Recombinant DNA technology allows scientists to cut segments of DNA from one type of organism and combine them with the genes of a second organism. Also called genetic engineering. Recombinant DNA technology is a method by which relatively simple organisms, such as bacteria or yeast, or even mammalian cells in culture, can be induced to make quantities of human proteins, including interferons or grow tobacco plants that produce monoclonal antibodies, and goats that secrete a clot-dissolving heart attack drug, tissue plasminogen activator (TPA), in their milk.
Another facet of recombinant DNA technology involves gene therapy. The goal of this therapy is to replace defective genes, or to endow a cell with new capabilities. In 1989, the feasibility and safety of gene transfer was demonstrated when tumor-infiltrating lymphocytes (TILS) were extracted from a patient, equipped with a marker gene (so they could be tracked and monitored), and then re-injected into patients with advanced cancer. To deliver the gene into the TILS, the scientists used a virus, exploiting its natural tendency to invade cells, before being used as a vector, the virus was altered so that it could not reproduce or cause disease. This experiment demonstrated that gene-modified cells could survive for long periods in the bloodstream and in tumor deposits without harm to the patient.
The earliest attempts to use genes therapeutically focused on a form of severe combined immunodeficiency disease (SCID), which is caused by the lack of an enzyme due to a single abnormal gene. The gene for this enzyme-adenosine deaminase (ADA)—is delivered into the patient's T cells by a modified retrovirus. When the virus splices its genes into those of the T cells, it simultaneously introduces the gene for the missing enzyme. After the treated T cells begin to produce the missing enzyme, they are injected back into the patient.
Gene therapy is now being used with some cancer patients. TILS reinforced with a gene for the antitumor cytokine known as tumor necrosis factor (TNF) have been administered to patients with advanced melanoma, a deadly form of skin cancer. Plans are under way to engineer a cancer “vaccine” designed to improve anticancer immune responses by taking small bits of tumor from patients with cancer, outfitting the tumor cells with genes for immune cell activating cytokines such as LL2, and re-injecting these gene-modified tumors into the patient. While the thought of reintroducing a cancerous tumor into a patient seems somewhat frightening, the enhanced immune response triggered by this technique may help prevent the recurrence of cancer.
1.What innate characteristic of viruses did researchers take advantage of in order to transport genes into TILS?
2.According to the passage, SCID is caused by( ).
3.Why might cancer patients be leery of the prospect of a cancer “vaccine” as discussed in this passage?
4.Adenosine deaminase (ADA) is transferred into the T cells of a patient via which of the following?
问题1选项
A.Protective protein coat
B.Affinity for invading cells
C.Non-cellular consistency
D.Ability to produce DNA from RNA
问题2选项
A.an overabundance of monoclonal antibodies
B.an overabundance of tumor necrosis factor
C.a lack of tumor necrosis factor
D.a lack of adenosine deaminase
问题3选项
A.Vaccine recipients will be re-injected with cancerous material.
B.The vaccine is derived from the tobacco plant.
C.The safety of genetic transfer has not yet been proven.
D.Genetic material from the vector could invade the vaccine recipient’s bloodstream.
问题4选项
A.Marker gene
B.TILS
C.Interferon
D.Modified retrovirus
第1题:
【选项释义】
What innate characteristic of viruses did researchers take advantage of in order to transport genes into TILS? 研究人员利用了病毒的什么先天特征来将基因运输到肿瘤浸润淋巴细胞(TILS)中?
