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{"id":197,"date":"2015-01-19T07:23:52","date_gmt":"2015-01-19T14:23:52","guid":{"rendered":"http:\/\/www.thinkbio.guru\/tBioWordPress\/?p=197"},"modified":"2017-04-12T13:52:21","modified_gmt":"2017-04-12T17:52:21","slug":"evolution-introductory-biology-cellmolecular-semester","status":"publish","type":"post","link":"https:\/\/www.thinkbio.guru\/tBioWordPress\/2015\/01\/evolution-introductory-biology-cellmolecular-semester\/","title":{"rendered":"Evolution in Introductory biology: cell\/molecular semester"},"content":{"rendered":"<p><a href=\"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-content\/uploads\/2015\/01\/Depositphotos_10405184_xs.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignright size-full wp-image-631\" src=\"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-content\/uploads\/2015\/01\/Depositphotos_10405184_xs.jpg\" alt=\"Giant galapagos turtle\" width=\"200\" height=\"256\" \/><\/a>Many institutions divide Introductory Biology into Cell\/Molecular and Ecology\/Evolution semesters. There is some sense to this, in that one scale <em>can be seen as<\/em>\u00a0cellular and smaller, the other organismal and larger. However, failing to weave the influences, evidences and implications of evolution into the cell-molecular semester wastes an opportunity to show students through our teaching of these topics how central these ideas are. Further, there are a wonderful molecular examples that represent powerful, approachable proofs and demonstrate to students what they can do if they pick up these tools.<\/p>\n<p><!--more--><\/p>\n<p>With a topic as broad as Evolution in Introductory Biology, I&#8217;m going to be a disperse in my discussion, though the curriculum I teach has what I think is a reasonably cohesive presentation for students. Many of the elements I use are dealt with in other blog posts or in materials I have posted\/hope to post from my <a title=\"thinkBio lecture components: references, powerpoints, outlines...\" href=\"https:\/\/thinkbio.guru\/LectComponents\/All_Lect_Table.html\" target=\"_blank\">Lecture Components<\/a>\u00a0(disclaimer: because of copyright challenges, I&#8217;m going to have to core out textbook figures from PowerPoints, and replacing them is sloooow work).<\/p>\n<h2>Overview: method to the madness<\/h2>\n<p>I&#8217;ll start with negation: I think integration\u00a0<em>doesn&#8217;t<\/em> work when the &#8216;unit&#8217; on evolution is a unit on evolution. We need to integrate evolutionary thinking into what we&#8217;re already working to teach. Since evolutionary processes gave rise to, oh, pretty much everything we share with students, the challenge is more one of identifying cases that are interesting and apparent than of going to exotic depths to fit something in. While there are tons of fun things to discuss that fit into that &#8216;other semester&#8217; of Introductory Biology, I don&#8217;t think there&#8217;s a need to poach, and I think it can ring hollow: &#8220;If this is so true and so central, why don&#8217;t we talk about cells and molecules in this context?&#8221;. Further, one of the great straw men\u00a0of those seeking to deny evolution through confusion are the arguments about &#8216;irreducible complexity&#8217; or Answers in Genesis&#8217; claims about &#8220;changes within kinds are OK, but &#8216;molecules to man&#8217; is a different class of thing.&#8221;<\/p>\n<p>So my goal will be identifying instances where evolutionary evidence and thinking can be gracefully integrated with general topics in Cell\/Molecular introductory biology (that I agree with \ud83d\ude1b ).<\/p>\n<h2>Specific Cases for Evolution in Introductory Biology<\/h2>\n<h4>Endosymbiont theory: Stealing is easier than inventing<\/h4>\n<p><a href=\"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-content\/uploads\/2015\/01\/Depositphotos_8020098_xs.