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The Questions of Developmental Biology

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federal proscription <strong>of</strong> human cloning. Some <strong>of</strong> the reasons cited by scientists and ethicists<br />

against Robertson's human cloning arguments are:<br />

1. Cloning is not a good technique for giving couples a chance to have genetically related<br />

children,* for scientific reasons that include the following: (a) <strong>The</strong> resulting child would be<br />

genetically related to only one member <strong>of</strong> the couple (which could cause enormous problems with<br />

divorce and custody laws). (b) With a success rate so far from 100%, a woman could not produce<br />

enough oocytes for the procedure to have a good chance <strong>of</strong> success. (c) This high failure rate<br />

predicts that many cloned fetuses would abort or be born malformed. As Marie DiBerardino and<br />

Robert McKinnell, two <strong>of</strong> the pioneers <strong>of</strong> cloning, have pointed out, "In nearly 100% <strong>of</strong> the cases,<br />

[human cloning] would give rise to abnormal embryos and fetuses, almost all <strong>of</strong> which would<br />

abort. And what an atrocity if an abnormal child were born!" (DiBerardino and McKinnell 1997).<br />

2. Moral issues loom tremendous against the "spare parts" argument. A person cannot "own"<br />

another person; a clone might not wish to be used for spare parts. Scenarios that involve the<br />

creation <strong>of</strong> "brain-dead" clones kept "in storage" for spare parts are not acceptable to most <strong>of</strong> us<br />

(see Krauthammer 1998). In addition, using cloning in this manner would extend the already<br />

great social inequalities caused by differential access to medical care. Those with enough<br />

resources could use cloned body parts to extend their lives to an unprecedented duration, creating<br />

a situation wherein economic advantage becomes an overwhelming biological advantage.<br />

3. No one knows the community or personal harm in being raised by a genetically identical<br />

parent. Genetic uniqueness has always been assumed. (Or, as one student remarked, it's bad<br />

enough being told what to do by a regular parent.)<br />

4. Biologically speaking, clones are not "late-born twins." First, they fail the genetic definition <strong>of</strong><br />

identical twins, since their mitochondrial genes (derived from the eggs <strong>of</strong> different women) would<br />

be different. Second, they fail the embryological criteria for twins in that they are not derived<br />

from the same zygote and do not share the same uterus.<br />

5. <strong>The</strong> government already sets limits on procreation rights. (You cannot legally marry your<br />

sibling or your child, for instance.) It does so by consent <strong>of</strong> the government. A ban on human<br />

cloning would not be a new role for the government.<br />

<strong>The</strong> Society for <strong>Developmental</strong> <strong>Biology</strong> and other scientific societies have taken the stand that<br />

researchers should be allowed to study the early human embryo in attempts to understand<br />

diseases and development and to enhance fertility. <strong>The</strong>y also do not wish to block pharmaceutical<br />

companies from developing their products. However, these groups feel that we are not technically<br />

or morally prepared to start cloning human beings.<br />

*In earlier times, adoption <strong>of</strong> a niece or nephew was a fairly common means <strong>of</strong> raising a genetically related child. K. E.<br />

von Baer, for instance, was raised by his childless aunt and uncle.<br />

<strong>The</strong> Exception to the Rule: Immunoglobulin Genes<br />

While the rule is that the genome is the same in every cell in the body, some white blood<br />

cells that function as part <strong>of</strong> the immune system provide exceptions to that rule. <strong>The</strong> B<br />

lymphocyte ("B cell") is able to synthesize proteins called immunoglobulins that can function as<br />

antibodies. For decades, immunologists puzzled over how the immune system could possibly<br />

generate so many different types <strong>of</strong> antibodies. Could all the 10 7 different types <strong>of</strong> antibody<br />

proteins be encoded in the genome?

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