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Chromosome constitution of a hybrid between East African Buffalo (Syncerus caffer caffer) and Dwarf Forest Buffalo (Syncerus caffer nanus)

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Chromosome constitution of a hybrid between East

African Buffalo (Syncerus caffer caffer) and Dwarf

Forest Buffalo (Syncerus caffer nanus)

Edmond Cribiu, C.P. Popescu

To cite this version:

(2)

NOTE

Chromosome constitution of

a

hybrid

between East African

Buffalo

(Syncerus

caffer

caffer)

and Dwarf Forest Buffalo

(Syncerus caffer nanus)

E. P. CRIBIU C. P. POPESCU

Jeanine BOSCHER

Laboratoire de Cytogénétique UNGEIA-LN.R.A.,

Centre national de Recherches zootechniques, LN.R.A., .,

F 78350 Jouy-en-Josas (Prance)

Summary

The chromosome constitution of a male hybrid of first backcross between a female Fi

East African X Dwarf African Buffalo (Syncerus cafler cagey X Syncerus catfer nanus) and a

male Dwarf Forest Buffalo (Syncerus cagey nanus) had a chromosome number of 53 : zi

acro-centric pairs, 2

unpaired

acrocentrics, 3 meta-submetacentric pairs, I

unpaired

submetacentric and I acrocentric XY sex chromosome pair. The

R-banding

pattern shows that the chromo-somic difference between the subspecies catfer (2n = 54) and nanus (2n ! 52) is due to a centric fusion between two acrocentric pairs.

Karyotypes

of the two

subspecies

of African

Buffalo,

East African

(Syncerus

cage

7

ca f e

y

)

and Dwarf Forest

(Syncevus caffer nanus),

have

already

been described

(W

URS

T

F

R

and

BE

NIRS

C

HKE

,

I

g6

7

;

BRICH rUr and

F

I

SO

HER

,

1967

and HECK et

al.,

19

68).

The Dwarf Forest

type

had 54

chromosomes,

among which 3 autosomal

pairs

were meta-submetacentric and 23 were

acrocentric,

with the X and Y

being

acrocentric. When

compared

to the

karyotype

of Dwarf Forest

Buffalo,

the

East

African Buffalo demonstrated 52 chromosomes with one submetacentric

pair

instead of two acrocentric

pairs.

The

present report

describes the chromosome constitution of a male

hybrid

of first backcross between a female FI and a male Dwarf Forest Buffalo. The

(3)
(4)

slaugh-tered in

April 19

8

0

.

It has

recently

been included in a

study

for

heredity

of

coat colour variation

by

l,auv!xGN! and R!ErrvoisE

(ig8o).

For chromosome

observations,

a blood

sample

was obtained from the

jugular

vein and cultivated

according

to the method of DE GROUCHY et al.

(ig6

¢

);

R-banding

was achieved

by

the

technique

of DUTRILLAUX et al.

(z

973

).

The number of chromosomes in the

hybrid

is 53, among which a

submeta-centric and two acrocentrics are not

paired.

All other chromosome

pairs

are

homomorphic

except

the XY sex chromosome

pair.

Two acrocentric

pairs

exhibit

large

small arms

(fig.

i,

a).

By

using R-banding technique,

all chromosome

pairs

could be identified.

R-banding

pattern

of !

and q arms of the

unpaired

submetacentric chromosome is characteristic of the two

unpaired

acrocentric autosomes

(fig.

I,

b).

It is obvious that the

unpaired

submetacentric chromosome

originated

from

the East African

type

whereas the two

unpaired

acrocentric autosomes were

derived from the Dwarf Forest

type.

In

regard

to the

karyotype

evolution of the two

subspecies

of African

Buffalo,

it could be

suggested

that the Dwarf

type

with 2n = 54occured first and

during

evolution,

the East

African type

should have

developed by

Robertsonian fusion

of two acrocentric

pairs.

Received for publication in novembey ig8o.

Résumé

Le

caryotype

d’un

hybride

entre le

Buffle

Africain

(Syncerus

caffer

caffer)

et le

Bu!e

nain

(Syncerus

caffer

nanus)

Le caryotype d’un mâle, produit de croisement de retour d’une femelle hybride Fi Buffle Africain X Buffle nain (Syncevus caffer caffer X Syncevus caffer nanus) et d’un Buffle nain mâle

(Syncerus caffer nanus) est composé de 53chromosomes : zr paires

acrocentriques,

2chromosomes acrocentriques non appariés, 3 paires méta-submétacentriques, i chromosome submétacentrique

et 2 chromosomes sexuels X et Y acrocentriques. Le marquage R a montré que la différence

de caryotype de ces deux sous-espèce est due à une fusion centrique entre deux

paires

de

chro-mosomes acrocentriques.

References

DE GROUCHY J., Rouairr M., PASSAGE ?;., 1964. Microtechnique pour 1’6tude des

chromo-somes humains à partir d’une culture de leucocytes sanguins. Ann. Genet., 7, q5. D

U T RILL A

UX B., LAURENT M., RETURIOUC J., ZaEJ!uN! J., 1973. Coloration pour 1’acridi!le orange de chromosome préalablement trait6s par le 5 bromodeoxyuridine (B.U.D.R.). C. R. Acad. Sci. (Paris), 276, 3179-3181.

HECK H. D., WuRS2!x D. H., BENIRSCHKE K., 1968. Chromosome study of numbers of the subfamilies Capriuae and Bovidae: the muskox, ibec, aoudad, Congo buffalo and Gaur. Z. Saiigetievk, 33, 172-179.

LnuvE R G N

E J. J., RBNVOISB C., 1980. Hérédité des variations de couleur du

pelage

du Buffle africain (Syncerus caffer). Ann. Génét. Sit. Anim., 12, 1-7.

Ur.sxicx F., FISCHER M., 1967. The chromosomes of the Asiatic buffalo (Bubalus bubalis) and the African buffalo (Syncevus caJfev). Z. Tievz. Ziichtbiol., 83, 219-223.

W UR STE R

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