Showing posts with label fossil. Show all posts
Showing posts with label fossil. Show all posts

Friday, May 15, 2009

Molecular evidence for the hadrosaur B. canadensis as an outgroup to a clade containing the dinosaur T. rex and birds

Molecular analysis of collagen sequences from an 80 million year old hadrosaur B. canadensis and a 68 million year old dinosaur T. rex suggest that the two dinosaurs belong to a clade to the exclusion of birds [1,2,3].  However, well-established morphological analyses of fossils show that T. rex is more closely related to birds than it is to the ornithischian hadrosaur B. canadensis [4].  The molecular analyses were based on the molecular clock paradigm, which is known to be contradicted by fossil sequences [5,6].  It is therefore necessary to reevaluate the molecular data independent of the molecular clock paradigm. 

Here, I analyzed all the collagen sequences reported for B. canadensis and T. rex.  There are a total of four peptides whose sequences are known in the two dinosaurs and extant chicken.  But, only one of these is informative as the other three are identical among the three species.  For this single informative 18 amino acid peptide (GLPGESGAVGPAGPPGSR), I compared its sequence from all extant species including birds, reptiles, amphibians, fishes, and mammals where the sequence information is available (Table 1).  The data show that T. rex is identical to G. gallus whereas B. canadensis differs from T. rex and G. gallus at residue position 15.  An Ile residue at this position is completely conserved in all extant species of mammals, birds, and reptiles.  And yet, B. canadensis has a Pro at this position.  From the Dayhoff’s PAM (accepted point mutation) matrix [7], a change from Ile to Pro or vice versa is highly uncommon.  Furthermore, not a single extant species from mammals, birds, reptiles, amphibians, and fishes (19 species analyzed) has a Pro at this position.

These molecular data therefore suggest strongly that B. canadensis is an outgroup to a clade containing T. rex and birds, fully consistent with the well-established phylogeny based on morphological analyses of fossils [4].  The unusual change from a conserved Ile to a Pro also show that B. canadensis is genetically more distant to the outgroup fish than extant birds and reptiles, confirming the previous observation that ancient fossil specimens of extinct species are more distant to a simpler outgroup than extant sister species [5,6].  Thus, fossil sequences consistently contradict the molecular clock paradigm and would inevitably lead to absurd conclusions if analyzed under the assumptions of that paradigm.  

Reference:

1. Schweitzer MH, Zheng W, Organ CL, Avci R, Suo Z, et al. (2009) Biomolecular characterization and protein sequences of the Campanian hadrosaur B. canadensis. Science 324: 626-631.

2. Asara JM, Schweitzer MH, Freimark LM, Phillips M, Cantley LC (2007) Protein Sequences from Mastodon and Tyrannosaurus Rex Revealed by Mass Spectrometry. Science 316: 280-285.

3. Asara JM, Schweitzer MH (2008) Response to Comment on "Protein sequences from mastodon and Tyrannosaurus rex revealed by mass spectrometry". Science 319: 33.

4. Pisani D, Yates AM, Langer MC, Benton MJ (2002) A genus-level supertree of the Dinosauria. Proc Biol Sci 269: 915-921.

5. Huang S (2008) Ancient fossil specimens are genetically more distant to an outgroup than extant sister species are. Riv Biol 101: 93-108.

6. Green RE, Malaspinas AS, Krause J, Briggs AW, Johnson PL, et al. (2008) A complete Neandertal mitochondrial genome sequence determined by high-throughput sequencing. Cell 134: 416-426.

7. Dayhoff MO (1978) Atlas of protein sequence and structure. Washington, D.C.: National Biomedical Research Foundation.


Table 1. Sequence alignment of a peptide from collagen alpha 2 type 1.

