Genetic mutation | gene mutation

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Genetic mutation in humans explained. This lecture explains about gene mutation and chromosomal mutation in animals. gene mutations and genetic mutations are dangerous and the effect is horrifying.
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A gene mutation is a permanent alteration in the DNA sequence that makes up a gene, such that the sequence differs from what is found in most humans. Mutations variety in dimension; they are able to have an impact on wherever from a single DNA building block (base pair) to a huge segment of a chromosome that involves more than one genes.
Gene mutations can be classified in two most important approaches:
Hereditary mutations are inherited from a mother or father and are present for the period of a individual’s lifestyles in practically each mobile within the body. These mutations are also referred to as germline mutations due to the fact they're present within the mum or dad’s egg or sperm cells, which might be also called germ cells. When an egg and a sperm mobilephone unite, the resulting fertilized egg telephone receives DNA from both mum and dad. If this DNA has a mutation, the youngster that grows from the fertilized egg may have the mutation in every of his or her cells.
Acquired (or somatic) mutations arise at some time during a character’s lifestyles and are present handiest in specified cells, not in each telephone within the physique. These changes can also be induced by using environmental explanations corresponding to ultraviolet radiation from the solar, or can occur if a mistake is made as DNA copies itself for the period of telephone division. Acquired mutations in somatic cells (cells rather then sperm and egg cells) can't be passed on to the next iteration.
Genetic changes that are described as de novo (new) mutations can be either hereditary or somatic. In some cases, the mutation occurs in a man or woman’s egg or sperm mobile but isn't present in any of the character’s other cells. In other instances, the mutation happens in the fertilized egg quickly after the egg and sperm cells unite. (it's commonly unimaginable to tell exactly when a de novo mutation happened.) because the fertilized egg divides, each and every resulting phone within the developing embryo could have the mutation. De novo mutations could provide an explanation for genetic issues wherein an affected child has a mutation in each mobilephone in the physique however the mum and dad don't, and there is not any loved ones historical past of the sickness.
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Today I know much about MUTATION . I am 9 years old and I am in 4th class But, I love to know new things in the nature and much more . THANK YOU 😁

nimitkumar
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Thank you best teacher ever this is final year of my university and I used 95 percentage of your videos during my exams all of them was very helpful I do appreciate you I will always support you by sharing or writing comments and other ways keep going for our next generation!!!

ruhidyusifov
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hi shomu. I have a question about the point additions that cause frame shifts. so when you added that A to the sequence, does the complementary DNA strand also get an addition (i.e. an additional T)? or is it just the one strand that gets mutated? thanks!

iluvbeef
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No one could explain this complicated biological observations than you. Salute

ashrafhossain
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Help me what is one copy of a double mutation mean, I need help understanding

lucious
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Surely Allah will bless u !! And serve u with beautiful life..

dipeshmehta
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I've been writing notes for this topic for 3 hours and I didn't understand it.. and I just watched your videos and I understood it.
Thank you !!!

abdullah
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Sir,
Why mutation is helpful in secondary metabolite so plz tell me the reason

paditpadit
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Can you please tell me how does the ph effect on mutations.

pandapanda
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It will b very helpful if u will make a video about mutation affecting the regulation of gene expression.vry much need of this vdo

sohinidutta
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I have one question since 12th: Why insertion or deletion of multiple of 3 bp is not a frame shift mutation? Insertion may be any where, I may be b/w two codons or b/w bp of one codon.

naitikchauhan
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Hi everyone ! I know this may be sort of off topic but I am a 27 yo female and I have Essential Thrombocythemia with the “SF1” gene mutation/myeloid malignancy (48.5% proliferation). Is there anyone here that is familiar with SF1 and can possibly explain ? I am finding very little information on the mutation. I was diagnosed with a platelet count of 1.4 million and I am intolerant of oral platelet reducing drugs and interferon has negatively affected my thyroid function. I am seeking some answers. If any of you may have some insight, please feel free to respond ! ✊🏽

lissadipity
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Is dna is most susceptible to uv radiation?

whatwhyhowmedia
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can you please explain the cause of mutation or precisely mechanism of mutation? Thank you in advance...

terizla
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Sir one question ...why microbial mutation is necessary for formentation process

rahamatkhan
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Sir pranam... I Have a question that what is the difference between Gene mutation&chromosomal mutation?

monalishapriyadarshini
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is there any video regarding crossing over in detail?

resnank
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Sir I understood all but I dont know what is amplification

bhalagukan
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Can there be any mutation without foreign agent or factor?

Christopher_Mang
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Thank you for the information. You are true. No need to see other videos if you see this video. You can learn all about the genetic mutation from this video.

aws_all