The Human Genome: Copied by Design | Fazale Rana

humangenome

This is a WordPress repost of an excellent article on research being done on the Human Genome that was originally authored by Fazale Rana. 

Fazale Rana was formerly a senior scientist in research and development at Procter & Gamble, Fuz graduated with highest honors from West Virginia State College (now University) with a BS in chemistry and went on to earn a PhD in chemistry with an emphasis in biochemistry from Ohio University, where he was twice awarded the Donald Clippinger Research Award. He pursued postdoctoral studies in the biophysics of cell membranes at the Universities of Virginia and Georgia.

Several articles by Fuz have been published in peer-reviewed scientific journals – such as Biochemistry, Applied Spectroscopy, FEBS Letters, Journal of Microbiological Methods and Journal of Chemical Education – and he has delivered numerous presentations at international scientific meetings. He also holds two patents, authored a chapter on molecular convergance and intelligent design for The Nature of Nature, and co-wrote a chapter on antimicrobial peptides for Bilogical and Synthetic Membranes.

Biochemist Fazale (Fuz) Rana writes and speaks extensively about evidence for creation emerging from biochemistry, genetics, human origins, and synthetic biology. As vice president of research and apologetics at Reasons to Believe (RTB), he is dedicated to communicating to skeptics and believers alike the powerful scientific case for God’s existence and the Bible’s reliability.


The time my wife Amy and I spent in graduate school studying biochemistry were some of the best days of our lives. But it wasn’t all fun and games. For the most part, we spent long days and nights working in the lab.

But we weren’t alone. Most of the graduate students in the chemistry department at Ohio University kept the same hours we did, with all-nighters broken up around midnight by “Dew n’ Donut” runs to the local 7-Eleven. Even though everybody worked hard, some people were just more productive than others. I soon came to realize that activity and productivity were two entirely different things. Some of the busiest people I knew in graduate school rarely accomplished anything.

This same dichotomy lies at the heart of an important scientific debate taking place about the meaning of the ENCODE project results. This controversy centers around the question: Is the biochemical activity measured for the human genome merely biochemical noise or is it productive for the cell? Or to phrase the question the way a biochemist would: Is biochemical activity associated with the human genome the same thing as biochemical function?

The answer to this question doesn’t just have scientific implications. It impacts questions surrounding humanity’s origin. Did we arise through evolutionary processes or are we the product of a Creator’s handiwork?

The ENCODE Project

The ENCODE project—a program carried out by a consortium of scientists with the goal of identifying the functional DNA sequence elements in the human genome—reported phase II results in the fall of 2012. To the surprise of many, the ENCODE project reported that around 80% of the human genome displays biochemical activity, and hence function, with the expectation that this percentage should increase with phase III of the project.

If valid, the ENCODE results force a radical revision of the way scientists view the human genome. Instead of a wasteland littered with junk DNA sequences (as the evolutionary paradigm predicts), the human genome (and the genomes of other organisms) is packed with functional elements (as expected if a Creator brought human beings into existence).

Within hours of the publication of the phase II results, evolutionary biologists condemned the ENCODE results, citing technical issues with the way the study was designed and the way the results were interpreted. (For a response to these complaints go herehere, and here.)

Is Biochemical Activity the Same Thing As Function?

One of the technical complaints relates to how the ENCODE consortium determined biochemical function. Critics argue that ENCODE scientists conflated biochemical activity with function. For example, the ENCODE Project determined that about 60% of the human genome is transcribed to produceRNA. ENCODE skeptics argue that most of these transcripts lack function. Evolutionary biologist Dan Graur has asserted that “some studies even indicate that 90% of transcripts generated by RNA polymerase II may represent transcriptional noise.”In other words, the biochemical activity measured by the ENCODE project can be likened to busy but nonproductive graduate students who hustle and bustle about the lab but fail to get anything done.

When I first learned how many evolutionary biologists interpreted the ENCODE results I was skeptical. As a biochemist, I am well aware that living systems could not tolerate such high levels of transcriptional noise.

