Paul Hardin (chronobiologist)

Last updated
Paul Hardin
Born (1960-09-14) September 14, 1960 (age 63)
Hazel Crest, Illinois
Nationality American
Alma mater Southern Methodist University
Indiana University
Brandeis University
AwardsAschoff-Honma Prize
Scientific career
Fields Genetics
Chronobiology
Institutions Texas A&M University
University of Houston
Doctoral advisor William H. Klein
Other academic advisors Michael Rosbash

Paul Hardin (born September 14, 1960) is an American scientist in the field of chronobiology and a pioneering researcher in the understanding of circadian clocks in flies and mammals. Hardin currently serves as a distinguished professor in the biology department at Texas A&M University. [1] He is best known for his discovery of circadian oscillations in the mRNA of the clock gene Period (per), the importance of the E-Box in per activation, the interlocked feedback loops that control rhythms in activator gene transcription, and the circadian regulation of olfaction in Drosophila melanogaster . Born in a suburb of Chicago, Matteson, Illinois, Hardin currently resides in College Station, Texas, with his wife and three children.

Contents

Academic career

Hardin earned his B.S. in biology at Southern Methodist University (SMU) in 1982. He then continued to pursue a Ph.D in genetics from Indiana University in 1987 with William H. Klein. He went on to conduct his postdoctoral research at Brandeis University under the supervision of chronobiologist Michael Rosbash. [2] From 1991 to 1995, Hardin worked as a professor at Texas A&M University, and from 1995 to 2005 at the University of Houston. Since 2005, Hardin has worked as a professor and researcher in the biology department at Texas A&M University. He teaches courses on introductory biology, molecular cell biology, and a graduate level class on biological clocks. He also serves as the director of the Texas A&M's Center for Biological Clocks Research and as faculty for the Texas A&M Institute for Neuroscience and PhD program in genetics. [1] In addition, Hardin was also actively involved in the Society for Research on Biological Rhythms; he served as the secretary in 2006, treasurer in 2010, and president in 2016. [3]

Research

Discovery of per mRNA cycling

In 1971, Ron Konopka, a geneticist at the California Institute of Technology, discovered the Period gene, which he found to be involved in the circadian clock of Drosophila. [4] In 1999, Paul Hardin discovered that per mRNA underwent strong circadian oscillations by exposing isolated wild-type per mRNA to a series of light-dark (LD) cycles followed by cycles of constant darkness (DD). [5] As a post-doctorate in the lab of chronobiologist Dr. Michael Rosbash, Hardin specifically noted that per mRNA levels in Drosophila brains fluctuate about 10-fold in a typical 24-hour light-dark cycle. Hardin further demonstrated that wild-type protein, PER, can rescue rhythmicity in the mRNA of an arrhythmic mutant of the per gene. His findings suggested that feedback of the PER protein regulates levels of per mRNA. [6] Hardin ultimately published his seminal work on the rhythmic nature of per mRNA in Drosophila in the journal Nature . This discovery led Hardin and other prominent members in the field of chronobiology to develop a model that describes the clock mechanism in Drosophila. This model is referred to as the Transcription Feedback Loop, which suggests that the translated protein provides negative feedback on the mRNA transcription of itself. [6]

Role of the E-box in per activation

In 1997, Hardin, with Haiping Hao and David Allen, analyzed the sequence of the per gene in Drosophila and found a 69-bp enhancer upstream of the gene. This enhancer sequence contained an E-box (CACGTG), which was determined to be necessary for high-level per transcription. [7] As E-boxes are typically bound by proteins containing a basic helix-loop-helix (bHLH) protein structural motif, the presence of an E-box in per led to the hypothesis that the proteins involved in circadian rhythms may contain a bHLH domain. This proved to be vital in establishing the function of the previously discovered CLOCK protein, which was known to play a role in circadian rhythms and contained a bHLH domain as well. This discovery also aided in the identification of the BMAL1 and CYCLE proteins as critical players in the circadian rhythms of mammalian and Drosophila circadian systems respectively. [7]

