى الجينوم من مصادر خارجية مثل الأفراد الآخرين وحتى الأنواع الأخرى.

هذا النوع من الجينات الجديدة المكتسبة هو الأكثر شيوعًا في بدائيات النوى والعتائق مع النقل للجينات مقاومة المضادات الحيوية كونه مثالًا معروفًا. بينما نادر في حقيقيات النوى انها لا تزال تُعتبر مصدر أساسي للجينات الجديدة والمواد الجينية يمكن أن تأتي من انواع بعيدة الصلة مثل البكتيريا والفطريات في هذا المثال.

حجم الجينوم وتطور الجينات الجديدة

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في حين أن كل كائن حي لديه جينوم من نوع ما (سواء كان RNA أو DNA)، إلا أن هناك تباينًا كبيرًا في أحجام هذه المخططات. أحد العوامل الرئيسية التي تؤثر على حجم الجينوم هو ما إذا كان الكائن الحي بدائي النواة أو حقيقي النواة. في بدائيات النوى، يحتوي الجينوم على القليل من التسلسل غير المشفر أو لا يحتوي على أي تسلسل، بحيث تتجمع الجينات بإحكام في مجموعات أو مشغلات بشكل تسلسلي على طول الكروموسوم. وعلى العكس من ذلك، فإن الجينات الموجودة في حقيقيات النوى تتخللها فترات طويلة من التسلسل غير المشفر. بشكل عام، يساهم هذا في ظاهرة أن جينومات بدائيات النوى تميل إلى أن تكون أصغر (أي تحتوي على عدد أقل من القواعد) في المتوسط من جينومات حقيقيات النوى.

ومن غير المستغرب، في ضوء هذه الملاحظة، أن أصغر الجينومات المعروفة هي في الغالب بدائيات النوى. على سبيل المثال، تعد كانديداتوس كارسونيلا رودي (Candidatus Carsonella rudii) من البكتيريا البروتينية المبسطة للغاية والتي يبلغ حجم جينومها 160 ألف زوج قاعدي فقط. بعد أن فقدت العديد من الجينات التي كانت بحاجة إليها لتصنيع البروتينات الأساسية للحياة، تطورت لتصبح متكافلة إلزامية داخل الخلايا. وفي الطرف المقابل من الطيف، يعد النبات الزهري الياباني حقيقي النواة باريس جابونيكا واحدًا من أكبر الجينومات المعروفة، حيث يضم حوالي 150 مليار زوج قاعدي. على الرغم من أن عدد الجينات التي يشفرها هذا غير معروف، إلا أن الجينوم يُظهر كميات هائلة من التكرار والتسلسل غير المشفر.

يوجد داخل جينوم بدائيات النوى المتوسطة ما يقرب من 3000 جين. يبلغ متوسط عدد حقيقيات النوى في مكان ما حوالي 20000. لكن حجم الجينوم، وخاصة في حقيقيات النوى، متغير بشكل كبير - ويرجع ذلك إلى حد كبير إلى كمية التسلسل غير المشفر.

خلق جينات جديدة

من أجل تطوير جينات جديدة، لدى الكائنات الحية عدد قليل من الخيارات الرئيسية. الشيء الوحيد المشترك بين معظم هذه العناصر هو أنها تقوم بتعديل التسلسلات الموجودة بالفعل.

يلعب التضاعف دورًا مهمًا في تكوين جينات جديدة، وهناك أنواع قليلة من التضاعف التي يمكن أن تؤدي إلى هذه التسلسلات الجديدة. في ازدواج الجينات، يتم تكرار جزء من الحمض النووي الذي يحتوي على الجين. هذه النسخة الثانية لا تواجه ضغط الاختيار الذي يقيد الأولى، وبالتالي يمكن أن تتباعد. وبمرور الوقت، يمكن أن يؤدي هذا إلى تطور جينات جديدة لها أدوار جديدة.

