Name: genomic imprinting in human disease
Uploaded: 2020-11-23T11:47:38.000Z
Duration: 2 min 30 s
Channel: JoVE

البصمة الوراثية هى ظاهرة حيث تنظيم التعبير الجيني يكون متأثر بالوالدين الذين مرروا الجين لذريتهم. الخلايا الجسدية للعديد من الكائنات الحية،مثل الثدييات،تكون ثنائية المجموعة الكروموسومية. وهذا يعني, أن كل منهما لديه نسختان من الجينوم واحدة وُرّثت من الأب وواحدة من الأم.

النُسخ من نفس الجين في الخلايا الجسدية تُعرف باسم الأليلالات. في معظم الحالات،كلا الأليلان يتم التعبير عنهما في وقت واحد. ومع ذلك،عدد قليل من الجينات يتم التعبير عنهم بناءًعلى مصدر الوراثة بسبب بصمة أو علامة مصاحبة للجين،مثل إضافة مجموعة ميثايل هذه الميثلة تكون مقاومة لعملية نزع مجموعة الميثايل التى تحدث بعد الإخصاب وبالتالي،يتم توريثها للأبناء.

مثيلة دى إن إيه ممكن أن تنظم التعبير الجينى إيجاباًأو سلباًفي الفئران،نسخة من جين عامل النمو الشبيه بالأنسولين-2 الموروث من الأم تكون صامته. بينما النسخة من الأب يتم التعبير عنها بسبب التبصُم. تسلسلات التنظيمية تثبط جين عندما يرتبط البروتين العازل.

بالنسبة للأليل الموروث من الأم،غياب الميثلة تؤدى إلى إلى قمع الجين بواسطة بروتين العزل. وبالنسبة للأليل من الأب،الميثلة في هذا التسلسل يؤثر بشكل إيجابي على تعبير الأليل عن طريق منع البروتين من الإرتباط،مما يؤدي إلى التعبير الجيني. يمكن أن تكون البصمة الوراثية ضارة للذرية عندما يكون الأليل الذي تم التعبير عنه متحور.

وعلى النقيض من أغلب الجينات،فإن الاليل الآخر لا يمكنه تعويض الطفرة بسبب الإسكات بواسطة البصمة الوراثية. على سبيل المثال،المثبط سايكلين المعتمد على الكيناز هو جين مشفر لبروتين مسؤول عن تعديل إنقسامات الخلية. البصمة الجينية تضمن تعبير الأليل من الأم فقط.

غياب او تحور الأليل من الأم يساهم في حالة معروفة بمتلازمة بكموذ ويديمان تتميز بالحجم الكبير للجسم،لسان كبير،ونتوء للأعضاء الداخلية خارج الجسم عبر سرة البطن.

<ol>
	<li>بتلر إم جي (2009). اضطرابات البصمة الجينومية لدى البشر: مراجعة مصغرة. مجلة المساعدة على الإنجاب وعلم الوراثة ، 26 (9-10) ، 477-486.</li>
	<li>لوبو ، آي (2008) البصمة الجينومية وأنماط وراثة المرض. تعليم الطبيعة 1 (1): 66</li>
</ol>

البصمة الجينومية والميراث

Genomic Imprinting and Inheritance

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ترث الكائنات ثنائية الصيغة الصبغية المادة الوراثية من خلال الكروموسومات من كلا الوالدين. تُعرف النسخ من نفس الجين باسم الأليلات. في معظم الحالات، يتم التعبير عن كلا الأليلين في وقت واحد، مما يسمح للعمليات الخلوية المختلفة بالعمل على النحو الأمثل. إذا كان أحد الأليلات مفقودًا أو متحورًا، فإن التعبير عن الأليل الآخر يمكن تعويضه؛ ومع ذلك، هذا ليس صحيحا بالنسبة لجميع الجينات.

ويعتمد التعبير عن بعض الجينات على الأب الذي قام بتمرير الجين إلى الأبناء، من خلال ظاهرة تعرف باسم البصمة الجينية. في البصمة الجينية، يتم طباعة ترميز الحمض النووي للجين أو تسلسله التنظيمي بعلامات كيميائية مثل مجموعات الميثيلة، فقط في النسخة الموروثة من أحد الوالدين. هذه العلامة مقاومة لإزالة الميثيلة أثناء الإخصاب ويتم نقلها إلى النسل للتعبير الجيني الانتقائي.

في بعض الأحيان، يتم توريث نسختين من الجين من نفس الوالد، ويكون جين الوالد الآخر مفقودًا. يحدث التكرارالأمومي الأحادي عند وجود نسختين من جين الأم؛ في المقابل، يحدث التكرارالأبوي الأحادي عندما يتم وراثة نسختين من الأب. إذا كان هناك نسختان من الأليل الصامت وإذا كان الأليل المعبر عنه عادة غائبا، فغالبا ما يؤدي ذلك إلى اضطراب وراثي.