Circadian rhythms in olfaction

While teaching at the University of Houston, Hardin, along with fellow scientists Balaji Krishnan and Stuart Dryer, investigated circadian rhythms of olfaction in Drosophila . Previous experiments had shown that Drosophila antennae demonstrate circadian rhythms. However, the mechanism for circadian rhythms in the antennae was unknown. To determine the mechanism of rhythms in antennae, Hardin and his team kept wild-type and mutant flies, per01 and tim01, in 12:12 light-dark (LD) cycles and measured olfaction in the antennae with an electroantennogram (EAG), that measures the average output of an insect antenna to its brain for a given odor, over a 24-hour period. Only the wild-type flies demonstrated rhythmicity in the electrical activity, which indicated that circadian rhythms were present in the olfactory response. [8] In contrast, the mutants showed no cyclic activity. Therefore, Hardin's team discovered that circadian rhythms control the olfactory response in Drosophila antennae and his results were eventually published in Nature. [9]

Discovery of two interlocked feedback loops in circadian clock

In 1999, Hardin along with Nick Glossop and Lisa Lyons, conducted research on the specific role of Clk in the interlocked feedback loops present in Drosophila circadian oscillators. It was previously known that five genes ( per , tim , dbt , Clk , and cyc ) controlled circadian rhythms in Drosophila. The per-tim regulation mechanism was known at this time, though Clk regulation was not yet known. [10]

Hardin and his team conducted a series of experiments to identify the two interlocked feedback loops in the circadian mechanism of Drosophila. This means that the per-tim feedback loop connects to the Clk-cyc feedback loop, so that one loop has an effect on the other, and vice versa. They measured wild-type and mutant Clk mRNA levels to identify any changes in transcription levels. They observed that the PER-TIM complex suppresses transcription. They hypothesized that the Clk repressor was either the CLK-CYC complex itself or a repressor that was activated by CLK-CYC. They observed that the presence of active CLK and CYC resulted in the repression of Clk, while arrhythmic per mutants exhibited low levels of Clk. This evidence led them to propose the following model regarding two interlocked feedback loops: [11] [12]

  1. Late at night, PER-TIM dimers in the nucleus bind to and sequester CLK-CYC dimers. This interaction effectively inhibits CLK-CYC function, which leads to the repression of per and tim transcription and the de-repression of Clk transcription.
  2. As PER-TIM levels fall early in the morning, CLK-CYC dimers are released and repress Clk expression, thereby decreasing Clk mRNA levels by the end of the day.
  3. Concomitant with the drop in Clk mRNA levels (through CLK-CYC–dependent repression) is the accumulation of per and tim mRNA (through E-box–dependent CLK-CYC activation).
  4. The levels of CLK-CYC fall in the early evening, leading to a decrease in per and tim transcription and an increase in Clk mRNA transcription.
  5. A new cycle then begins as high levels of PER and TIM enter the nucleus and CLK starts to accumulate late at night.

In 2003, Hardin's team uncovered the second feedback loop associated with the circadian clock. vrille (vri) and Par Domain Protein 1 (Pdp1) encode related transcription factors whose expression is directly activated by dCLOCK/CYCLE. They show that VRI and PDP1 proteins feed back and directly regulate dClock expression. Thus, VRI and PDP1, together with dClock itself, comprise a second feedback loop in the Drosophila clock that gives rhythmic expression of dClock, and probably of other genes, to generate accurate circadian rhythms. [13]

Summary of major research contributions

Current research

Hardin's current research centers on the function of the circadian clock in Drosophila melanogaster. [19] One of Hardin's main research topics is understanding the mechanism behind the circadian rhythms in olfaction and gustatory physiology. His research also focuses on understanding the role of post-translational regulatory mechanisms in the feedback loop that set a 24-hour rhythm. Lastly, his lab has been working on identifying if the interlocked loops in the feedback mechanism function as a circadian oscillator or a clock output. [1] His most recent article discusses the conservation of the transcription feedback loop in not only Drosophila, but also in other animal species as well. [20]