 

B. Canadensis         GLPGESGAVGPAGPPGSR

 

T. rex                ..............I...

G. gallus             ..............I...

T. guttata            .P............I...

S. camelus            .P............I...

 

A. mississippiensis   ...........V..I...

A. carolinensis       .A.........S..I...

 

H. sapiens            .P......A..T..I...

M. mulluta            .P......A..T..I...

B. taurus             .P......A..T..I...

M. americanum         .P..Q...A..T..I...

L. afiricana          .P..Q...A..T..I...

M. musculus           .T......A..S..I...

R. norvegicus         .P......A..S..I...

E. telfairi           .P..Q...A..T.SI...

 

M. domestica          .P.........T.SI...

 

X. levis              .T......A..F..L.P.

X. tropicalis         .A......A..L.AL.P.

R. catesbeiana        .A.....GA..H.PS...

 

D. rerio              .N..PA..A.AQ..I.A.

O. mykiss             .NS.PA.SA.SQ.AI.A.

P. olivaceus          .IN.VA..S.VQ.AV.A.

 



Monday, May 11, 2009

On the collagen sequence of the Campanian hadrosaurs (duck-billed dinosaur) B. Canadensis

Collagen sequences from an 80 million year old dinosaur were published recently. 

Schweitzer et al., 2009, Biomolecular Characterization and Protein Sequences of the Campanian Hadrosaur B. Canadensis, Science, 5927, pp. 626 - 631

Below I analyzed the 8 peptide sequences reported.  My analysis showed that B. Canadensis is an outgroup to a T.rex-bird clade, consistent with morphological data but different from the conclusion of Schweitzer et al.  Also, the analysis confirmed the major findings of my early fossil sequence paper.   

1

GLTGPIGPPGPAGAPGDKGEAGPSGPPGPTGAR

100% identical to mouse

 

2

GSAGPPGATGFPGAAGR

100% T. rex, 100% chicken, and 100% mammals, 17/17, 100% mammut

 

3

GATGAPGIAGAPGFPGAR

100% T. rex, 100% chicken, 100% rana. 18/18, 17/18 homo, 17/18 mammut

 

4

GETGPAGPAGPPGPAGAR

100% Chicken, 17/18 rana, 17/18 homo, 16/18 mus, 13/18 match in mammut,

 

5

GATGAPGIAGAPGFPGAR

100% T. rex, 100% chicken, 100% frog/newt/rana, 17/18 homo, 17/18 mammut

 

6

GPSGPQGPSGAPGPK

100% Chicken, 100% rat, and 100% opossum. 14/15 mus, 13/15 homo, 12/15 mammut

 

7

GSNGEPGSAGPPGPAGLR

Collagen a2(1)

100% Chicken, and 17/18 Taeniopygia guttata, 15/18, homo, 13/18 mammut

 

8

GLPGESGAVGPAGPPGSR

Collagen a2(1)

17/18 T. rex, 17/18 chicken, 16/18, Taeniopygia, 17/18 between chicken and Taeniopygia.  Much less to others.  18/18 between chicken and T. rex. 

 

Some questions:

 

1.  Is B. canadensis more related to T. rex than chicken is? 

No.  It is equidistant to chicken and T. rex.  And chicken is closer to T. rex than Bc is to T. rex.  The informative peptide in this case is #8.  Of 4 peptides whose sequences are known in Bc, Tr, and chicken, three (peptide #2, #3, #5) are non informative as they are identical among the three species.

 

2.  Is B. canadensis more related to birds than to other animals? 

Yes, informative peptides 4, 7, 8 show B. canadensis more similar to chicken than to frog or mammals or any other. 

 

3.  Is B. canadensis more related to bird than T. rex is?

The only informative peptide is #8.  For this peptide, Tr is 18/18 to chicken and 17/18 to Tg (Taeniopygia guttata).  Bc is 17/18 to chicken, and 16/18 to Taeniopygia.  So, Tr is more related to birds than Bc is.

 

4.  Is B. canadensis more distant to the outgroup frog than bird/mammal are?

Not a single informative peptide.   Seven of the 8 peptides are not unique to Bc.  Peptide 8 is unique but not very conserved in extant animals.

