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UNIVERSE SEEKERS

WELCOME TO OUR UNIVERSE A Site where you can find astounding discoveries made by our own race. UNIVERSE SEEKERS offers differen...

UNIVERSE SEEKERS

WELCOME TO OUR UNIVERSE


A Site where you can find astounding discoveries made by our own race.

UNIVERSE SEEKERS offers different topics for you to read.

-SCIENCE
-MATHEMATICS
-LITERATURE
-HISTORY
-TECHNOLOGY
-CONSPIRACIES
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How to Clone Yourself

•How to Clone Yourself
By: SMice

Image result for cloning


Teka bgo ko simulan.Alam ko lahat tyo gusto maclone ang sarili ntn.Pero itatanong ko sainyo?Ano ba nsa isip mo if heard that word?Syempre Human Cloning! Well sadly hindi to pang human kundi a basic procedure ng cloning on your DNA.
have you ever heard this "Polymerase Chain Reaction" if yes hindi ka mawawala dto so lets proceed.
When molecular biologists use the term "cloning," they are usually referring to the process of cloning a gene,not an organism. If you want to clone yourself, start small by cloning a gene. You might find something interesting.

Studying a single gene and the protein or proteins it encodes is hampered by the fact that genes exist in a bustling genome. It is often useful to isolate a gene so that it can be studied or manipulated in isolation. For example, cloning the gene for human insulin allows us to produce large amounts of insulin in bacteria.
Cloning is easier than you might think. If you already have a gene in mind you can look it up in a sequenced genome! Let's say you want to clone your insulin gene to see if it's any different from your friend's. In the human genome, the gene for insulin is abbreviated INS and happens to sit on
chromosome 11.
The first step is to amplify the gene using a process called PCR, short for polymerase chain reaction. In PCR, short pieces of single-stranded DNA are used as primers to get the reaction going. One primer binds at the front of the gene and the other at the end. Together, they define the region of DNA your PCR reaction will copy,exponentially.
After PCR, you have a tube of DNA that is almost exclusively the INS gene. From here,you can sequence the gene directly by mailing away the INS PCR product (the routine method of DNA sequencing is very similar to PCR, requiring also one of your primers)

But say you are also interested in producing your own supply of insulin, encoded by your own personal INS gene. To do that,you need a cell that can read the instructions encoded in the INS gene to produce functional insulin protein. Luckily, all life on earth uses a shared genetic code and so a gene from one organism can be understood by any other organism. E. coli is usually the first choice,since it grows quickly and is easy to handle.

First you need to figure out a way to get INS into E. coli. The cell needs more instructions than what is encoded in this foreign, human gene, and the DNA needs a vehicle to carry it into the cell.
The solution is to use a plasmid. Plasmids are small, circular molecules of DNA that bacteria faithfully copy before each cell division. The plasmids are easily taken up by bacteria using a simple heat shock procedure, and they stick around because they encode a gene for antibiotic resistance, Growing the bacteria on the corresponding antibiotic means that only the cells with the plasmid can survive.

Here's where the cloning comes in. Youinsert your INS gene into the plasmid using restriction enzymes. When you transfer the plasmid to E. coli, the cells will produce many copies of the plasmid (and by extension your INS gene) with each cell division. It is this method of precise copying that we call "cloning."

Now, to finish this out you have to instruct the E. coli to express insulin. Though the cells understand the coded message for assembling insulin, they do not have the same machinery as humans to recognize that there is a message to be read! By adding a suitable genetic switch you create what is now called an expression plasmid (or, more commonly, "expression vector.")

As the E. coli cells grow, they faithfully copy your plasmid and express the insulin encoded in your INS gene. With the right biochemical know-how, you can purify this small, cloned part of yourself.
What's truly remarkable about this method of cloning is that you can apply it to any gene you want, although very long genes are tricky to clone.

So now you've cloned a small part of you. In fact, we could say you cloned the smallest unit of you: one gene.

(c) Scitable

~Smice

Agent P's Genome

•AGENT P's GENOME•
By: Dren


Agent P,the alias also of the pet of Phineas and Ferb na si PERRY THE PLATYPUS.But have you ever wonder on their Genome?Do they share some characteristics with other animals?Humans? Also this is also one very interesting example of the topic we discussed recently on Systematics.Lets find out.



The sequencing of the platypus genome has received a high amount of misleading press attention.What does this information really tell us about this strangely unique animal and its genetic past?

