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Clinical Biochemistry of Domestic Animals (Sixth Edition) - UMK ...

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II. Anterior Lobe and Intermediate Lobe<br />

583<br />

Pig LPICPSGAVNCQMSLRDLFDRAVILSHYIHNLSSEMFNEFDKRYAQGRGFITKAINSCHTSSLSTPEDKE 70<br />

Horse ------------V---E---------------------------------V-------------------<br />

Dog ------------V---------------------------------------------------------<br />

Cat ------------V--------------------------------------------------P------<br />

Goat T-V--N-PG---V----------MV----------------------K-Y--MAL--------P------<br />

Sheep T-V--N-PGD--V----------MV----------------------K----MAL--------P------<br />

Cattle T-V--N-PG---V----------MV-----D----------------K----MAL--------P------<br />

Human -----G--AR--VT---------V-------------S------TH-------AI--------A------<br />

Rat --V-SG- D--TP-PE----V-M------T-YTD--I----Q-V-D-E--A-A--D-P----A------<br />

Mouse ----SA- D--T---E----V--------T-YTD--I----Q-V-D-E-MV-V--D-P----A------<br />

* * * ** * **** * ***** * ** **** * * * **** ******<br />

Pig QAQQIHHEVLLNLILRVLRSWNDPLYHLVTEVRGMQEAPDAILSRAIEIEEQNKRLLEGMEKIVGQVHPG 140<br />

Horse --------D--------------------S---------E----K--------R-------------Q-R<br />

Dog --------D--------------------------------------------R----------------<br />

Cat --------D---V---------------------LH-----------------R----------H-----<br />

Goat ----T-----MS---GL------------------KGV-------------E---------M-F---I--<br />

Sheep ----T-----MS---GL------------------KGV-------------E---------M-F---I--<br />

Cattle ----T-----MS---GL------------------KG--------------E---------M-F---I--<br />

Human ----MNQKDF-S--VSI-----E----------------E----K-V-----T--------L--S----E<br />

Rat ---KVPP--------SLVH------FQ-I-GLG-IH------I---K------------I---IS-AY-E<br />

Mouse --LKVPP--------SLVQ-SSDPLFQ-I-GVG-I----EY-----K-------Q----V---IS-AY-E<br />

** * * * * * * * * * **** **** * * * *<br />

Pig IKENEVYSVWSGLPSLQMADEDTRLFAFYNLLHCLRRDSHKIDNYLKLLKCRIIYDSNC 199<br />

Horse ----------------------S------------------------------V-----<br />

Dog -R---------------------------------------------------V-----<br />

Cat VR--------------------S--------------------S---------V-----<br />

Goat A-ET-P-P---------TK--EA-HS-------------S---T-----N-----NN--<br />

Sheep A-ET-P-P---------TK---A-HS-------------S---T-----N-----NN--<br />

Cattle A--T-P-P---------TK---A-YS-------------S---T-----N-----NN--<br />

Human T-EN-I-P-------------ES--S-Y--------------------------HNN--<br />

Rat A-GN-I-L---Q-----GV--ESKDL----NIR--------V-----F-R-Q-VHKN--<br />

Mouse A-GNGI-F---Q-----GV--ESKILSLRNTIR----H---V--F--V-R-Q-AHQN--<br />

* *** ***** ** **** * * * ** * * * **<br />

FIGURE 18-13 Sequence comparison <strong>of</strong> PRL. See the legend for Figure 18-6 .<br />

Cat<br />

Dog<br />

Horse<br />

Pig<br />

Goat<br />

Sheep<br />

Cattle<br />

Human<br />

Mouse<br />

Rat<br />

It should be kept in mind that the reference values for<br />

plasma IGF-I concentrations in the dog are breed ( body<br />

size) dependent.<br />

2 . Prolactin<br />

a . Gene Expression<br />

Prolactin (PRL) is encoded by a single gene in humans. In<br />

nonprimates, a family <strong>of</strong> PRL-related genes is found and only<br />

one gene encoding GH. In the rat, a PRL family <strong>of</strong> at least<br />

24 related genes can be found including the placental lactogens,<br />

proliferans, and PRL-like proteins (PLPs) ( Alam et al. ,<br />

2006 ). In the cow, an expanded PRL family also has been<br />

found; however, its members are not orthologous with members<br />

<strong>of</strong> the mouse and rat PRL family genes ( Soares, 2004 ).<br />

Expansion <strong>of</strong> the PRL family does not exist in the dog.<br />

The appearance <strong>of</strong> specific PRL-producing lactotropes<br />

is one <strong>of</strong> the latest events in pituitary development. It has<br />

been proposed that lactotropes arise from somatotropes or<br />

at least a common progenitor cell, the somatomammotrope<br />

( Burrows et al. , 1999 ). In chicken, however, evidence is<br />

presented that lactotropes do not differentiate from somatotropes<br />

during embryonic development ( Fu et al. , 2004 ). In<br />

mouse pituitaries, mammosomatotropes represent only 5%<br />

to 6% <strong>of</strong> somatotropes ( Villalobos et al. , 2004 ).<br />

The Pit-1 transcription factor is a prerequisite factor<br />

for PRL expression, as it is for GH and TSH. In the PRL<br />

gene Pit-1 acts in synergy with an estrogen nuclear receptor<br />

(ER) at a distal enhancer site, with two ETS-domaincontaining<br />

factors (Ets-1 and ERF) and the Pitx1 and Pitx2<br />

transcription factors ( Dasen and Rosenfeld, 2001 ). The<br />

expression and release <strong>of</strong> PRL are under tonic dopaminergic<br />

inhibitory control. No consensus exists on the identity <strong>of</strong><br />

physiologically relevant PRL releasing factors. In extracts<br />

<strong>of</strong> the bovine posterior pituitary, a PRL-releasing factor was<br />

found ( Hashizume et al. , 2005 ). The melanocortin peptide<br />

γ 3-MSH also stimulates PRL expression ( Langouche et al. ,<br />

2004 ), whereas a variety <strong>of</strong> factors are found that stimulate<br />

PRL release, such as PRL-releasing peptide (PrRP), TRH,<br />

oxytocin, VIP, angiotensin II, PACAP, and intermedin and<br />

may also stimulate PRL gene expression.<br />

The PRL gene, like the GH gene, has five exon areas.<br />

In the pituitary, a promoter upstream <strong>of</strong> the Cap site in<br />

exon 1b is used, outside the pituitary expression <strong>of</strong> PRL is<br />

regulated by a second promoter upstream <strong>of</strong> exon 1a initially<br />

described for PRL expression in decidua and lymphocytes<br />

( Gerlo et al. , 2006 ; G<strong>of</strong>fin et al. , 2002 ).<br />

b . (Pro)hormone<br />

Prolactin (PRL) is synthesized as a single polypeptide,<br />

which, after cleavage <strong>of</strong> the signal peptide, has a molecular<br />

weight <strong>of</strong> approximately 23,000 daltons and three intrachain<br />

disulfide bridges. There is a good deal <strong>of</strong> variability in the<br />

sequences <strong>of</strong> PRL from different species. The rat and mouse<br />

PRL are most distinct and differ from the other sequences<br />

at about 40% <strong>of</strong> all amino acid residues ( Fig. 18-13 ).

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