Honors and awards

Related Research Articles

<span class="mw-page-title-main">Circadian rhythm</span> Natural internal process that regulates the sleep-wake cycle

A circadian rhythm, or circadian cycle, is a natural oscillation that repeats roughly every 24 hours. Circadian rhythms can refer to any process that originates within an organism and responds to the environment. Circadian rhythms are regulated by a circadian clock whose primary function is to rhythmically co-ordinate biological processes so they occur at the correct time to maximise the fitness of an individual. Circadian rhythms have been widely observed in animals, plants, fungi and cyanobacteria and there is evidence that they evolved independently in each of these kingdoms of life.

A circadian clock, or circadian oscillator, is a biochemical oscillator that cycles with a stable phase and is synchronized with solar time.

<span class="mw-page-title-main">CLOCK</span> Protein-coding gene in the species Homo sapiens

CLOCK is a gene encoding a basic helix-loop-helix-PAS transcription factor that is known to affect both the persistence and period of circadian rhythms.

Timeless (tim) is a gene in multiple species but is most notable for its role in Drosophila for encoding TIM, an essential protein that regulates circadian rhythm. Timeless mRNA and protein oscillate rhythmically with time as part of a transcription-translation negative feedback loop involving the period (per) gene and its protein.

Period (per) is a gene located on the X chromosome of Drosophila melanogaster. Oscillations in levels of both per transcript and its corresponding protein PER have a period of approximately 24 hours and together play a central role in the molecular mechanism of the Drosophila biological clock driving circadian rhythms in eclosion and locomotor activity. Mutations in the per gene can shorten (perS), lengthen (perL), and even abolish (per0) the period of the circadian rhythm.

In molecular biology, an oscillating gene is a gene that is expressed in a rhythmic pattern or in periodic cycles. Oscillating genes are usually circadian and can be identified by periodic changes in the state of an organism. Circadian rhythms, controlled by oscillating genes, have a period of approximately 24 hours. For example, plant leaves opening and closing at different times of the day or the sleep-wake schedule of animals can all include circadian rhythms. Other periods are also possible, such as 29.5 days resulting from circalunar rhythms or 12.4 hours resulting from circatidal rhythms. Oscillating genes include both core clock component genes and output genes. A core clock component gene is a gene necessary for to the pacemaker. However, an output oscillating gene, such as the AVP gene, is rhythmic but not necessary to the pacemaker.

Steven M. Reppert is an American neuroscientist known for his contributions to the fields of chronobiology and neuroethology. His research has focused primarily on the physiological, cellular, and molecular basis of circadian rhythms in mammals and more recently on the navigational mechanisms of migratory monarch butterflies. He was the Higgins Family Professor of Neuroscience at the University of Massachusetts Medical School from 2001 to 2017, and from 2001 to 2013 was the founding chair of the Department of Neurobiology. Reppert stepped down as chair in 2014. He is currently distinguished professor emeritus of neurobiology.

<i>Cycle</i> (gene)

Cycle (cyc) is a gene in Drosophila melanogaster that encodes the CYCLE protein (CYC). The Cycle gene (cyc) is expressed in a variety of cell types in a circadian manner. It is involved in controlling both the sleep-wake cycle and circadian regulation of gene expression by promoting transcription in a negative feedback mechanism. The cyc gene is located on the left arm of chromosome 3 and codes for a transcription factor containing a basic helix-loop-helix (bHLH) domain and a PAS domain. The 2.17 kb cyc gene is divided into 5 coding exons totaling 1,625 base pairs which code for 413 aminos acid residues. Currently 19 alleles are known for cyc. Orthologs performing the same function in other species include ARNTL and ARNTL2.