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignright wp-image-634 size-full\" src=\"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-content\/uploads\/2015\/01\/Depositphotos_8020098_xs.jpg\" alt=\"Eukaryotic cell\" width=\"256\" height=\"255\" srcset=\"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-content\/uploads\/2015\/01\/Depositphotos_8020098_xs.jpg 256w, https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-content\/uploads\/2015\/01\/Depositphotos_8020098_xs-150x150.jpg 150w\" sizes=\"auto, (max-width: 256px) 100vw, 256px\" \/><\/a>I love the Endosymbiont theory. It&#8217;s an opportunity to accomplish so many things in one place, so is a great way to deliver on my goal of using <a title=\"One ring to rule them all: teaching content through themes\" href=\"http:\/\/www.thinkbio.guru\/tBioWordPress\/2014\/09\/one-ring-rule-teaching-content-themes\/\" target=\"_blank\">Themes<\/a> to unite Intro Bio teaching. I use it as part of a discussion on prokaryotes vs. eukaryotes and as a lead-in to a discussion of organelles, because the\u00a0<em>origins<\/em> of mitochondria and chloroplasts provide an explanation for their membrane-bound structure (the outermost membrane, that is). And Lynn Margulis is credited for origination of the theory, so it&#8217;s an opportunity to quietly point out that women in science is a thing. But for this post, the Big Deal is\u00a0<em>how the argument for the theory is made.<\/em>\u00a0I love being able to defend the claim on the basis of differing branches of evidence, allowing me to point out what a scientific\u00a0<strong>theory<\/strong>\u00a0is, as opposed to a hypothesis.<\/p>\n<p>I lead with a <a title=\"Phagocytosis cartoon from St. Olaf\" href=\"www.stolaf.edu\/people\/giannini\/flashanimat\/cellstructures\/phagocitosis.swf\" target=\"_blank\">cartoon about phagocytosis<\/a>. Without going over-deep with students at what is (for me) an early part of the semester, I generally introduce the ideas as\u00a0<em>categories:<\/em> &#8220;like-prokaryote&#8221; and &#8220;like eukaryote&#8221;. Note that as this proceeds, it&#8217;s an opportunity to casually keep referring to some structural elements of the mitochondria of eukaryotic cells:<\/p>\n<ul>\n<li>DNA: Circular (like-prokaryote)<\/li>\n<li>outer membrane: like-eukaryote<\/li>\n<li>inner membrane: like-prokaryote (see <a title=\"Wikipedia on cardiolipin\" href=\"http:\/\/en.wikipedia.org\/wiki\/Cardiolipin\" target=\"_blank\">cardiolipin<\/a>)<\/li>\n<li>chromosome structure: circular (like-prokaryote)<\/li>\n<li>genes: structure, homologies (like-prokaryote)<\/li>\n<li>ribosomes: structure, sequence (like-prokaryote)<\/li>\n<\/ul>\n<p>The evolutionary focus is one that I&#8217;ll weave as a theme throughout the course: it&#8217;s easier to copy (or in this case, flat out\u00a0<em>steal<\/em>\u00a0) than to create-from-scratch. We&#8217;ll be re-visiting this idea when we look at DNA and at the globin and opsin gene families (see below). But note how there is an opportunity to integrate domains of life (I don&#8217;t focus much on archaea vs. bacteria here [except that one is the engulfer; one the engulfee!], but we cover prokaryote vs. eukaryote nicely), theory vs. hypothesis, organelles, membranes, forms of evidence, and the Endosymbiont theory itself, which is often on to-do lists.<\/p>\n<p>Apropos of nothing above, note that there is currently a challenge to the &#8220;the archaea\u00a0tried to eat a prokaryote but kept it as an organelle&#8221; version that proposes that the <a title=\"Phylogenetic argument for parasitic origin of mitochondria\" href=\"http:\/\/journals.plos.org\/plosone\/article?id=10.1371\/journal.pone.0110685\" target=\"_blank\">prokaryote was a parasite instead<\/a>. Of course, the evidence is sequence alignments and tree-thinking :-).<\/p>\n<h4>Got globin? alpha, beta, gamma, other, and dead globin genes<\/h4>\n<p>A huge component of the lab arm that accompanies the Intro Bio course I&#8217;ve been involved in is an <a title=\"Investigating how hemoglobin works\" href=\"https:\/\/thinkbio.guru\/Molecules\/Hemoglobin.html\" target=\"_blank\">exploration of structure-function of hemoglobin<\/a>. Besides the blatant homology of myoglobin and alpha and beta hemoglobin (not dealt with very explicitly in the tutorial, but see this <a title=\"Davidson website on hemoglobin evolution &amp; homologies\" href=\"http:\/\/www.bio.davidson.edu\/Courses\/Molbio\/MolStudents\/spring2010\/Hua\/Orthologs.html\" target=\"_blank\">website from Davidson<\/a>) the latter tutorial &#8216;pages&#8217; take up the differences between fetal (gamma) hemoglobin, including\u00a0<em>what<\/em>\u00a0one of the critical amino acid changes is and\u00a0<em>how<\/em> this enables us to be mammals&#8211;letting the fetus (a.k.a. parasite within) &#8216;steal&#8217; oxygen from its same-species (and basically same genotype) mother.