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Ohno 1970 年的开创性工作普及了基因复制和分化的概念。 DNA序列比较研究表明,细菌、古细菌和真核生物中的很大一部分基因是通过基因复制和分化产生的,表明其在进化中的关键作用。
该基因的复制拷贝称为旁系同源基因。 具有相似序列和功能的旁系同源物形成一个基因家族。 在几个物种中,有大量基因家族的…
基因重复是指编码基因的DNA区域发生复制,在同一基因组内产生额外拷贝的过程。这些基因的重复拷贝——称为旁系同源基因(paralogs),之后可能发生突变,并以以下某种方式产生分歧。
首先是假基因的形成。在此过程中,一个基因旁系同源物可能获得有害突变,从而转变为一种无功能的拷贝,称为假基因。
第二种是亚功能化,即两个旁系同源基因在不同的蛋白质编码区或外显子中分别获得突变,从而将原始基因的功能分配给两者。然而,这两个旁系同源基因的蛋白质产物相互补充,共同表现出原始基因的功能。
例如,在原始鱼类和海洋动物中,单链珠蛋白作为血液中携带氧气的分子。
在进化过程中,珠蛋白基因发生复制并进一步亚功能化,形成两个略有不同的基因,分别编码α-珠蛋白和β-珠蛋白,这两种蛋白结合形成血红蛋白分子,该分子由四个亚基组成,存在于现今大多数脊椎动物中。
第三种是新功能化(Neo-functionalization)。在此过程中,一个旁系同源基因获得新的有利突变,可能导致新基因的进化;而另一个旁系同源基因则保留原始功能。
例如,人类β-珠蛋白基因发生复制并积累突变,从而产生了一种称为胎儿β-珠蛋白的新基因,该基因仅在人类胎儿中表达。然而,在出生后不久,β-珠蛋白基因便重新接管β-珠蛋白的合成。
人类三色视觉的演化是新功能化(neofunctionalization)的另一个有趣例子。在现代猿类出现之前,早期灵长类动物由于存在视蛋白蓝光和绿光基因,仅具有二色视觉。
随后,绿色视蛋白基因发生复制,并新功能化为一种新的红色视蛋白基因。
因此,在基因重复事件之后进化的物种,例如旧世界猴、猿类和人类,具有三个视蛋白基因,赋予其三色视觉能力。
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Q1: What is gene duplication and how does it occur in genomes?
Gene duplication is a process where a DNA region coding for a gene duplicates, creating additional copies within the same genome. Duplication can arise through unequal crossing over during meiosis, replication slippage where DNA polymerase dissociates and realigns incorrectly, or retrotransposition where mRNA is reverse transcribed into DNA copies called retrogenes that reinsert into the genome.
Q2: What are paralogs and how do they relate to gene families?
Paralogs are duplicated copies of genes with similar sequences and functions. When paralogs share enough similarity, they form a gene family. Gene families are widespread across species; for example, the trypsin gene family in D. melanogaster has over 111 members, while the olfactory receptor gene family in mammals contains around 1000 member genes.
Q3: How does sub-functionalization differ from neo-functionalization after gene duplication?
Sub-functionalization occurs when both paralogs acquire mutations in different protein domains, partitioning the original gene function between them while their protein products complement each other. Neo-functionalization happens when one paralog acquires novel mutations leading to a new gene function, while the other retains the original function, as seen with fetal β-globin evolution.
Q4: What is a pseudogene and how does it form from gene duplication?
A pseudogene is a nonfunctional copy of a gene that forms when one paralog acquires deleterious mutations after duplication. Pseudogenes commonly arise from retrotransposition, where inserted retrogenes lack promoters and regulatory elements necessary for transcription, causing them to lose function over time.
Q5: How did hemoglobin evolution demonstrate sub-functionalization in vertebrates?
In primitive fish and marine animals, a single globin gene encoded oxygen-carrying proteins. During evolution, the globin gene duplicated and sub-functionalized into α-globin and β-globin genes. These proteins associate to form hemoglobin with four subunits found in modern vertebrates, with each protein complementing the other to maintain oxygen transport function.
Q6: What role did gene duplication play in the evolution of primate color vision?
Early primates had dichromatic vision from Blue and Green opsin genes. The Green opsin gene later duplicated and neo-functionalized into a novel Red opsin gene. Species evolving after this duplication, including old world monkeys, apes, and humans, gained three opsin genes enabling tricolor vision.
Q7: What is whole-genome duplication and how does it differ from single gene duplication?
Whole-genome duplication occurs when entire chromosomes or genomes duplicate, often through chromosome segregation failures during meiosis. Unlike single gene duplication, this creates multiple copies of all genes simultaneously. For example, wheat genomes have duplicated six times, creating a hexaploid organism with multiple chromosome sets.