The frequency (frq) gene encodes the protein frequency (FRQ) that functions in the Neurospora crassa circadian clock. The FRQ protein plays a key role in circadian oscillator, serving to nucleate the negative element complex in the auto regulatory transcription-translation negative feedback-loop (TTFL) that is responsible for circadian rhythms in N. crassa. Similar rhythms are found in mammals, Drosophila and cyanobacteria. Recently, FRQ homologs have been identified in several other species of fungi. Expression of frq is controlled by the two transcription factors white collar-1 (WC-1) and white collar-2 (WC-2) that act together as the White Collar Complex (WCC) and serve as the positive element in the TTFL. Expression of frq can also be induced through light exposure in a WCC dependent manner. Forward genetics has generated many alleles of frq resulting in strains whose circadian clocks vary in period length.

Doubletime (DBT), also known as discs overgrown (DCO), is a gene that encodes the double-time protein in fruit flies. The gene was first identified and characterized in 1998 by Michael Young and his team at Rockefeller University.

<span class="mw-page-title-main">Michael Rosbash</span> American geneticist and chronobiologist (born 1944)

Michael Morris Rosbash is an American geneticist and chronobiologist. Rosbash is a professor and researcher at Brandeis University and investigator at the Howard Hughes Medical Institute. Rosbash's research group cloned the Drosophila period gene in 1984 and proposed the Transcription Translation Negative Feedback Loop for circadian clocks in 1990. In 1998, they discovered the cycle gene, clock gene, and cryptochrome photoreceptor in Drosophila through the use of forward genetics, by first identifying the phenotype of a mutant and then determining the genetics behind the mutation. Rosbash was elected to the National Academy of Sciences in 2003. Along with Michael W. Young and Jeffrey C. Hall, he was awarded the 2017 Nobel Prize in Physiology or Medicine "for their discoveries of molecular mechanisms controlling the circadian rhythm".

<span class="mw-page-title-main">Jeffrey C. Hall</span> American geneticist and chronobiologist (born 1945)

Jeffrey Connor Hall is an American geneticist and chronobiologist. Hall is Professor Emeritus of Biology at Brandeis University and currently resides in Cambridge, Maine.

Jeffrey L. Price is an American researcher and author in the fields of circadian rhythms and molecular biology. His chronobiology work with Drosophila melanogaster has led to the discoveries of the circadian genes timeless (tim) and doubletime (dbt), and the doubletime regulators spaghetti (SPAG) and bride of doubletime (BDBT).

Vrille (vri) is a bZIP transcription factor found on chromosome 2 in Drosophila melanogaster. Vrille mRNA and protein product (VRI) oscillate predictably on a 24-hour timescale and interact with other circadian clock genes to regulate circadian rhythms in Drosophila. It is also a regulator in embryogenesis; it is expressed in multiple cell types during multiple stages in development, coordinating embryonic dorsal/ventral polarity, wing-vein differentiation, and ensuring tracheal integrity. It is also active in the embryonic gut but the precise function there is unknown. Mutations in vri alter circadian period and cause circadian arrhythmicity and developmental defects in Drosophila.

<i>Drosophila</i> circadian rhythm

Drosophila circadian rhythm is a daily 24-hour cycle of rest and activity in the fruit flies of the genus Drosophila. The biological process was discovered and is best understood in the species Drosophila melanogaster. Other than normal sleep-wake activity, D. melanogaster has two unique daily behaviours, namely regular vibration during the process of hatching from the pupa, and during mating. Locomotor activity is maximum at dawn and dusk, while eclosion is at dawn.

Transcription-translation feedback loop (TTFL) is a cellular model for explaining circadian rhythms in behavior and physiology. Widely conserved across species, the TTFL is auto-regulatory, in which transcription of clock genes is regulated by their own protein products.

dClock (clk) is a gene located on the 3L chromosome of Drosophila melanogaster. Mapping and cloning of the gene indicates that it is the Drosophila homolog of the mouse gene CLOCK (mClock). The Jrk mutation disrupts the transcription cycling of per and tim and manifests dominant effects.