 

5.  Is the distance between B. canadensis and mammut greater than that between extant birds and extant mammals?

Yes.  Of 6 informative peptides (1-6 of collagen A1t1), 4 and 6 show that distance between Bc and mammut (25/33) is greater than that between birds and mammals (29/33).  The distance between extant birds and mammut is also greater than between extant birds and extant mammals.  This result confirms the previous finding on the distance between Tr and mammuts. Only the MGD but not the molecular clock hypothesis can predict such result.


Conclusion: Bc is the outgroup to a Tr-bird clade

Schweitzer et al stated: “However, on the basis of well-established morphological analyses (25), we predict that T. rex is more closely related to birds than it is to the ornithischian hadrosaur B. canadensis.” 25. D. Pisani et al., Proc. R. Soc. London Ser. B Biol. Sci. 269, 915 (2002).

Yet their molecular analysis based on certain statistical methods suggest that the two dinosaurs belong to a clade to the exclusion of birds.  Such a conclusion is false because it is based on the completely mistaken paradigm of molecular clock and neutral theory.  So, my analysis shows Bc as the outgroup to a clade containing birds and Tr.  This conclusion is more consistent with morphological analysis.  The fact that Tr is closer to a bird Gg than a bird Gg is to another bird Tg may be due to the fact that Tr has 60 million years less time to mutate than extant birds are, or that Tg had a different dinosaur ancestor.  


Tuesday, April 17, 2007

Ancient fossil specimens of extinct species are more distant to an outgroup than extant sister species are

Shi Huang,Ph.D.
Program on Cancer Genetics and Epigenetics
The Burnham Institute for Medical Research
10901 North Torrey Pines Roads
La Jolla, CA 92037



Abstract
The molecular clock hypothesis was proposed 45 years ago to explain the remarkable molecular evolution phenomenon that sister species are roughly equally distant to an outgroup. The hypothesis predicts that ancient specimens cannot possibly be more distant to an outgroup than extant sister species are. However, my analysis of the published DNA/peptide sequences of fossil specimens of extinct species contradicts this prediction. Neanderthals are significantly more distant to chimpanzees and gorillas than modern humans are. Dinosaurs are significantly more distant to frogs than extant birds are. Mastodons are significantly more distant to opossums than other placental mammals are.


Ancient fossil specimens can be used to test the molecular clock hypothesis or the Darwinian gradual mutation model. The hypothesis predicts that ancient specimens cannot possibly be more distant to an outgroup than extant sister species are. They should be either equally related or more related to an outgroup than extant sister species are, because they have had less time to accumulate mutations. Extant humans and chimpanzees are equally distant to the outgroup gorillas. Ancient fossil specimens of humans cannot possibly be more distant to gorillas than extant chimpanzees are, if the molecular clock hypothesis is true.

I first analyzed the published DNA sequences of Neanderthals. Neanderthals are a group of extinct hominids that inhabited Europe and western Asia from about 400,000 to 30,000 years ago. Analysis of molecular genetic variation in the mitochondrial and nuclear genomes of living human populations have generally supported the view that Neanderthals were completely replaced by modern humans without contributing any genes (Armour et al., 1996; Hammer et al., 1998; Stringer and Andrews, 1988; Tishkoff et al., 1996; Vigilant et al., 1991). However, these analysis rely on assumptions whose validity has been questioned (Templeton, 1992; Wolpoff, 1989). In contrast to the replacement model, the multiregional model that is largely based on fossil evidence suggests that Neanderthals were the ancestors of modern Europeans (Wolpoff et al., 2000). Influenced by the gradual mutation model of speciation, sequence analysis of Neanderthal DNAs are commonly thought to represent the best approach to resolve the issue of whether Neanderthals contributed some genes to modern humans. In 1997, a segment of the mitochondrial DNA (mtDNA) of Neanderthals was sequenced and was found to be distinct from modern humans (Krings et al., 1997). Subsequently, mtDNA sequences have been retrieved from eleven additional Neanderthal specimens. Although some of these sequences are extremely short, they are all more closely related to one another than to modern human mtDNAs (Orlando et al., 2006). This fact has been interpreted to mean that Neanderthals contributed no mtDNA to present-day humans. Recently, the Neanderthal nuclear genomic DNAs have been sequenced (Green et al., 2006; Noonan et al., 2006). The data however suggests that there may be some degree of gene flow between modern humans and Neanderthals (Green et al., 2006).

