单选题 That smoking causes lung cancer is well established. But what causes smoking? This is the question at the heart of a study published in Nature by a group of researchers who work at deCODE, an Icelandic genomics company. They do not, quite, answer it. But they do think they have the answer to the related question of why some smokers smoke in moderation whereas others are rarely found without a fag in their hands—and thus why some people are, genetically speaking, more susceptible to lung cancer than others.
That answer lies in part of human chromosome 15, and depends on what is known as allele T of SNP rs1051730. A SNP, or single-nucleotide polymorphism, to give its full name (the short version is pronounced "snip"), is a place where genomes routinely differ from one another by a single genetic letter.
In this case, the variation happens inside a gene for one of the receptor molecules that nicotine attaches itself to when it produces its buzz. Based on a study of 13,945 Icelandic smokers, deCODE"s researchers showed that having a T in the appropriate part of the gene correlates very strongly indeed with being a heavy smoker. The team estimates that the chance of their being wrong is less than one in a thousand trillion.
Not surprisingly, having the T variant also correlates with the chance of a smoker getting lung cancer. Each copy (there may be none, one or two, since one can come from a person"s father and one from his mother) increases that chance by 30%. The T variant does not, however, increase the likelihood that someone will take up smoking in the first place. That is either a matter of free will or, if it is genetic, is controlled by genes somewhere else. It all looks neat and simple—and extremely plausible. Genes promote smoking; smoking promotes cancer. However, it might be wrong, for another paper in Nature, and a third in its sister journal Nature Genetics, report similar studies that have drawn rather different conclusions.
Paul Brennan and Christopher Amos both agree that something significant is going on in the part of chromosome 15 studied by deCODE. But they have concluded that genetic variation there acts directly on a person"s susceptibility to lung cancer, rather than acting indirectly by modifying his smoking behavior. That does not mean the gene or genes in question actually cause lung cancer. Rather, it means that they amplify the effects of smoking instead of the amount of smoking.
Like deCODE, both Dr. Brennan (who works at the International Agency for Research on Cancer, in France) and Dr. Amos (who works at the University of Texas) identified rs1051730 as an important SNP. Unlike deCODE, though, both think a second SNP, rs8034191, is involved as well. That, and the fact that the region of chromosome 15 under scrutiny has two other nicotine-receptor genes in it, suggests the situation may indeed be more complex.
On top of this, Dr. Brennan and Dr. Amos both used a different method from deCODE"s. They compared lung-cancer patients directly with otherwise similar cancer-free smokers, in what is known as a case controlled study, and concluded that genetic variants in the nicotine-receptor-rich part of chromosome 15 are changing not smokers" behavior, but their susceptibility to cancer. Moreover, Dr. Brennan also claims to have discovered an increased susceptibility to lung cancer in non-smokers with the relevant SNPs, though his sample size is small and his result is not supported by Dr. Amos"s work.
These contradictory conclusions are both puzzling and intriguing. DeCODE has one further piece of evidence in its favor. Besides the correlation with lung cancer, the T variant also seemed to correlate with peripheral arterial disease, another common side-effect of smoking. On the other hand, the firm also acknowledges that the link it thinks it has discovered does not account for the whole of the risk of smoking-induced lung cancer. What is not in doubt, however, is that there is some sort of a link between genetics and lung cancer.
That raises interesting issues, particularly as genetic testing becomes easier. DeCODE has already announced it will add rs1051730 to the standard screen it offers to those who wish to know their susceptibility to diseases. The day is not far off, therefore, when those who take the essentially irrational decision to start smoking tobacco will be able to find out in advance exactly how foolish they are being.
单选题 All of the following have enough evidence EXCEPT that ______.
【正确答案】 C
【答案解析】[解析] 第4段倒数第2句提到基因诱导吸烟,而最后一句却用it might be wrong来否定这个说法,且第5段第2句提到基因变异与个人吸烟习惯没有直接关系,故选C。第4段首句的胸腺嘧啶的变异和吸烟者发生肺癌的机会呈正相关;而根据第2段首句可知,胸腺嘧啶存在于chromosome 15,也属于基因变异这一系列的事实,可推出A、B符合文意;D与第4段倒数第2句中的smoking promotes cancer相符。
单选题 The results of the study done by Paul Brennan and Christopher Amos ______.
【正确答案】 B
【答案解析】[解析] 第5、6段提到Paul Brennan和Christopher Amos所做的研究与deCODE公司结果的一些不同之处和相似之处,并在第6段末句总结得出,实际情况可能更加复杂,B符合此意,故正确。A中的completely太绝对;C中的instead of与第6段倒数第2句中的involved as well不符;第5段第2句中的rather than否定了…modifying his smoking behavior,故D错误。
单选题 The current conclusions drawn from the studies have been ______.
【正确答案】 C
【答案解析】[解析] 最后两段对原文提到的研究所得的结论做了总结评价,其中倒数第2段首句提到这些研究既puzzling又intriguing,而末段首句又提到这些研究raises interesting issues,且该段第2句又说到对问题更深入理解的一天“近在咫尺”。由此可知,作者认为这些研究的结果是很具启发性的,故选C。A和B的disappointing和frustrating属于贬义,通读全文可知作者并未在文中表达出贬义的感情色彩;文中提到了两个产生对立结论的研究,并表明还有问题没有确定,可见研究的结论不全面,故D“综合性的,全面的”不对。
单选题 Which of the following is INCORRECT about the study of genetics?
【正确答案】 A
【答案解析】[解析] 第7段首句确实提到了布伦南和阿莫斯教授均采用了和deCODE公司不同的研究方法,但第6段首句提到他们均确定rs1051730是一个重要的单核苷酸多态性结构,这一点与deCODE公司观点一致,说明两个研究也存在相同之处,故A中的第二个different表述不对,因此选A。