In the field of chronobiology, the dual circadian oscillator model refers to a model of entrainment initially proposed by Colin Pittendrigh and Serge Daan. The dual oscillator model suggests the presence of two coupled circadian oscillators: E (evening) and M (morning). The E oscillator is responsible for entraining the organism’s evening activity to dusk cues when the daylight fades, while the M oscillator is responsible for entraining the organism’s morning activity to dawn cues, when daylight increases. The E and M oscillators operate in an antiphase relationship. As the timing of the sun's position fluctuates over the course of the year, the oscillators' periods adjust accordingly. Other oscillators, including seasonal oscillators, have been found to work in conjunction with circadian oscillators in order to time different behaviors in organisms such as fruit flies.

Ravi Allada is an Indian-American chronobiologist studying the circadian and homeostatic regulation of sleep primarily in the fruit fly Drosophila. He is the Edward C. Stuntz Distinguished Professor of Neuroscience and Chair of the Department of Neurobiology at Northwestern University. Working with Michael Rosbash, he positionally cloned the Drosophila Clock gene. In his laboratory at Northwestern, he discovered a conserved mechanism for circadian control of sleep-wake cycle, as well as circuit mechanisms that manage levels of sleep.

Charles J. Weitz is a chronobiologist and neurobiologist whose work primarily focuses on studying the molecular biology and genetics of circadian clocks.