<\/p>\n<p>Of course, the greatest way to &#8216;knit&#8217; evolutionary aspects into hemoglobin discussions and to build bridges between the two semesters of Intro Bio is sickle cell anemia (see appropriate links <a title=\"Table including sickle cell anemia links\" href=\"https:\/\/thinkbio.guru\/3D_Directory\/!HemoTable.html\" target=\"_blank\">here<\/a>). The fact that sickle cell anemia alleles provide <em>resistance<\/em> to malaria explains the prevalence of these\u00a0alleles in populations where malaria has historically\u00a0been a horrific killer. Rather than going into further depth here, I&#8217;ll link to my <a title=\"One ring to rule them all: teaching content through themes\" href=\"http:\/\/www.thinkbio.guru\/tBioWordPress\/2014\/09\/one-ring-rule-teaching-content-themes\/\">Hemoglobin blog post<\/a> and try to supplement it &#8216;someday&#8217; with more on\u00a0malaria, hemoglobinopathies, genetic linkage (it&#8217;s how we know sickle cell anemia arose several times independently; this is challenging to show bc it&#8217;s always the same mutation!). You can also read Sean Carroll&#8217;s wonderful &#8216;<a href=\"https:\/\/www.thinkbio.guru\/tBioWordPress\/2015\/01\/book-review-making-fittest\/\">Making of the Fittest<\/a>.&#8217;<\/p>\n<h4>The making of DNA: better than but derived from RNA<\/h4>\n<p>I have an existing <a title=\"thinkBio lecture components on cytosine, uracil, thymine\" href=\"https:\/\/thinkbio.guru\/LectComponents\/CytUraThy.html\">lecture compilation<\/a> on this deep, wonderful topic so I&#8217;ll bare bones it here. Briefly put, a ton of evidence indicates that &#8216;RNA came first,&#8217; but RNA has several Achille&#8217;s heels. While I hope we never settle for &#8216;memorize these differences&#8217;, the full discussion can take a couple thoughtful class periods\u00a0to navigate. I think it&#8217;s worth it, because they&#8217;re\u00a0so darn readily understood if explained well! The 2&#8217;OH position is dangerous (in a way that is related to the mechanisms of ATPases!), but the fix takes some hard-won reducing power. The <em>reason for<\/em> the\u00a0difference between uracil and thymine originates with&#8230; the stupidity of using cytosine?!? Briefly, cytosine reacts with water to yield uracil&#8230; which is terribly &#8216;misleading&#8217; in an informational system based on Ade, Cyt, Gua, <span class=\"text-danger\"><strong>Ura<\/strong><\/span>. The &#8216;obvious&#8217; solution is to replace\u00a0<em>cytosine<\/em>; but that&#8217;s often not how evolutionary processes work&#8211;a sufficient &#8216;findable&#8217; solution, however ugly (and boy, is this one ugly&#8211;se the lecture compilation, but it entails an energetically expensive redox reaction [add -CH3] on EVERY &#8216;uracil&#8217; to create Thy, de-energizing accidentally created dUTP, stripping dUTP out of DNA [which still occurs bc the chemical change Cyt =&gt; Ura still happens!] etc. The very ugliness of the &#8216;fix&#8217; that is DNA lets us clearly argue that evolution is\u00a0<em>not<\/em> some &#8216;magic wand&#8217; that creates &#8216;best solutions&#8217;, lets us argue against &#8216;foresight&#8217; in evolution, and lets students think deeply about &#8216;accessible solutions&#8217; in a concrete way.<\/p>\n<p>Overall, therefore, I think this challenging discussion is well worthwhile, and it leaves students with an understanding of WHY DNA contains 2&#8242; -H instead of -OH and employs thymine instead of uracil.<\/p>\n<h4>Opsins and color vision: easy come, easy go?