هناك نوع آخر من التضاعف - خلط الحمض النووي - يمكن أن يؤدي إلى تكرار جزء فقط من الجين وانضمامه إلى جين آخر. وهذا يمكن أن يؤدي إلى خلق جينات جديدة، مع منتجات جديدة.

في بعض الأحيان تتطور الجينات الجديدة ببساطة من الطفرات المتراكمة مع مرور الوقت. يُعرف هذا بالطفرة داخل الجينات، ويكون أكثر وضوحًا عند المقارنة بين الأنواع أو المجموعات المتباينة.

وأخيرا، من الممكن أيضا الحصول على جينات جديدة من مصادر خارجية، في عملية تعرف باسم نقل الجينات الأفقي. وهذا يعني أنه يمكن دمج المادة الوراثية من أفراد آخرين، وأحيانًا من نفس النوع، ولكن من المحتمل أيضًا أن تكون من نوع آخر تمامًا. وهذا مصدر متكرر للجينات الجديدة في بدائيات النوى والعتائق. وهو أقل شيوعًا في حقيقيات النوى، ولكن ثبت حدوثه، ويمكن لحقيقيات النوى حتى التقاط المعلومات الوراثية من مصادر بعيدة مثل البكتيريا أو الفطريات.
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في حين أن كل كائن حي لديه جينوم من نوع ما (سواء كان الحمض النووي الريبي أو الحمض النووي) ، إلا أن هناك تباينا كبيرا في أحجام هذه المخططات. تخصص واحد ...

Education

JoVE Core

Cell Biology

بيولوجيا الخلية

Unit 1

الوحدة الأولى

Cells, Genomes, and Evolution

الخلايا والجينومات والتطور

KEY TERMS AND CONCEPTS

المصطلحات والمفاهيم الأساسية

genome size and gene evolution

Genome size and gene evolution are linked through changes in DNA sequence and genome structure. Some genes can arise from parts of the genome that were not coding before, while others come from changes to existing genes. These shifts help explain how new genetic material can appear over time.

A genome is the full set of DNA in an organism. Its size can change as DNA is added, removed, or rearranged. The transcript highlights that genome size is not fixed, and that these changes can shape the evolution of new genes.

New genes may form by duplication and later change, or by other alterations in noncoding DNA. Over time, these changes can give rise to new functions. This process helps connect genome structure with the emergence of genetic novelty.

Genome Size and Gene Evolution

what are cells?

Cells as the Building Blocks of Life

Cells are the basic building blocks of life. A bacterium can be a single cell, while a human is made of trillions of cells. Even with this range, cells share key features that support life. A living cell has a plasma membrane. This is a bilayer of lipids that separates the cytoplasm inside the cell from the outside environment. A cell also carries genetic information in the form of DNA. In prokaryotic cells, DNA is found in a region called the nucleoid. In eukaryotic cells, DNA is enclosed...

the tree of life - bacteria, archaea, and eukaryotes

the-tree-of-life-bacteria-archaea-and-eukaryotes

Three Domains on the Tree of Life

The tree of life shows how living things are grouped into three domains: Bacteria, Archaea, and Eukaryotes. This classification helps explain the major branches of life and how they are related. Bacteria and Archaea are both single-celled organisms, but they are not the same. Eukaryotes include organisms with more complex cells, such as plants, animals, and fungi. Together, these three domains give a broad picture of life on Earth. Understanding the tree of life helps students compare cell...

prokaryotic cells

How Prokaryotes Survive Without a Nucleus

Prokaryotes are small unicellular organisms that live without a nucleus. They include the domains Archaea and Bacteria. Bacteria include common microbes such as Salmonella and E. coli, while Archaea include extremophiles that live in harsh places like volcanic springs. Prokaryotic cells still share several basic features with eukaryotic cells. They have a plasma membrane, cytoplasm, ribosomes, and genetic material in the form of single, circular DNA. Their cell parts float freely in the...