If Neanderthals were alive today, they and living modern human would be equally distant from the outgroup chimpanzees. If the gradual molecular clock hypothesis is true, ancient Neanderthals of 40,000-100,000 years ago cannot possibly be significantly more distant to chimpanzees than extant humans are. I first examined five published Neanderthal mitochondrial hyper-variable region I sequences that are longer than 300 nucleotides. By searching against all chimpanzee sequences (1000 sequences) in the NCBI database, the average similarity score between Neanderthal and chimpanzee is 235 for the most related and 63 for the least related. For each Neanderthal sequence, I selected a closely related human sequence of equal length and used it to search the chimpanzee sequences. The average score between human and chimpanzee is 269 for the most related and 74 for the least related. I also determined the relationship with chimpanzees for five African tribes and six Australian DNAs of 8000-60000 years old. All of these show higher similarities with chimpanzees than the Neanderthals do, although ancient Australian DNAs seem to be slightly more distant to chimpanzees than living humans do. So, modern human DNAs are more related to chimpanzees than the Neanderthals are.

I next studied the statistical significance of this finding. If the finding represents random noise of sequence comparisons, it should be easy to find some human sample sequences that show less identity with chimpanzees than Neanderthals do. I examined 11 Neanderthal hyper-variable region 1 sequences ranging in size from 31 bp to 379 bp. For each of these sequences, I identified a distinct modern human sequence of equal length that shows the highest identity with the Neanderthal sequence. These Neanderthal-like sequences have the best chance of being equally related to chimpanzees as the Neanderthals are. They are all more distant to chimpanzees than the Cambridge Reference sequence of human mitochondrial DNA. They are in fact more distant to chimpanzees than other human sequences that are less similar to Neanderthals. For example, for the first reported Neanderthal sequence AF011222 (379 bp), the most closely related human sequence is AY957203 (94% identity) and the least related is AY210529 (90% identity). But AY957203 is more distant to chimpanzees than AY210529 is.

Of the 11 independent sequences of hyper-variable region I, 9 showed more similarity between modern humans and chimpanzees than between Neanderthals and chimpanzees and 2 (both of 31 bp in length) showed equal similarity. The observation of 9 cases of more similarity between humans and chimpanzees against 0 case of more similarity between Neanderthals and chimpanzees is highly significant by Chi square test (Chi-square = 6, P<0.025, square =" 13.33,">>0.05). The result therefore confirms the well-established molecular equidistance phenomenon where chimpanzees and humans are equidistant to gorillas. I next examined all available Neanderthal mitochondrial sequences that are long enough to be informative for my analysis (longer than 30 bp of homology with gorillas). These included 6 hyper-variable region I and 2 hyper-variable region II sequences. For each Neanderthal sequence, a closely related chimpanzee sequence of equal length was selected. Each Neanderthal sequence and its corresponding chimpanzee sequence were used to obtain a best BLAST similarity score with gorilla non-nuclear mitochondrial sequences in the Genbank. All 8 comparisons showed greater similarity between chimpanzees and gorillas than between Neanderthals and gorillas (P <>1 million years) (Ho and Larson, 2006). Based on the pedigree mutation rate in the mitochondrial genome, the human race is only 6000 years old. The high mutation rate allows replacement of variants with new variants possible within a short time frame. It is thus well established that most genetic variants present in a living species of today will not be present in the same species a million years from now. Thus periodic replacement of variants may be an inherent phenomenon of evolution.

The molecular equidistance phenomenon is an extremely consistent and solid fact of molecular evolution. Some purported exceptions to this phenomenon are not based on sound statistical analysis and presuppose the validity of the molecular clock hypothesis. The greater distance of ancient Neanderthals/dinosaurs/mastodons to an outgroup relative to their extant sister species would mean the same for living Neanderthals/dinosaurs/mastodons if the clock hypothesis is true, which would represent the first statistically significant violation of the molecular equidistance phenomenon. Either the clock hypothesis is not valid and so the molecular equidistance phenomenon would hold. Or the molecular equidistance phenomenon must be false and so the clock hypothesis would hold. Since the molecular equidistance phenomenon holds in all cases analyzed while the clock hypothesis remains unproven, it is much less costly to a coherent story of the whole to consider the clock hypothesis to be false.