<\/h4>\n<p>This is a neat story (actually, a series of related ones) that very much fits into an Intro Bio course that has an emphasis on molecular understanding. You can use\u00a0<a href=\"https:\/\/thinkbio.guru\/Molecules\/Opsin.html\">thinkBio&#8217;s resources<\/a> (rather, the current state of sharing them \ud83d\ude42 ). Fantastic coverage of some of the data and some of the stories can be found in Sean Carroll&#8217;s &#8216;<a title=\"link to text 'Making of the Fittest'\" href=\"http:\/\/seanbcarroll.com\/the-making-of-the-fittest\/\" target=\"_blank\">Making of the Fittest<\/a>&#8216; (which provides a number of cases that would fit right into this post, and does a great job of collating\u00a0useful resources). Since opsin is worthy of (and will someday receive) its own blog post, I&#8217;ll bullet my way through this:<\/p>\n<ul>\n<li>tree thinking throughout: deduction of the loss of tri-chromatic vision when early mammals &#8216;went dark&#8217; (nocturnal), and the homology evidence that indicates we duplicated our &#8216;red&#8217;\u00a0opsin to make a\u00a0&#8216;green&#8217;<\/li>\n<li>DNA sequencing and its relevance: the evidence that we &#8216;re-created&#8217; a green\u00a0from a\u00a0red is based on the greater sequence homology between our green and our red vs. our green and greens of reptiles, etc.<\/li>\n<li>how evolutionary processes &#8216;discover&#8217;\/&#8217;invent&#8217; new things: by copying and modifying old things<\/li>\n<li>structure\/function: by changing the\u00a0<em>environment<\/em> of the retinal co-factor (which actually absorbs the photons), opsin shifts peak light absorbance (thus the\u00a0<em>protein<\/em> determines the &#8216;red or green [or blue]&#8217; behavior of the retinal<\/li>\n<li>if you go this\u00a0route&#8230; opsin is coupled to a G-protein coupled receptor, which is part of a <a title=\"Wikipedia on phototransduction\" href=\"http:\/\/en.wikipedia.org\/wiki\/Visual_phototransduction\" target=\"_blank\">cellular signaling pathway,<\/a> which triggers a nerve signal (and an insight into &#8216;how things work&#8217;&#8211;the signal is generated constantly\u00a0<em>in the dark<\/em>, and &#8216;I saw light&#8217; is signaled by an\u00a0<span style=\"text-decoration: underline;\">interruption<\/span> in that signal<\/li>\n<\/ul>\n<h4>Jeepers, creepers, where&#8217;d you get those peepers?<\/h4>\n<p>Currently, we only know of a <a title=\"thinkBio blue eyes evidence\" href=\"https:\/\/thinkbio.guru\/LectComponents\/Blue_eye_origins.html\" target=\"_blank\">single origin<\/a> of the alleles for blue eyes.\u00a0<strong>How<\/strong> do we know this? Because all blue-eyed people (in the not-exhaustive study that was done; see previous link in this paragraph) have the exact same mutation. Given that we expect a large &#8216;target size&#8217; (there should be many ways to knock out melanin synthesis in the eye), it is conspicuous that everybody has the same one. This is a fun classroom discussion, because it&#8217;s\u00a0<em>about<\/em> the students themselves. And you get to call them mutants :-). You can also discuss sexual selection (I use data from dating sites that indicates a disproportionate number of people are seeking blue-eyed mates) and how it overrides potential deleterious effects (blue-eyed people are more likely to suffer eye damage over time). If desired, this whole discussion can be tied into melanin production (which is about both an enzyme pathway and vesicles\/cell biology).<\/p>\n<h4>Discovering milk&#8230; as adults<\/h4>\n<p>Another favorite story of mine, which currently has <a title=\"thinkBio lecture resources on lactase persistence\" href=\"https:\/\/thinkbio.guru\/LectComponents\/Lact_Persist_Summ.html\" target=\"_blank\">lecture resources<\/a>, but which deserves more from this site. This story \u00a0ties in with the tale of the origin of blue eyes, since it&#8217;s\u00a0a\u00a0counter-case: multiple origins of the trait as evidenced by different individuals bearing different alleles (DNA sequences). You can also link to a discussion of the lac operon (if that&#8217;s part of your curriculum): just as E. coli should not waste energy produce lac-digesting machinery, (most) mammals\u00a0don&#8217;t bother with\u00a0lactose after infancy (lactose intolerance)&#8230; All this changed when\u00a0we domesticated other mammals and (for whatever reason!) tried their milk. Portable dairies (and butcher shops) were clearly a major innovation, as evidence shows &#8216;lactase persistence&#8217; (production of lactose-digesting enzymes into adulthood) had\u00a0multiple origins, likely correlated with domestication of camels in some cases, cows in others (again, see link for resources).