eukaryotic compartmentalization

How Organelles Keep Cells Working

Eukaryotic cells keep their organelles separate so each part can do a specific job. Organelles such as the nucleus and mitochondria are surrounded by membranes. These membranes are selectively permeable, which means they control what enters and leaves. That control creates small internal environments with conditions suited to each organelle. These controlled spaces help organelles work more efficiently. In animal cells, lysosomes keep an acidic environment that helps their enzymes digest...

eukaryotic evolution

How Eukaryotic Cells Became Complex

Eukaryotic cells became complex through a debated evolutionary path that likely involved endosymbiosis. The most accepted model is the endosymbiont theory, which explains how organelles such as mitochondria and chloroplasts may have entered an ancestral cell. Other ideas include the nucleus-first hypothesis, the mitochondria-first hypothesis, and the eukaryote-first hypothesis. The nucleus-first hypothesis says an ancestral prokaryote first formed a membrane around its DNA, creating the...

animal and plant cell structure

Plant vs Animal Cell Division and Specialization

Plant and animal cells differ in how they divide, organize into tissues, and specialize for different jobs. Both cell types divide by mitosis in non-gametic cells and by meiosis in gametic cells, but the details are not the same. These differences help explain how each cell type supports growth and reproduction. During cell division, animal cells use centrosomes to organize spindle fibers and separate chromosomes. Plant cells do not have centrosomes. Instead, they use a microtubule-organizing...

cytoplasm

Cytoplasm and the Cell’s Internal Support

The cytoplasm is the cell’s internal space that holds organelles and the cytoskeleton. It is suspended in the cytosol, an aqueous fluid made of water, ions, salts, and many organic molecules. This fluid helps keep the cell organized and supports many cellular activities. The cytoplasm is also where protein synthesis and protein folding take place. The watery cytosol helps proteins fold correctly. In a folded protein, hydrophobic amino acid side chains tend to stay buried in the core, while...

the nucleus

Nuclear DNA, Chromatin, and Nucleoli

The nucleus is a membrane-bound organelle that stores chromosomal DNA and helps control what proteins a eukaryotic cell makes. It acts as the cell’s control center. DNA in mitochondria and chloroplasts is different because it mainly supports functions specific to those organelles. Inside the nucleus, DNA is wrapped around proteins called histones. This DNA-protein complex is called chromatin. During interphase, when the cell is not dividing, chromatin stays loosely arranged so the DNA is easy...

the dna helix

How DNA Structure Was Discovered

DNA is the genetic material that passes traits from one generation to the next in organisms and most viruses. It is made of two strands of nucleotides that twist into a spring-like double helix. The shape is not perfectly even. It also has repeating grooves called the major groove and the minor groove. The major groove forms where the sugar-phosphate backbones are farther apart. This wider space gives DNA-binding proteins, including transcription factors, better access to the bases. The minor...

the central dogma

DNA to Protein: RNA’s Role

DNA to protein flow depends on RNA as the link between genetic information and the amino acids that build proteins. Early scientists knew that DNA stores the information for cell functions and that proteins carry out most of those functions. For a long time, they did not know how the code in DNA became a working protein. At first, many people thought one gene was changed directly into its protein. Two findings in eukaryotic cells challenged that idea. Protein production does not happen in the...

mutations

Mutations in DNA and Inherited Disease

Mutations are changes in the DNA sequence. They can happen on their own during DNA copying, or they can be caused by environmental factors. Scientists describe mutations in several ways, including whether they change the amino acid sequence of a protein, how much DNA they affect, and whether they occur in somatic cells or germline cells. Some mutations are point mutations. A point mutation changes a single nucleotide in DNA. Other mutations are chromosomal alterations, which change the number...

