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(单词翻译:双击或拖选)
...lead to the end of diseases like cancer...
Alzheimer's, Parkinson's, diabetes1.
The list is endless.
We were thinking of genes2 in a very mechanical way. We were thinking of them just in terms of the sequence of the letters when we were working out how we could work out what all the letters were in the book.
Scientists estimated that the human genome, the book of life, would contain around 100,000 genes.
And then when they started sequencing they, they realized there may be 100,000 genes, and it popped down to 60, and then it popped down to 50, I mean, and slowly went down to a much smaller number. In fact we found out that the human genome is probably not as complex and doesn't have as many genes as, as plants do. So that they made us really question it all. If the genome has less genes in this species versus3 this species, and we are more complex potentially, what's going on here?
Now, scientists estimate there are probably less than 30,000 genes.
We believed, I believed naively4 that we would be able to find the genetic5 components6 of common diseases. That's proven to be very difficult. The idea of one-gene-one-disease does not explain it all.
30,000 genes didn't appear enough to explain human complexity7. There had to be something they'd missed. The first hints of what was missing lay in the curious paradox8 of the Prader-Willi and Angelman syndromes10, two quite different diseases caused by exactly the same genetic fault. When Pembrey looked at the inheritance pattern for their conditions he noticed something even stranger.
What really mattered was the origin of the Chromosome11 15 that had the deletion. If the deletion was on the Chromosome 15 that the child had inherited from father then you had Prader-Willi syndrome9. Whereas, if the, er, deletion, er, was inherited from the mother, er, you had the Angelman syndrome.
It was a complete surprise that the same missing strip of DNA12 could cause one disease when it came from the mother and a completely different disease when it came from the father. It was as if the genes knew where they came from.
You've got a developing fetus13 manifesting this condition. How does the Chromosome 15 know where it came from? It, there must have been a tag or an imprint14 placed on that chromosome during either egg or sperm15 formation in the previous generation to, to say "Hi, I came from mother, I came from father" and we are functioning differently. So that's the key thing that although the DNA sequence is the same the different sets of genes were being silenced depending on whether it came from the mother or from the father.
New Words & Phrases:
Alzheimer's: Alzheimer's disease is a condition in which a person's brain gradually stops working properly. 【医】阿耳茨海默氏病,早老性痴呆病
Parkinson's: 【医】帕金森氏病
fetus : (= foetus)A fetus is an animal or human being in its later stages of development before it is born. 胎;(三个月后的)胎儿
1 diabetes | |
n.糖尿病 | |
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2 genes | |
n.基因( gene的名词复数 ) | |
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3 versus | |
prep.以…为对手,对;与…相比之下 | |
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4 naively | |
adv. 天真地 | |
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5 genetic | |
adj.遗传的,遗传学的 | |
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6 components | |
(机器、设备等的)构成要素,零件,成分; 成分( component的名词复数 ); [物理化学]组分; [数学]分量; (混合物的)组成部分 | |
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7 complexity | |
n.复杂(性),复杂的事物 | |
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8 paradox | |
n.似乎矛盾却正确的说法;自相矛盾的人(物) | |
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9 syndrome | |
n.综合病症;并存特性 | |
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10 syndromes | |
n.综合征( syndrome的名词复数 );(某种条件下有共同特征的)一系列表现(事件、举动等) | |
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11 chromosome | |
n.染色体 | |
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12 DNA | |
(缩)deoxyribonucleic acid 脱氧核糖核酸 | |
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13 fetus | |
n.胎,胎儿 | |
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14 imprint | |
n.印痕,痕迹;深刻的印象;vt.压印,牢记 | |
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15 sperm | |
n.精子,精液 | |
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