<\/p>\n<h4>More, more, more!<\/h4>\n<p>The theme of &#8216;<a title=\"thinkBio materials for evolution and deduction in IntroBio\" href=\"https:\/\/thinkbio.guru\/LectComponents\/Honors_DNA_Origins.html\" target=\"_blank\">Deduction of evolutionary history through sequence homology<\/a>&#8216; makes for an\u00a0Honors course that goes\u00a0as follows:<\/p>\n<ol>\n<li>Phylogenetic trees and deduction (one can use AIDS history, or tamiflu resistance, or&#8230;). This ties to an in-class exercise where students &#8216;mutate&#8217; and form a tree. Count total mutations in the &#8216;historical&#8217; tree immediately after formation; then create a random tree (everyone takes\u00a0up an arbitrary position in the tree) and observed vastly more apparent mutations between parents-and-children in the &#8216;wrong&#8217; tree<\/li>\n<li>Blue eyes<\/li>\n<li>Lactose intolerance\/lactase persistence<\/li>\n<li>Multiple origins of sickle cell (how can we deduce this given that there is only 1 mutation that\u00a0<strong>can<\/strong> cause sickle cell anemia? Mustn&#8217;t it therefore always present like blue eyes? A.: No. <a href=\"https:\/\/en.wikipedia.org\/wiki\/Genetic_linkage\"><em>L<\/em><em>inkage<\/em><\/a> allows us to include large swaths of flanking DNA that can be looked at as &#8216;islands&#8217; flowing through time)<\/li>\n<li>Corgis, dachshunds, basset hounds. This one is complex, but a great capstone investigation\/discussion. The causative mutation is unimaginably rare: dominant mutation caused by reverse transcription (as evidenced by intron elimination) and re-insertion leading to over-expression of the cDNA. Interesting because it&#8217;s a mimic of human phenotypes. The obvious prediction is that this must be the &#8216;blue eyed case&#8217; of single common origin. But in a &#8216;phylogenetic tree of dogs&#8217; [for which there is a lot of great data], the species mentioned above\u00a0<em>are on distant branches!?!?<\/em> Resolution: this mutation was on a deep ancestor, and\u00a0<em>pools<\/em> of dogs were split off to give different breeds. At the time of the splitting, this allele was included in each of the relevant pools. It was later lost in some breeds, but &#8216;locked into&#8217;\u00a0others.<\/li>\n<\/ol>\n<h4>When I am braver&#8230;<\/h4>\n<p>I&#8217;ll open up the comments, because I think this topic is incredibly important, and we have just as many opportunities to discuss evolution in introductory biology, its footprints, mechanisms, and processes during the Cell\/Molecular semester of IntroBio as colleagues do in the Evo\/Eco semester.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Many institutions divide Introductory Biology into Cell\/Molecular and Ecology\/Evolution semesters. There is some sense to this, in that one scale can be seen as\u00a0cellular and smaller, the other organismal and [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[26,12,7,16,11,14,8],"tags":[],"class_list":["post-197","post","type-post","status-publish","format-standard","hentry","category-ap-biology","category-evolution","category-hemoglobin","category-lecture-modules","category-opsin","category-organelles","category-themes"],"_links":{"self":[{"href":"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-json\/wp\/v2\/posts\/197","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-json\/wp\/v2\/comments?post=197"}],"version-history":[{"count":3,"href":"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-json\/wp\/v2\/posts\/197\/revisions"}],"predecessor-version":[{"id":866,"href":"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-json\/wp\/v2\/posts\/197\/revisions\/866"}],"wp:attachment":[{"href":"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-json\/wp\/v2\/media?parent=197"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-json\/wp\/v2\/categories?post=197"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.thinkbio.guru\/tBioWordPress\/wp-json\/wp\/v2\/tags?post=197"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}