A. Protective protein coat. A. 保护性蛋白外壳。
B. Affinity for invading cells. B. 入侵细胞的倾向。
C. Non-cellular consistency. C. 非细胞的一致性。
D. Ability to produce DNA from RNA. D. 从核糖核酸(RNA)中产生脱氧核糖核酸(DNA)的能力。
【考查点】细节事实题。
【解题思路】根据题干中信息词transport genes into TILS定位到第二段第四句,该处讲到“为了将这种基因导入肿瘤浸润淋巴细胞(TILS),科学家们使用了一种病毒,利用其入侵细胞的自然倾向。”,可知科学家利用了病毒入侵细胞的倾向这个先天特征,因此B选项正确。
【干扰项排除】
A选项“保护性蛋白外套”,C选项“非细胞的一致性”和D选项“从核糖核酸(RNA)中产生脱氧核糖核酸(DNA)的能力”:文中没有提到,属于无中生有。
第2题:
【选项释义】
According to the passage, SCID is caused by __________. 根据文章,严重联合免疫缺陷(SCID)是由__________引起的。
A. an overabundance of monoclonal antibodies A. 单克隆抗体过多
B. an overabundance of tumor necrosis factor B. 肿瘤坏死因子过多
C. a lack of tumor necrosis factor C. 缺乏肿瘤坏死因子
D. a lack of adenosine deaminase D. 缺乏腺苷脱氨酶
【考查点】细节事实题。
【解题思路】根据题干中信息词SCID is caused定位到第三段第一、二句,该处讲到“严重联合免疫缺陷病(SCID),由单个异常基因引起的酶缺乏引起(caused by the lack of an enzyme)。这种酶的基因——腺苷脱氨酶(ADA)——通过一种改良的逆转录病毒进入患者的T细胞。”,可知SCID是由于缺乏ADA引起的。因此D选项正确。
【干扰项排除】
A选项“单克隆抗体过多”,B选项“肿瘤坏死因子过多”和C选项“缺乏肿瘤坏死因子”不是正确答案,属于曲解原文。
第3题:
【选项释义】
Why might cancer patients be leery of the prospect of a cancer “vaccine” as discussed in this passage? 为什么癌症患者可能对这篇文章中讨论的癌症“疫苗”的前景持怀疑态度?
A. Vaccine recipients will be re-injected with cancerous material. A. 接受疫苗的人将被重新注射癌症物质。
B. The vaccine is derived from the tobacco plant. B. 疫苗是从烟草植物中提取的。
C. The safety of genetic transfer has not yet been proven. C. 基因转移的安全性尚未得到证实。
D. Genetic material from the vector could invade the vaccine recipient’s bloodstream. D. 载体中的遗传物质可以侵入疫苗接受者的血液。
【考查点】推理判断题。
【解题思路】此题定位到文章最后一句,该处讲到“将癌症肿瘤重新植入患者体内(reintroducing a cancerous tumor into a patient)的想法似乎有些可怕(frightening)。”,可知癌症患者可能因为疫苗是把癌症物质重新注入体内而对此怀疑。因此A选项正确。
【干扰项排除】
B选项“疫苗是从烟草植物中提取的”和D选项“载体中的遗传物质可以侵入疫苗接受者的血液”:文章没有提到,属于无中生有;
C选项“基因转移的安全性尚未得到证实”:对应第二段第三句“证明了基因转移的可行性和安全性(the feasibility and safety of gene transfer was demonstrated)。”,可知本选项和文章内容不符,属于反向干扰。
第4题:
【选项释义】
Adenosine deaminase (ADA) is transferred into the T cells of a patient via which of the following? 腺苷脱氨酶(ADA)通过下列哪一种途径转移到病人的T细胞中?
A. Marker gene. A. 标记基因。
B. TILS. B. 肿瘤浸润淋巴细胞。
C. Interferon. C. 干扰素。
D. Modified retrovirus. D. 修饰逆转录病毒。
【考查点】事实细节题。
【解题思路】根据题干中信息词(ADA) is transferred into the T cells定位到第三段第二句,该处讲到“这种酶的基因——腺苷脱氨酶(ADA)——通过一种改良的逆转录病毒(by a modified retrovirus)进入患者的T细胞。”,可知ADA是通过修饰逆转录病毒的途径转移到病人的T细胞中,因此D选项正确。
【干扰项排除】
A选项“标记基因”,B选项“肿瘤浸润淋巴细胞”和C选项“干扰素”不是正确答案,属于曲解原文。