الأمراض البشرية المرتبطة بالبصمة الجينية

تشمل الأمراض التي تصيب البشر المرتبطة بالبصمة الجينية متلازمة بيكويث-فيدمان، ومتلازمة أنجلمان، ومتلازمة برادر-ويلي، وبعض أنواع السرطان.

ترتبط كل من متلازمة برادر ويلي ومتلازمة أنجلمان بالكروموسوم 15. وتحدث متلازمة برادر ويلي عندما يكون هناك خلل أحادي الوالدين لدى الأم. يمكن للأشخاص الذين يعانون من هذه المتلازمة أن يظهروا السمنة وتأخر النمو الجنسي والإعاقات العقلية. ترتبط متلازمة أنجلمان بالاضطراب الأبوي الأحادي. قد يظهر على الأشخاص المصابين بهذه المتلازمة إعاقات عقلية وقصور في النمو واضطرابات في النوم وفرط النشاط.
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ترث الكائنات ثنائية الصبغيات المادة الوراثية من خلال الكروموسومات من كلا الوالدين. تعرف نسخ من نفس الجين باسم الأليلات. في معظم الحالات ، كلاهما ...

Education

JoVE Core

Molecular Biology

البيولوجيا الجزيئية

Unit 1

الوحدة الأولى

Gene Expression

التعبير الجيني

KEY TERMS AND CONCEPTS

المصطلحات والمفاهيم الأساسية

genomic imprinting in human disease

Genomic imprinting affects how some inherited genes are turned on or off in human cells. Diploid organisms inherit chromosomes from both parents, and each gene usually has two alleles. In most cases, both alleles are expressed. If one allele is missing or mutated, the other can often compensate, but some genes do not work that way.

In genomic imprinting, a gene or its regulatory sequence carries chemical tags, such as methyl groups, on the copy inherited from only one parent. These tags are resistant to demethylation during fertilization. That means the imprint can survive into the offspring and help control which allele is expressed.

Problems can occur when both copies of a gene come from the same parent. Maternal uniparental disomy means two maternal copies are present, while paternal uniparental disomy means two paternal copies are present. If the active allele is missing and the silenced allele is inherited twice, a genetic disorder may result.

Human diseases linked to genomic imprinting include Beckwith-Wiedemann syndrome, Angelman syndrome, Prader-Willi syndrome, and some cancers. Prader-Willi syndrome is associated with maternal uniparental disomy of chromosome 15. It can cause obesity, sexual under-development, and mental disabilities. Angelman syndrome is linked to paternal uniparental disomy of chromosome 15. It may cause mental disabilities, developmental deficiencies, sleep disorders, and hyperactivity.

Genomic Imprinting in Human Disease

cell specific gene expression

How Cells Switch Genes On and Off

Cells switch genes on and off to make different proteins for different jobs. In multicellular organisms, many cell types are built from the same DNA, but they do not use the same genes in the same way. This difference in gene expression helps explain why cells can look and act so differently. Liver cells are a clear example. They help detoxify blood, make bile to help digest fats, and produce proteins needed for metabolism. To do these jobs, liver cells must express a specific set of genes.

regulation of expression occurs at multiple steps

regulation-of-expression-occurs-at-multiple-steps

How Cells Control Gene Expression

Cells control gene expression at several points between DNA and protein. The most common control point is transcription. At this stage, proteins bind to short regulatory DNA sequences and can either increase or reduce transcription of the linked gene. After transcription, a precursor mRNA is made. This pre-mRNA contains exons, which code for protein, and introns, which do not. It must be processed before translation, and splicing removes the introns and joins the exons. Cells can also regulate...

cis-regulatory sequences

How Cis-Regulatory DNA Controls Transcription

Cis-regulatory sequences are short, non-coding DNA segments that control gene transcription. They sit on the same chromosome as the genes they regulate and act as binding sites for transcriptional regulators. In eukaryotes, these proteins help control gene expression patterns in different cell types. These DNA sequences can be close to a gene or thousands of bases away. When they are far from the gene in the DNA sequence, they are often brought close together in space because chromosomes are...

cooperative binding of transcription regulators

cooperative-binding-of-transcription-regulators

How Transcription Factors Bind DNA

Transcriptional regulators bind to cis-regulatory DNA sequences to control gene transcription. These DNA sequences are very short, usually fewer than ten nucleotide pairs long. Because they are so short, the same sequence can appear by chance in many places across the genome. Some regulators can also bind to groups of similar sequences. That raises the chance of random binding even more. To lower this risk, transcription regulators often form dimers, which are pairs of proteins that bind a DNA...

prokaryotic transcriptional activators and repressors

prokaryotic-transcriptional-activators-and-repressors

Operon Control by Activators and Repressors

Operon control in prokaryotes depends on activators and repressors. Prokaryotic genes are often arranged in groups, not one by one like in eukaryotes. Genes that help carry out the same biochemical process are placed together with their regulatory elements. This group is called an operon, and it is transcribed into a single polycistronic mRNA strand. Activators and repressors are DNA-binding proteins that control transcription in an operon. Activators bind near the promoter, which is the site...