genome size and the evolution of new genes

Genome size and gene evolution are linked through changes in DNA sequence and genome structure. Some genes can arise from parts of the genome that were not coding before, while others come from changes to existing genes. These shifts help explain how new genetic material can appear over time. A genome is the full set of DNA in an organism. Its size can change as DNA is added, removed, or rearranged. The transcript highlights that genome size is not fixed, and that these changes can shape the...

gene families

Shared Origins of Gene Families

Gene families are groups of related genes that share a common origin. They form when genes are copied and then change over time. These related genes can be found within the same genome. The video also connects gene families to homologous genes and orthologous genes. Homologous genes are genes with a shared evolutionary origin. Orthologous genes are homologous genes found in different species. Gene families help show how these relationships are used to study evolution and related gene functions.

gene evolution - fast or slow?

Gene Evolution Rates and Selection

Gene evolution can happen at different rates, and natural selection helps shape those changes. Some genes change slowly because important DNA changes are removed over time. Other genes can change more quickly when different mutations are kept in a population. The rate of evolution depends on how a gene is used and how strongly it is affected by selection. Genes with essential jobs often stay more similar across species. Genes under weaker pressure may show more variation and may evolve faster.<br...

types of genetic transfer between organisms

types-of-genetic-transfer-between-organisms

Vertical and Horizontal Gene Transfer

Genetic transfer between organisms happens in two main ways: vertical gene transfer and horizontal gene transfer. These two routes explain how hereditary material moves from one generation to the next or between organisms that are not parent and offspring. Vertical gene transfer passes genes from parent to offspring during reproduction. This is the usual way genetic information is inherited in living things. Horizontal gene transfer moves genetic material between organisms outside of...

key terms and concepts

Explore how genome size changes can shape gene evolution, including gene duplication, DNA rearrangement, and the rise of new genetic functions.

Genome Size and Gene Evolution | JoVE K12

cell biology

JoVE Core Cell Biology illustrates complex cellular processes in easy-to-understand yet comprehensive animated video lessons. This collection focuses on the essential components and functions of cells, including organelles and membranes, cellular transport, and cell energetics. It is complemented by scientist-in-action videos that demonstrate the application of cell biology in real-world research experiments.

Pennsylvania State Academic Standards

Life Science

Inheritance and Variation of Traits

3.1.9-12.P

3.1.9-12.Q

Louisiana Student Standards for Science

High School

Life Sciences

Biological Evolution: Unity And Diversity

HS-LS4-1

ohios-learning-standards-and-model-curriculum

Ohio’s Learning Standards and Model Curriculum

Heredity

Mutations

Virginia  Standards of Learning

HIgh School

BIO.5

BIO.5.b

Arizona Science Standards

HS.L3

HS.L3U1.25

HS+B.L3

HS+B.L3U1.12

Next Generation Science Standards

Heredity: Inheritance and Variation of Traits

HS-LS3-2

new-york-state-science-learning-standards

New York State Science Learning Standards

HS-LS3-1.

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

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.

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 ...

Pedigree Analysis

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

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.

LS.Bio.7.1

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 ...

Nature and Nurture

Many human characteristics, like height, are shaped by both nature&mdash;in other words, by our genes&mdash;and by nurture, or our environment. For ...

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

PCR: The Polymerase Chain Reaction

The polymerase chain reaction, or PCR, is a technique used to amplify DNA through thermocycling &#8211; cyles of temperature changes at fixed time ...

DNA Gel Electrophoresis

DNA gel electrophoresis is a technique used for the detection and separation of DNA molecules. An electric field is applied to a gel matrix comprised of ...

DNA Isolation

DNA isolation protocols can be fast and straightforward or complex and time-consuming depending on the type and quality of DNA required for further ...

Restriction Enzymes

Restriction enzymes are bacterial enzymes used to cut DNA in a sequence-specific manner. To cleave DNA, they bind to specific palindromic sequences called ...

Analyze and interpret data to compare DNA samples.

LS.Bio.8.1

Understand genetic mechanisms for variation.

Genome Size and Gene Evolution

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