Acknowledgments:
I thank Dr. John Hawks for critical reading of the manuscript. This work was supported by NIH (RO1 CA 105347).

Literature cited:

Armour, J. A., Anttinen, T., May, C. A., Vega, E. E., Sajantila, A., Kidd, J. R., Kidd, K. K., Bertranpetit, J., Paabo, S., and Jeffreys, A. J. (1996). Minisatellite diversity supports a recent African origin for modern humans. Nat Genet 13, 154-160.
Asara, J. M., Schweitzer, M. H., Freimark, L. M., Phillips, M., and Cantley, L. C. (2007). Protein Sequences from Mastodon and Tyrannosaurus Rex Revealed by Mass Spectrometry. Science 316, 280-285.
Green, R. E., Krause, J., Ptak, S. E., Briggs, A. W., Ronan, M. T., Simons, J. F., Du, L., Egholm, M., Rothberg, J. M., Paunovic, M., and Paabo, S. (2006). Analysis of one million base pairs of Neanderthal DNA. Nature 444, 330-336.
Hammer, M. F., Karafet, T., Rasanayagam, A., Wood, E. T., Altheide, T. K., Jenkins, T., Griffiths, R. C., Templeton, A. R., and Zegura, S. L. (1998). Out of Africa and back again: nested cladistic analysis of human Y chromosome variation. Mol Biol Evol 15, 427-441.
Ho, S. Y. W., and Larson, G. (2006). Molecular clocks: when times are a-changin'. Trends in Genetics 22, 79-83.
Krings, M., Capelli, C., Tschentscher, F., Geisert, H., Meyer, S., von Haeseler, A., Grossschmidt, K., Possnert, G., Paunovic, M., and Paabo, S. (2000). A view of Neandertal genetic diversity. Nat Genet 26, 144-146.
Krings, M., Stone, A., Schmitz, R. W., Krainitzki, H., Stoneking, M., and Paabo, S. (1997). Neandertal DNA sequences and the origin of modern humans. Cell 90, 19-30.
Noonan, J. P., Coop, G., Kudaravalli, S., Smith, D., Krause, J., Alessi, J., Chen, F., Platt, D., Paabo, S., Pritchard, J. K., and Rubin, E. M. (2006). Sequencing and Analysis of Neanderthal Genomic DNA. Science 314, 1113-1118.
Orlando, L., Darlu, P., Toussaint, M., Bonjean, D., Otte, M., and Hanni, C. (2006). Revisiting Neandertal diversity with a 100,000 year old mtDNA sequence. Curr Biol 16, R400-402.
Stringer, C. B., and Andrews, P. (1988). Genetic and fossil evidence for the origin of modern humans. Science 239, 1263-1268.
Templeton, A. R. (1992). Human origins and analysis of mitochondrial DNA sequences. Science 255, 737.
Tishkoff, S. A., Dietzsch, E., Speed, W., Pakstis, A. J., Kidd, J. R., Cheung, K., Bonne-Tamir, B., Santachiara-Benerecetti, A. S., Moral, P., and Krings, M. (1996). Global patterns of linkage disequilibrium at the CD4 locus and modern human origins. Science 271, 1380-1387.
Vigilant, L., Stoneking, M., Harpending, H., Hawkes, K., and Wilson, A. C. (1991). African populations and the evolution of human mitochondrial DNA. Science 253, 1503-1507.
Wolpoff, M. H. (1989). Multiregional evolution: the fossil alternative to Eden. (Edinburgh: Edinburgh University Press).
Wolpoff, M. H., Hawks, J., and Caspari, R. (2000). Multiregional, not multiple origins. Am J Phys Anthropol 112, 129-136.