The recent publication of a draft of the platypus genome (Warren et al., 2008) has garnered a great deal of newspaper coverage, much of which has been misleading. Over and over again, the article lead is that the platypus is "weird" or "odd," or even worse, that the animal is a chimera.
One author, for instance, describes the platypus as a "genetic potpourri—part bird, part reptile, and part lactating mammal" (AFP, 2008). Unfortunately, such statements are inaccurate. In reality, the platypus is not part bird, as birds are an independent and (directly) unrelated lineage.
Moreover, although one could say that the platypus is part reptile, it is so only in the sense that it is a member of the great reptilian clade that also includes prototherians, marsupials, birds, lizards,snakes, dinosaurs, and eutherian mammals (including humans). Using this line of reasoning, we humans could say with equal justification that we, too, are part reptile.
For what we know they are MAMMALS that LAYS EGG which is an unique one talaga.
The truth about the platypus—and what makes the animal's recent genomic sequencing particularly m interesting—is that it belongs to a lineage that separated from ours approximately 166 million years ago,deep in the Mesozoic era, and since that time, it has independently lost different elements of our last common ancestor. By comparing bits of the platypus genome that were conserved with those that were lost, researchers can develop a clearer picture of what Jurassic mammals were like, and they can also determine what sorts of genetic traits contemporary mammals have gained and lost over the course of evolution.
In order to better understand the impact of the platypus study, it is helpful to begin by looking at a cladogram that illustrates the dates when derived traits
appeared in the various lineages considered in the study (Nasa Comment Section). This diagram reflects a fairly conventional picture of our evolutionary history, and it reinforces the evolutionary explanation for the illustrated relationships.As you can see, a number of modern animals-including birds-are depicted along the top of the cladogram in Figure 1. Note,however, that the cladogram does not imply that modern monotremes (including the platypus) are part bird. Rather, birds are included in this diagram because they are contemporary representatives of the sauropsid lineage, a group of reptile cousins
that split from our family tree roughly 315 million years ago. So, if monotremes aren't part bird, why did the investigators who conducted the platypus study examine genomic data from chickens during the course of their research? The primary reason for inclusion of this data relates to comparison.Specifically, the researchers knew that if they found a feature in birds that was also present in monotremes (or marsupials or eutherians), this would mean that the feature was most likely also present in the animals' common ancestor.
For instance, one of the unusual (for a mammal) features of the platypus is
meroblastic cleavage. In fact, there is a famous telegram from 1884 in which researchers who were working in Australia announced a dramatic discovery to their colleagues at the British Association:
"Monotremes oviparous, ovum meroblastic."
Those four words declare that the platypus lays eggs (i.e., it is oviparous) and that the early stages of platypus embryo formation resemble the stages seen in birds and reptiles, not mammals. As opposed to the platypus, eutherians and marsupials have eggs that go through holoblastic cleavage; this means that the first cell divisions following fertilization cut all the way through the ovum,producing multiple,separable daughter cells. On the other hand,in the meroblastic cleavage of the platypus and chicken, the large yolky egg does not completely subdivide, so early cell divisions are incomplete. These incomplete divisions produce a sheet of cells on top of the yolk that are cytoplasmically continuous with the yolk cytoplasm. Indeed, this sheet is common feature in yolky eggs and is a
consequence of physical constraints on cell division.
Thus, both the platypus and the chicken exhibit meroblastic cleavage—but this does not mean that platypuses are part bird.Rather, what it does suggest is that
meroblastic cleavage is likely a primitive character, one that was inherited from thelast common ancestor of synapsids and sauropsids over 300 million years ago.Another possibility is that birds and monotremes evolved this feature independently, thereby making this trait an example of convergent evolution. Simple observation of meroblastic cleavage in both monotremes and birds is not enough to determine whether this characteristic arose via convergence or via common descent—in order to discover which is the case, we must look at multiple details of the evolutionary process.
Of course, not just the platypus but every living organism is a mix of both conserved,primitive characters and evolutionary novelties—thus, a mouse is just as "weird" as a platypus from an evolutionary perspective, as each is the product of processes that promoted divergence from a common ancestor, and each is equidistant from that ancestor. It's just that we primates share more derived characters, or synapomorphies, with mice than with platypuses because we are more closely related, and the mix of characters in mice istherefore more familiar to us.
Indeed, all modern animals are products of different evolutionary trajectories, and no one species by itself is representative of the ancestral condition. As a result, we must determine the ancestral state of modern animals through the comparison of multiple lineages—and that is the virtue of the data from the platypus. Information regarding the platypus genome adds yet another lineage to our data set—a lineage that diverged from ours over 160 million years ago. The platypus data is therefore a lens that can help us see what novelties arose during that 160 million year window on both the eutherian and monotreme sides of the split.
Sequencing of the platypus genome reveals that the platypus has about 18,000 genes; humans, by comparison, have somewhere around 20,000.Moreover, roughly 82% of the platypus's genes are shared between monotremes,marsupials, eutherians, birds, and reptiles. This is not at all surprising,because all of these organisms are made of eukaryotic cells, and the basic eukaryotic machinery is going to be shared among species. Platypuses and humans also share a lot of "selfish" DNA bits—about half of both species' genomes consists of LINE and SINE - like sequences.
Humans and platypuses do differ in the details, however. For instance, an obvious difference is that the platypus lays yolky eggs, whereas humans and other eutherians have yolkless eggs that are retained in the mother's body. Thus, as you might expect,the platypus has a gene that humans lack—one that codes for vitellogenin, a crucial yolk protein.

Source
•AFP. Neither fish nor fowl: Platypus genome
decoded. May 7 (2008)
•Brown, S. Top billing for platypus at end of
evolution tree. Nature News 453, 138 (2008)
~Dren