References

  1. 1 2 3 "Faculty: Paul Hardin". Texas A&M University. Archived from the original on 1 May 2017. Retrieved 13 April 2017.
  2. ↑ "Life Sciences Faculty - Michael Rosbash". www.bio.brandeis.edu. Retrieved 2017-04-14.
  3. ↑ "Previous SRBR Meetings". Society for Research on Biological Rhythms. Retrieved 27 April 2017.
  4. ↑ Denlinger, David L.; J. M. Giebultowicz; David Stanley Saunders (2001). Insect timing: circadian rhythmicity to seasonality. Gulf Professional Publishing. p. 17. ISBN   978-0-444-50608-5 . Retrieved March 31, 2011.
  5. 1 2 Vitaterna M, et al. (April 1994). "Mutagenesis and Mapping of a Mouse Gene, Clock, Essential for Circadian Behavior". Science. 264 (5159): 719–725. doi:10.1126/science.8171325. PMC   3839659 . PMID   8171325.
  6. 1 2 3 Gekakis N, Staknis D, Nguyen F, Davis L, Wilsbacher D, King D, Takahashi J, Weitz C (June 1998). "Role of the Clock Protein in the Mammalian Circadian Mechanism". Science. 280 (5359): 1564–1569. doi:10.1126/science.280.5369.1564. PMID   9616112.
  7. 1 2 Muñoz E, Baler R (2003). "The Circadian E-Box: When Perfect Is Not Good Enough". Chronobiology International. 20 (3): 371–388. doi:10.1081/CBI-120022525. ISSN   0742-0528. PMID   12868535. S2CID   163389.
  8. ↑ Claridge-Chang, A.; Wijnen, H.; Naef, F.; Boothroyd, C.; Rajewsky, N.; Young, M. W. (2001-11-20). "Circadian regulation of gene expression systems in the Drosophila head". Neuron. 32 (4): 657–671. doi: 10.1016/S0896-6273(01)00515-3 . ISSN   0896-6273. PMID   11719206. S2CID   15968641.
  9. ↑ Hastings, Michael H.; Reddy, Akhilesh B.; Maywood, Elizabeth S. (2003-08-01). "A clockwork web: circadian timing in brain and periphery, in health and disease". Nature Reviews Neuroscience. 4 (8): 649–661. doi:10.1038/nrn1177. ISSN   1471-003X. PMID   12894240. S2CID   205499642.
  10. ↑ Vitaterna, Martha Hotz; King, David P.; Chang, Anne-Marie; Kornhauser, Jon M.; Lowrey, Phillip L.; McDonald, J. David; Dove, William F.; Pinto, Lawrence H.; Turek, Fred W. (1994-04-29). "Mutagenesis and Mapping of a Mouse Gene, Clock, Essential for Circadian Behavior". Science. 264 (5159): 719–725. doi:10.1126/science.8171325. ISSN   0036-8075. PMC   3839659 . PMID   8171325.
  11. ↑ Preitner, Nicolas; Damiola, Francesca; Lopez-Molina, Luis; Zakany, Joszef; Duboule, Denis; Albrecht, Urs; Schibler, Ueli (2002-07-26). "The orphan nuclear receptor REV-ERBalpha controls circadian transcription within the positive limb of the mammalian circadian oscillator". Cell. 110 (2): 251–260. doi: 10.1016/S0092-8674(02)00825-5 . ISSN   0092-8674. PMID   12150932. S2CID   15224136.
  12. ↑ Lowrey, Phillip L.; Takahashi, Joseph S. (2004-01-01). "Mammalian circadian biology: elucidating genome-wide levels of temporal organization". Annual Review of Genomics and Human Genetics. 5: 407–441. doi:10.1146/annurev.genom.5.061903.175925. ISSN   1527-8204. PMC   3770722 . PMID   15485355.
  13. ↑ Stelling, Jörg; Sauer, Uwe; Szallasi, Zoltan; Doyle, Francis J.; Doyle, John (2004-09-17). "Robustness of cellular functions". Cell. 118 (6): 675–685. doi: 10.1016/j.cell.2004.09.008 . ISSN   0092-8674. PMID   15369668. S2CID   14214978.
  14. 1 2 3 Yi-Zhong G, Hogenesch J, Bradfield C (2000). "The PAS SUPERFAMILY: Sensors of Environmental and Developmental Signals". Annu. Rev. Pharmacol. Toxicol. 40: 519–561. doi:10.1146/annurev.pharmtox.40.1.519. PMID   10836146. S2CID   36247214.
  15. ↑ Zylka M, Shearman L, Weaver D, Reppert S (June 1998). "Three Period Homologs in Mammals: Differential Light Responses in the Suprachiasmatic Circadian Clock and Oscillating Transcripts Outside the Brain". Neuron. 20 (6): 1103–1110. doi: 10.1016/S0896-6273(00)80492-4 . PMID   9655499. S2CID   14797914.
  16. ↑ Shearman L, Sriram S, Weaver D, Maywood E (May 2000). "Interacting Molecular Loops in the Mammalian Circadian Clock". Science. 288 (5468): 1013–1019. doi:10.1126/science.288.5468.1013. PMID   10807566.
  17. ↑ Hastings M, Reddy A, Maywood E (August 2003). "A clockwork web: circadian timing in brain and periphery, in health and disease". Nature. 4 (8): 649–661. doi:10.1038/nrn1177. PMID   12894240. S2CID   205499642.
  18. ↑ Bell-Pedersen D, Cassone V, Earnest D, Golden S, Hardin P, Thomas T, Zoran M (July 2005). "Circadian rhythms from multiple oscillators: lessons from diverse organisms". Nature. 6 (7): 544–556. doi:10.1038/nrg1633. PMC   2735866 . PMID   15951747.
  19. ↑ "Paul Hardin — Faculty of Genetics". genetics.tamu.edu. Retrieved 2017-04-20.
  20. ↑ Hardin, Paul E. (2011-01-01). "Molecular genetic analysis of circadian timekeeping in Drosophila". Advances in Genetics. 74: 141–173. doi:10.1016/B978-0-12-387690-4.00005-2. ISBN   9780123876904. ISSN   0065-2660. PMC   4108082 . PMID   21924977.
  21. ↑ Hutchins, Shana (19 July 2006). "CLOCK WORK: Hardin Named to First-Ever Biology Chair". Texas A&M University. Retrieved 11 April 2017.
  22. ↑ "Moores Professorship—Past Winners". University of Houston. Retrieved 11 April 2017.
  23. ↑ "The Prize Winners". Aschoff and Honma Memorial Foundation. Retrieved 11 April 2017.
This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.