Transcription is an energy- and resource-intensive process. Therefore, it would be untenable to believe that most transcripts are mere biochemical noise. Such a view ignores cellular energetics. Transcribing 60% of the genome when most of the transcripts serve no useful function would routinely waste a significant amount of the organism’s energy and material stores. If such an inefficient practice existed, surely natural selection would eliminate it and streamline transcription to produce transcripts that contribute to the organism’s fitness.

Most RNA Transcripts Are Functional

Recent work supports my intuition as a biochemist. Genomics scientists are quickly realizing that most of the RNA molecule transcribed from the human genome serve critical functional roles.

For example, a recently published report from the Second Aegean International Conference on the Long and the Short of Non-Coding RNAs (held in Greece between June 9–14, 2017) highlights this growing consensus. Based on the papers presented at the conference, the authors of the report conclude, “Non-coding RNAs . . . are not simply transcriptional by-products, or splicing artefacts, but comprise a diverse population of actively synthesized and regulated RNA transcripts. These transcripts can—and do—function within the contexts of cellular homeostasis and human pathogenesis.”2

Shortly before this conference was held, a consortium of scientists from the RIKEN Center for Life Science Technologies in Japan published an atlas of long non-coding RNAs transcribed from the human genome. (Long non-coding RNAs are a subset of RNA transcripts produced from the human genome.) They identified nearly 28,000 distinct long non-coding RNA transcripts and determined that nearly 19,200 of these play some functional role, with the possibility that this number may increase as they and other scientific teams continue to study long non-coding RNAs.3 One of the researchers involved in this project acknowledges that “There is strong debate in the scientific community on whether the thousands of long non-coding RNAs generated from our genomes are functional or simply byproducts of a noisy transcriptional machinery . . . we find compelling evidence that the majority of these long non-coding RNAs appear to be functional.”4

Copied by Design

Based on these results, it becomes increasingly difficult for ENCODE skeptics to dismiss the findings of the ENCODE project. Independent studies affirm the findings of the ENCODE consortium—namely, that a vast proportion of the human genome is functional.

We have come a long way from the early days of the human genome project. When completed in 2003, many scientists at that time estimated that around 95% of the human genome consisted of junk DNA. And in doing so, they seemingly provided compelling evidence that humans must be the product of an evolutionary history.

But, here we are, nearly 15 years later. And the more we learn about the structure and function of genomes, the more elegant and sophisticated they appear to be. And the more reasons we have to think that the human genome is the handiwork of our Creator.

Resources

Endnotes

  1. Dan Graur et al., “On the Immortality of Television Sets: ‘Function’ in the Human Genome According to the Evolution-Free Gospel of ENCODE,” Genome Biology and Evolution5 (March 1, 2013): 578–90, doi:10.1093/gbe/evt028.
  2. Jun-An Chen and Simon Conn, “Canonical mRNA is the Exception, Rather than the Rule,” Genome Biology 18 (July 7, 2017): 133, doi:10.1186/s13059-017-1268-1.
  3. Chung-Chau Hon et al., “An Atlas of Human Long Non-Coding RNAs with Accurate 5′ Ends,” Nature 543 (March 9, 2017): 199–204, doi:10.1038/nature21374.
  4. RIKEN, “Improved Gene Expression Atlas Shows that Many Human Long Non-Coding RNAs May Actually Be Functional,” ScienceDaily, March 1, 2017, www.sciencedaily.com/releases/2017/03/170301132018.htm.
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About

Disciple of Jesus, married to Peggy, with 5 grown up children, 6 grand children, ex-Canadian military and residing in beautiful Dartmouth, Nova Scotia, Canada. a.k.a. "Papa"

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Posted in Apologetics, Defending Christianity, Evolution, Intelligent Design, Science and the Bible
2 comments on “The Human Genome: Copied by Design | Fazale Rana
  1. Pete says:

    Wow! I wish I understood it better. My brilliant nephew is working on a human genome project to identify the DNA element that causes diseases, specifically diabetes, and being able to eliminate it from the body. He is, as I say, brilliant. I expect one day he may get a Nobel prize for his efforts. I am going to send this to him and see what he has to say about it. Thanks Bruce. Be blessed

  2. The Human Genome: Copied by Design | Fazale Rana | Reasoned Cases for Christ

    […]ACOs may sound quite a bit like well being upkeep organizations.[…]

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