operons

Operons in Bacterial Gene Control

Operons help bacteria control groups of genes at the same time. An operon is a set of genes that are regulated together and can be turned on or off as a unit. This shared control helps bacteria respond quickly to changes in their environment. In many operons, a promoter gives RNA polymerase a place to bind and start transcription. The operon also includes a regulatory region that helps control whether the genes are expressed. When conditions change, the cell can use this setup to manage gene...

the eukaryotic promoter region

Eukaryotic Promoter Motifs and Gene Control

The eukaryotic promoter region is a stretch of DNA located upstream of a gene. It includes an RNA polymerase binding site, a transcription start site, and several cis-regulatory sequences. These DNA signals help control when transcription begins. The promoter can be divided into proximal and distal regions. The proximal promoter lies close to the gene and includes cis-regulatory sequences and the core promoter. The core promoter is the RNA polymerase binding site, and it is usually found...

co-activators and co-repressors

Chromatin Control in Gene Transcription

Chromatin control plays a major role in gene transcription in eukaryotes. Gene expression is regulated by several proteins that work together at a gene regulatory site. Some of these proteins bind directly to specific DNA sequences, while co-regulators attach to those regulators but do not bind DNA on their own. Co-regulators can act as co-activators or co-repressors, depending on the complex they join. One co-regulator may even switch roles in different settings. For example, the...

eukaryotic transcription activators

How Transcription Activators Turn Genes On

Transcription activators are proteins that help turn genes on by promoting transcription from DNA to RNA. They often have two parts. One part binds to DNA, and the other part activates transcription. In some proteins, such as the glucocorticoid receptor and MyoD, one domain can do both jobs. The DNA-binding part recognizes specific regulatory sequences on the DNA. These binding domains are grouped into families based on their structure. Common examples include the leucine zipper, zinc finger,...

eukaryotic transcription inhibitors

How Eukaryotic Gene Repressors Work

Eukaryotic gene repressors help turn specific genes off when the cell needs to control growth, development, or other biochemical processes. These DNA-binding proteins regulate gene expression in eukaryotes. Their presence at the right time and place can be triggered by hormones and signals from other cells. Most transcription inhibitors have two main parts. One part binds DNA, and the other is a repressor domain, which helps shut down transcription. Repressor domains can connect with basal...

combinatorial gene control

Gene Expression by Transcription Factor Combinations

Gene expression can depend on combinations of transcription factors working together. In combinatorial gene control, several transcription factors act in a coordinated way to regulate a single gene. If one or more of these factors are missing, the level of gene expression or repression can change a lot. This kind of control helps explain how a relatively small number of transcription factors can regulate a very large number of genes. More than 30,000 genes are controlled by about 2,000 to...

induced pluripotent stem cells

Reprogramming Cells into Stem Cells

Induced pluripotent stem cells are created by reprogramming mature cells back into a stem-cell state. This process shows that specialized cells can be changed into cells with broader developmental potential. The topic is important in biology because it links cell identity, gene control, and stem cell research. These cells begin as ordinary body cells and are pushed to de-differentiate, or lose their specialized features. After reprogramming, they behave like pluripotent stem cells, which means...

master transcription regulators

MEF2C and Gene Control Cascades

MEF2C is a master transcription regulator that controls gene expression in coordinated cascades. These regulators are proteins that manage the activity of multiple genes that often work together to produce a complex outcome. When a master transcription regulator is activated, it can start a chain of transcriptional activation that supports that outcome. Master transcription regulators can act in two main ways. They may bind directly to the regulatory sequences of several genes involved in a...

epigenetic regulation

DNA Methylation and Histone Changes

Epigenetic regulation controls gene activity without changing the DNA sequence. It helps determine when genes are turned on or off in a cell. Two major epigenetic mechanisms are DNA methylation and histone modification. DNA methylation adds chemical groups to DNA, while histone changes affect how tightly DNA is packed around histone proteins. These changes can make genes easier or harder to use. In high school biology, epigenetic regulation is important for understanding how cells with the...

genomic imprinting and inheritance

Genomic imprinting affects how some inherited genes are turned on or off in human cells. Diploid organisms inherit chromosomes from both parents, and each gene usually has two alleles. In most cases, both alleles are expressed. If one allele is missing or mutated, the other can often compensate, but some genes do not work that way. In genomic imprinting, a gene or its regulatory sequence carries chemical tags, such as methyl groups, on the copy inherited from only one parent. These tags are...

key terms and concepts

Learn how genomic imprinting controls gene expression and why maternal or paternal uniparental disomy can lead to disorders such as Prader-Willi and Angelman syndromes.

Genomic Imprinting in Human Disease | JoVE K12

molecular biology

JoVE Core Molecular Biology showcases the molecular processes of the cell through clear and concise animated video lessons. Additionally, in scientist-in-action videos, these concepts' application is demonstrated through real experiments in modern laboratories.

Genomic Imprinting in Human Disease

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